U.S. patent application number 10/362719 was filed with the patent office on 2004-01-29 for curable fluoropolymer, curable resin composition containing the same, and antireflection film.
Invention is credited to Araki, Takayuki, Ohashi, Mihoko, Shimizu, Tetsuo, Tanaka, Yoshito.
Application Number | 20040019176 10/362719 |
Document ID | / |
Family ID | 27344456 |
Filed Date | 2004-01-29 |
United States Patent
Application |
20040019176 |
Kind Code |
A1 |
Araki, Takayuki ; et
al. |
January 29, 2004 |
Curable fluoropolymer, curable resin composition containing the
same, and antireflection film
Abstract
There are provided a curable fluorine-containing polymer which
can realize a high hardness by photo-curing while maintaining a low
refractive index, an antireflection film possessing improved
scratch resistance and abrasion resistance while maintaining a
reflection reducing effect, and an antireflection-treated article
provided with such an antireflection film. The curable
fluorine-containing polymer has a number average molecular weight
of from 500 to 1,000,000 and is represented by the formula (1):
A.paren close-st.M.paren close-st. (1) in which the structural unit
M is a structural unit derived from a fluorine-containing ethylenic
monomer and represented by the formula (M): 1 wherein X.sup.1 and
X.sup.2 are the same or different and each is H or F; X.sup.3 is H,
F, CH.sub.3 or CF.sub.3; X.sup.4 and X.sup.5 are the same or
different and each is H, F or CF.sub.3; Rf is an organic group in
which 1 to 3 of Y.sup.1 (Y.sup.1 is a monovalent organic group
having 2 to 10 carbon atoms and an ethylenic carbon-carbon double
bond at its end) are bonded to a fluorine-containing alkyl group
having 1 to 40 carbon atoms or a fluorine-containing alkyl group
having 2 to 100 carbon atoms and ether bond; a is 0 or an integer
of from 1 to 3; b and c are the same or different and each is 0 or
1, the structural unit A is a structural unit derived from a
monomer copolymerizable with the fluorine-containing ethylenic
monomer represented by the formula (M), and the structural unit M
and the structural unit A are contained in amounts of from 0.1 to
100 % by mole and from 0 to 99.9 % by mole, respectively.
Inventors: |
Araki, Takayuki; (Osaka,
JP) ; Ohashi, Mihoko; (Osaka, JP) ; Tanaka,
Yoshito; (Osaka, JP) ; Shimizu, Tetsuo;
(Osaka, JP) |
Correspondence
Address: |
SUGHRUE MION, PLLC
2100 PENNSYLVANIA AVENUE, N.W.
WASHINGTON
DC
20037
US
|
Family ID: |
27344456 |
Appl. No.: |
10/362719 |
Filed: |
February 26, 2003 |
PCT Filed: |
August 28, 2001 |
PCT NO: |
PCT/JP01/07344 |
Current U.S.
Class: |
528/242 |
Current CPC
Class: |
Y10T 428/3154 20150401;
C08F 290/04 20130101; C08F 214/18 20130101; C08F 8/00 20130101;
C09D 127/12 20130101; C08F 8/14 20130101; C08F 16/32 20130101; C08F
8/00 20130101; C08F 14/18 20130101 |
Class at
Publication: |
528/242 |
International
Class: |
C08G 004/00 |
Foreign Application Data
Date |
Code |
Application Number |
Aug 29, 2000 |
JP |
2000-259583 |
Oct 3, 2000 |
JP |
2000-303723 |
Mar 14, 2001 |
JP |
2001-73025 |
Claims
1. A curable fluorine-containing polymer which has a number average
molecular weight of from 500 to 1,000,000 and is represented by the
formula (1): M.paren close-st.A.paren close-st. (1) in which the
structural unit M is a structural unit derived from
fluorine-containing ethylenic monomer and represented by the
formula (M): 90wherein X.sup.1 and X.sup.2 are the same or
different and each is H or F; X.sup.3 is H, F, CH.sub.3 or
CF.sub.3; X.sup.4 and X.sup.5 are the same or different and each is
H, F or CF.sub.3; Rf is an organic group in which 1 to 3 of Y.sup.1
(Y.sup.1 is a monovalent organic group having 2 to 10 carbon atoms
and an ethylenic carbon-carbon double bond at its end) are bonded
to a fluorine-containing alkyl group having 1 to 40 carbon atoms or
a fluorine-containing alkyl group having 2 to 100 carbon atoms and
ether bond; a is 0 or an integer of from 1 to 3; b and c are the
same or different and each is 0 or 1, the structural unit A is a
structural unit derived from monomer copolymerizable with the
fluorine-containing ethylenic monomer represented by the formula
(M), said polymer comprises from 0.1 to 100% by mole of the
structural unit M and from 0 to 99.9% by mole of the structural
unit A.
2. A curable fluorine-containing polymer which has a number average
molecular weight of from 500 to 1,000,000 and is represented by the
formula (1-1): M.paren close-st.A1.paren close-st.A2.paren
close-st. (1-1) in which the structural unit M is the same
structural unit as said formula (M), the structural unit A1 is a
structural unit represented by the formula (A1): 91wherein
X.sup.11, X.sup.12 and X.sup.13 are the same or different and each
is H or F; X.sup.14 is H, F or CF.sub.3; h is 0, 1 or 2; i is 0 or
1; Rf.sup.4 is a fluorine-containing alkylene group having 1 to 40
carbon atoms or a fluorine-containing alkylene group having 2 to
100 carbon atoms and ether bond; Z.sup.1 is selected from --OH,
--CH.sub.2OH, --COOH, carboxylic acid derivative, --SO.sub.3H,
sulfonic acid derivative, epoxy group and cyano group, the
structural unit A2 is a structural unit represented by the formula
(A2): 92wherein X.sup.15, X.sup.16 and X.sup.18 are H or F;
X.sup.17 is H, F or CF.sub.3; h1, i1 and j are 0 or 1; Z.sup.2 is
H, F or Cl; Rf.sup.5 is a fluorine-containing alkylene group having
1 to 20 carbon atoms or a fluorine-containing alkylene group having
2 to 100 carbon atoms and ether bond, said polymer comprises from
0.1 to 90% by mole of the structural unit M, from 0 to 99.9% by
mole of the structural unit Al and from 0 to 99.9% by mole of the
structural unit A2 and contains from 10 to 99.9% by mole of
A1+A2.
3. The curable fluorine-containing polymer of claim 1 or 2, wherein
at least one Y.sup.1 is bonded to an end of Rf.
4. The curable fluorine-containing polymer of any of claims 1 to 3,
wherein in the formula (1) or (1-1), the structural unit M is a
structural unit M1 derived from fluorine-containing ethylenic
monomer and represented by the formula (M1): 93wherein X.sup.1 and
X.sup.2 are the same or different and each is H or F; X.sup.3 is H,
F, CH.sub.3 or CF.sub.3; X.sup.4 and X.sup.5 are the same or
different and each is H, F or CF.sub.3; Rf is an organic group in
which 1 to 3 of Y.sup.1 (Y.sup.1 is a monovalent organic group
having 2 to 10 carbon atoms and an ethylenic carbon-carbon double
bond at its end) are bonded to a fluorine-containing alkyl group
having 1 to 40 carbon atoms or a fluorine-containing alkyl group
having 2 to 100 carbon atoms and ether bond; a is 0 or an integer
of from 1 to 3; c is 0 or 1.
5. The curable fluorine-containing polymer of any of claims 1 to 3,
wherein in the formula (1) or (1-1), the structural unit M is a
structural unit M2 derived from fluorine-containing ethylenic
monomer and represented by the formula (M2): 94wherein Rf is an
organic group in which 1 to 3 of Y.sup.1 (Y.sup.1 is a monovalent
organic group having 2 to 10 carbon atoms and an ethylenic
carbon-carbon double bond at its end) are bonded to a
fluorine-containing alkyl group having 1 to 40 carbon atoms or a
fluorine-containing alkyl group having 2 to 100 carbon atoms and
ether bond.
6. The curable fluorine-containing polymer of any of claims 1 to 3,
wherein in the formula (1) or (1-1), the structural unit M is a
structural unit M3 derived from fluorine-containing ethylenic
monomer and represented by the formula (M3): 95wherein Rf is an
organic group in which 1 to 3 of Y.sup.1 (Y.sup.1 is a monovalent
organic group having 2 to 10 carbon atoms and an ethylenic
carbon-carbon double bond at its end) are bonded to a
fluorine-containing alkyl group having 1 to 40 carbon atoms or a
fluorine-containing alkyl group having 2 to 100 carbon atoms and
ether bond.
7. The curable fluorine-containing polymer of any of claims 1 to 6,
wherein Y.sup.1 is an organic group represented by the formula:
O.paren close-st..sub.dC.dbd.O).sub.e--Y.sup.2 wherein Y.sup.2 is
an alkenyl group or fluorine-containing alkenyl group having 2 to 5
carbon atoms and an ethylenic carbon-carbon double bond at an end
thereof; d and e are the same or different and each is 0 or 1.
8. The curable fluorine-containing polymer of any of claims 1 to 6,
wherein Y.sup.1 is represented by the formula:
--O(C.dbd.O)CX.sup.6.dbd.C- X.sup.7X.sup.8 wherein X.sup.6 is H, F,
CH.sub.3 or CF.sub.3; X.sup.7 and X.sup.8 are the same or different
and each is H or F.
9. The curable fluorine-containing polymer of any of claims 2 to 8,
wherein in the formula (1-1), the structural unit (A1) is
represented by the formula (A1-1): 96wherein Rf.sup.4 and Z.sup.1
are as defined in the formula (A1).
10. The curable fluorine-containing polymer of any of claims 2 to
8, wherein in the formula (1-1), the structural unit (A1) is
represented by the formula (A1-2): 97wherein Rf.sup.4 and Z.sup.1
are as defined in the formula (A1).
11. The curable fluorine-containing polymer of any of claims 2 to
10, wherein in the formula (1-1), the structural unit (A2) is a
structural unit derived from at least one monomer selected from
tetrafluoroethylene, vinylidene fluoride, chlorotrifluoroethylene
and hexafluoropropylene.
12. The curable fluorine-containing polymer of any of claims 2 to
10, wherein the polymer of the formula (1-1) comprises from 10 to
80% by mole of the structural unit M, from 1 to 60% by mole of the
structural unit A1 and from 20 to 85% by mole of the structural
unit A2 and contains from 20 to 90% by mole of A1+A2.
13. The curable fluorine-containing polymer of any of claims 1 to
12, which has a refractive index of not more than 1.40.
14. The curable fluorine-containing polymer of any of claims 1 to
13, which is soluble in at least one solvent selected from the
group consisting of ketone solvents, acetic acid ester solvents,
alcohol solvents and aromatic hydrocarbon solvents.
15. A process for preparing a curable fluorine-containing polymer
having a number average molecular weight of from 500 to 1,000,000,
which is characterized by comprising: esterifying a
fluorine-containing polymer having hydroxyl and represented by the
formula (2) N.paren close-st.B.paren close-st. (2) in which the
structural unit N is a structural unit having hydroxyl and derived
from a fluorine-containing ethylenic monomer and is represented by
the formula (N): 98wherein X.sup.1 and X.sup.2 are the same or
different and each is H or F; X.sup.3 is H, F, CH.sub.3 or
CF.sub.3; X.sup.4 and X.sup.5 are the same or different and each is
H, F or CF.sub.3; Rf.sup.1 is an organic group in which 1 to 3 of
Y.sup.5 (Y.sup.5 is hydroxyl or a monovalent organic group having 1
to 10 carbon atoms and hydroxyl) are bonded to a
fluorine-containing alkyl group having 1 to 40 carbon atoms or a
fluorine-containing alkyl group having 2 to 100 carbon atoms and
ether bond; a is 0 or an integer of from 1 to 3; b and c are the
same or different and each is 0 or 1, the structural unit (B) is a
structural unit derived from monomer copolymerizable with the
fluorine-containing ethylenic monomer having hydroxyl and
represented by the formula (N), and the structural unit N and the
structural unit B are contained in amounts of from 0.1 to 100% by
mole and from 0 to 99.9% by mole, respectively, with an unsaturated
carboxylic acid or its derivative having 3 to 10 carbon atoms (a
total number of carbon atoms including carbon atoms of Ys is from 3
to 10) and represented by the formula: HOOCR.sup.1.paren
close-st..sub.fCX.sup.6.dbd.CX.sup.7X.sup.8 wherein R.sup.1 is a
divalent organic group which has 1 to 7 carbon atoms and may be
substituted with fluorine atom; X.sup.6 is H, F, CH.sub.3 or
CF.sub.3; X.sup.7 and X.sup.8 are the same or different and each is
H or F; f is 0 or 1, said curable fluorine-containing polymer is
represented by the formula (1a): M4.paren close-st.A.paren
close-st. (1a) in which the structural unit M4 is a structural unit
derived from a fluorine-containing ethylenic monomer and
represented by the formula (M4): 99wherein X.sup.1 and X.sup.2 are
the same or different and each is H or F; X.sup.3 is H, F, CH.sub.3
or CF.sub.3; X.sup.4 and X.sup.5 are the same or different and each
is H, F or CF.sub.3; Rf.sup.2 is an organic group in which 1 to 3
of Y.sup.6 having 3 to 10 carbon atoms and represented by the
formula: R.sup.2.paren close-st..sub.gO(C.dbd.O.paren
close-st.R.sup.1.paren close-st..sub.fCX.sup.6.dbd.CX.sup.7X.sup.8
wherein R.sup.1, X.sup.6, X.sup.7, X.sup.8 and f are as defined
above; R.sup.2 is a divalent organic group which has 1 to 7 carbon
atoms and may be substituted with fluorine atom; g is 0 or 1, are
bonded to a fluorine-containing alkyl group having 1 to 40 carbon
atoms or a fluorine-containing alkyl group having 2 to 100 carbon
atoms and ether bond; a is 0 or an integer of from 1 to 3; b and c
are the same or different and each is 0 or 1, the structural unit A
is a structural unit derived from monomer copolymerizable with the
fluorine-containing ethylenic monomer represented by the formula
(M4), and the structural unit M4 and the structural unit A are
contained in amounts of from 0.1 to 100% by mole and from 0 to
99.9% by mole, respectively.
16. A cured article which is obtained by photo-curing a curable
fluorine-containing resin composition comprising: (a) the curable
fluorine-containing polymer of any of claims 1 to 14, and (b) a
curing initiator which initiates curing with active energy.
17. A fluorine-containing resin composition for coating which
comprises: (a) the curable fluorine-containing polymer of any of
claims 1 to 14, (b) a curing initiator which initiates curing with
active energy, and (c) a solvent.
18. The fluorine-containing resin composition for coating of claim
17, wherein the solvent (c) is at least one selected from the group
consisting of ketone solvents, acetic acid ester solvents, alcohol
solvents and aromatic hydrocarbon solvents.
19. A cured film which is obtained by photo-curing a coating film
formed by applying the fluorine-containing resin composition for
coating of claim 17 or 18.
20. An antireflection film which is a cured film of a
fluorine-containing prepolymer, wherein said fluorine-containing
prepolymer has: (i) a carbon-carbon unsaturated bond at an end of
its side chain, and (ii) a refractive index of not more than 1.40,
and a thickness of the cured film is from 0.03 to 0.5 .mu.m.
21. An antireflection film which is a cured film obtained by
photo-curing a coating film formed by coating a composition for
coating which comprises: (d) the prepolymer of claim 20, (e) a
curing initiator which initiates curing with active energy, and (f)
a solvent, in which a thickness of said cured film is from 0.03 to
0.5 .mu.m.
22. An antireflection film which is a cured film obtained by
photo-curing a coating film formed by coating a composition for
coating which comprises: (d) the prepolymer of claim 20, (e) a
curing initiator which initiates curing with active energy, (f) a
solvent, and (g) a curing agent in which a thickness of said cured
film is from 0.03 to 0.5 .mu.m.
23. The antireflection film of claim 21 or 22, wherein the solvent
(f) is at least one selected from the group consisting of ketone
solvents, acetic acid ester solvents, alcohol solvents and aromatic
hydrocarbon solvents.
24. The antireflection film of any of claims 20 to 23, wherein the
carbon-carbon unsaturated bond at an end of the fluorine-containing
prepolymer is an ethylenic carbon-carbon double bond.
25. The antireflection film of claim 24, wherein the carbon-carbon
unsaturated bond at an end of the fluorine-containing prepolymer is
a radically polymerizable carbon-carbon double bond.
26. The antireflection film of any of claims 20 to 23, wherein the
fluorine-containing prepolymer is at least one of the curable
fluorine-containing polymers of claims 1 to 14.
27. The antireflection film of any of claims 22 to 26, wherein the
curing agent (g) is at least one selected from polyfunctional
acrylates obtained by replacing, with acrylate groups, two or more
hydroxyl groups of polyalcohols having a fluorine-containing alkyl
group which may have an ether bond or a fluorine-containing
alkylene group which may have an ether bond; polyfunctional
methacrylates obtained by replacing, with methacrylate groups, two
or more hydroxyl groups of polyalcohols having a
fluorine-containing alkyl group which may have an ether bond or a
fluorine-containing alkylene group which may have an ether bond;
and polyfunctional .alpha.-fluoroacrylates obtained by replacing,
with .alpha.-fluoroacrylate groups, two or more hydroxyl groups of
polyalcohols having a fluorine-containing alkyl group which may
have an ether bond or a fluorine-containing alkylene group which
may have an ether bond.
28. The antireflection film of claim 27, wherein the curing agent
(g) is at least one of polyfunctional .alpha.-fluoroacrylates.
29. The antireflection film of any of claims 20 to 28, wherein a
refractive index of the cured film is not more than 1.45.
30. An antireflection-treated article obtained by forming the
antireflection film of any of claims 20 to 29 on a substrate.
31. The antireflection-treated article of claim 30, wherein a
material of the substrate is at least one selected from the group
consisting of an acrylic resin, polycarbonate, polyethylene
terephthalate, polyolefin and triacetyl cellulose.
32. A fluorine-containing unsaturated compound represented by the
formula (4-1):
CX.sup.1X.sup.2.dbd.CX.sup.3--(CX.sup.4X.sup.5).sub.a--(O).sub.c---
Rf' (4-1) wherein X.sup.1 and X.sup.2 are the same or different and
each is H or F; X.sup.3 is H, F, CH.sub.3 or CF.sub.3; X.sup.4 and
X.sup.5 are the same or different and each is H, F or CF.sub.3; Rf'
is an organic group in which 1 to 3 of Y.sup.3 (Y.sup.3 is a
monovalent organic group having 2 to 10 carbon atoms and an
ethylenic carbon-carbon double bond at its end) are bonded to a
fluorine-containing alkyl group having 1 to 40 carbon atoms or a
fluorine-containing alkyl group having 2 to 100 carbon atoms and
ether bond; a is 0 or an integer of from 1 to 3; c is 0 or 1, said
Y.sup.3 is an organic group represented by the formula:
--(O).sub.d--(C.dbd.O)--Y.sup.4 wherein Y.sup.4 is an alkenyl group
or fluorine-containing alkenyl group having 2 to 5 carbon atoms and
an ethylenic carbon-carbon double bond at its end, d is 0 or 1.
33. The fluorine-containing unsaturated compound of claim 32 which
is represented by the formula (4-3):
CH.sub.2.dbd.CF--CF.sub.2--O--Rf' (4-3) wherein Rf' is as defined
in the formula (4-1).
34. The fluorine-containing unsaturated compound of claim 32 or 33,
wherein Y.sup.4 is represented by the formula:
--O(C.dbd.O)CX.sup.6.dbd.C- X.sup.7X.sup.8 wherein X.sup.6 is H, F,
CH.sub.3 or CF.sub.3; X.sup.7 and X.sup.8 are the same or different
and each is H or F.
Description
TECHNICAL FIELD
[0001] The present invention relates to a novel curable
fluorine-containing polymer, a curable resin composition prepared
from same and a cured article and cured film obtained by curing the
curable fluorine-containing polymer and also relates to an
antireflection film obtained from the cured film and an
antireflection-treated article provided with the antireflection
film.
BACKGROUND ART
[0002] As a result of development of multi-media, it has become
more important to secure an increased visible area (a property of
decreasing surface-reflected area when viewing at an angle, which
is also called "visibility") of a display of various displaying
devices. A large size displaying device is also required to have
well visible display, which is a problem to be solved from
technical point of view.
[0003] In order to enhance visibility of the displaying device, an
antireflection film made of a material having a low refractive
index has been formed on a substrate of the displaying device. For
forming an antireflection film, there is known, for example, a
method of forming a thin film of a fluorine-containing compound by
a deposition method. However in the deposition method, it is
difficult to form a coating film on a substrate for a large display
and yet a cost is high since a vacuum equipment is required.
[0004] Such being the case, there have been studied methods of
forming an antireflection film by preparing a liquid composition by
dissolving a fluorine-containing polymer having a low refractive
index in an organic solvent and then coating the obtained
composition on a surface of a substrate (for example, JP6-115023A,
etc.).
[0005] However in the method of coating the fluorine-containing
polymer solution, hardness of a coating film is insufficient and
therefore the coating film is damaged and peeled off due to
abrasion, thereby lowering appearance of a display.
[0006] Therefore there have been studied methods of preparing a
composition by mixing a photo-curable acrylic monomer, for example,
a fluorine-containing acrylic monomer or a fluorine-containing
polyfunctional acrylic compound to a fluorine-containing polymer
having a low refractive index and after coating the composition,
photo-curing the acrylic monomer (JP7-126552A, JP7-188588A,
JP8-48935A, etc.).
[0007] However in those methods, hardness of the coating film is
still insufficient because the fluorine-containing polymer itself
which is the main component is not crosslinked. In order to
increase the hardness, an amount of the acrylic monomer or the
polyfunctional acrylic compound may be increased, but in that case,
a refractive index of the cured film is increased and an intended
reflection reducing effect is lowered. Also in those methods, the
un-reacted acrylic monomer or polyfunctional acrylic compound is
apt to remain in the coating film, which causes lowering of
physical properties of the cured coating film.
[0008] Also methods of mixing a fluorine-containing polymer having
a photo-reactive (photo-polymerizable) functional group introduced
in its side chain with an acrylic monomer or polyfunctional acrylic
compound and photo-curing after coating the mixture have been
studied (JP 2527186 and JP 2543903). However the
fluorine-containing polymers described therein are high in a
refractive index and therefore are insufficient in performance for
an antireflection film. In addition, as the number of cure sites of
the fluorine-containing polymer is increased to increase hardness,
a refractive index becomes high and therefore a reflection reducing
effect is further lowered.
[0009] An object of the present invention is to provide a curable
fluorine-containing polymer which can make its hardness high by
photo-curing while maintaining a low refractive index.
[0010] Another object of the present invention is to provide an
antireflection film possessing improved scratch resistance and
abrasion resistance while maintaining a reflection reducing effect
and also to provide an antireflection-treated article having such
an antireflection film thereon.
DISCLOSURE OF INVENTION
[0011] The present inventors have made intensive studies to achieve
those objects and have found novel curable fluorine-containing
polymers having an ethylenic carbon-carbon double bond in its side
chain and have found that when those polymers are used, a cured
article having a high hardness can be obtained while maintaining a
low refractive index.
[0012] Further the present inventors have found that a cured film
of a specific fluorine-containing polymer having a carbon-carbon
unsaturated bond at an end of its side chain is useful as an
antireflection film having both of low reflection and high
hardness.
[0013] The present inventors have completed the present invention
mentioned below based on the above-mentioned findings.
[0014] The first of the present invention relates to a curable
fluorine-containing polymer having an ethylenic carbon-carbon
double bond in its side chain.
[0015] The curable fluorine-containing polymer of the present
invention has a number average molecular weight of from 500 to
1,000,000 and is represented by the formula (1): M.paren
close-st.A.paren close-st. (1)
[0016] in which the structural unit M is a structural unit derived
from fluorine-containing ethylenic monomer and represented by the
formula (M): 2
[0017] wherein X.sup.1 and X.sup.2 are the same or different and
each is H or F; X.sup.3 is H, F, CH.sub.3 or CF.sub.3; X.sup.4 and
X.sup.5 are the same or different and each is H, F or CF.sub.3; Rf
is an organic group in which 1 to 3 of Y.sup.1 (Y.sup.1 is a
monovalent organic group having 2 to 10 carbon atoms and an
ethylenic carbon-carbon double bond at its end) are bonded to a
fluorine-containing alkyl group having 1 to 40 carbon atoms or a
fluorine-containing alkyl group having 2 to 100 carbon atoms and
ether bond; a is 0 or an integer of from 1 to 3; b and c are the
same or different and each is 0 or 1,
[0018] the structural unit A is a structural unit derived from
monomer copolymerizable with the fluorine-containing ethylenic
monomer represented by the formula (M),
[0019] and the structural unit M and the structural unit A are
contained in amounts of from 0.1 to 100% by mole and from 0 to
99.9% by mole, respectively.
[0020] The second of the present invention relates to a process for
preparing a curable fluorine-containing polymer having a number
average molecular weight of from 500 to 1,000,000 which is
characterized by esterifying:
[0021] fluorine-containing polymer having hydroxyl and represented
by the formula (2)
N.paren close-st.B.paren close-st. (2)
[0022] in which the structural unit N is a structural unit having
hydroxyl and derived from fluorine-containing ethylenic monomer and
is represented by the formula (N): 3
[0023] wherein X.sup.1 and X.sup.2 are the same or different and
each is H or F; X.sup.3 is H, F, CH.sub.3 or CF.sub.3; X.sup.4 and
X.sup.5 are the same or different and each is H, F or CF.sub.3;
Rf.sup.1 is an organic group in which 1 to 3 of Y.sup.5 (Y.sup.5 is
hydroxyl or a monovalent organic group having 1 to 10 carbon atoms
and hydroxyl) are bonded to a fluorine-containing alkyl group
having 1 to 40 carbon atoms or a fluorine-containing alkyl group
having 2 to 100 carbon atoms and ether bond; a is 0 or an integer
of from 1 to 3; b and c are the same or different and each is 0 or
1,
[0024] the structural unit (B) is a structural unit derived from
monomer copolymerizable with the fluorine-containing ethylenic
monomer having hydroxyl which is represented by the above-mentioned
formula (N), and the structural unit N and the structural unit B
are contained in amounts of from 0.1 to 100% by mole and from 0 to
99.9% by mole, respectively, with an unsaturated carboxylic acid or
its derivative having 3 to 10 carbon atoms (a total number of
carbon atoms including carbon atoms of Y.sup.3 is from 3 to 10) and
represented by the formula:
HOOCR.sup.1.paren close-st..sub.fCX.sup.6.dbd.CX.sup.7X.sup.8
[0025] wherein R.sup.1 is a divalent organic group which has 1 to 7
carbon atoms and may be substituted with fluorine atom; X.sup.6 is
H, F, CH.sub.3 or CF.sub.3; X.sup.7 and X.sup.8 are the same or
different and each is H or F; f is 0 or 1. The obtained curable
fluorine-containing polymer is represented by the formula (1a):
M4.paren close-st.A.paren close-st. (1a)
[0026] in which the structural unit M4 is a structural unit derived
from a fluorine-containing ethylenic monomer and represented by the
formula (M4): 4
[0027] wherein X.sup.1 and X.sup.2 are the same or different and
each is H or F; X.sup.3 is H, F, CH.sub.3 or CF.sub.3; X.sup.4 and
X.sup.5 are the same or different and each is H, F or CF.sub.3;
Rf.sup.2 is an organic group in which 1 to 3 of Y.sup.6 having 3 to
10 carbon atoms and represented by the formula:
R.sup.2.paren close-st..sub.gO(C.dbd.O.paren close-st.R.sup.1.paren
close-st..sub.fCX.sup.6.dbd.CX.sup.7X.sup.8
[0028] wherein R.sup.1, X.sup.6, X.sup.7, X.sup.8 and f are as
defined above; R.sup.2 is a divalent organic group which has 1 to 7
carbon atoms and may be substituted with fluorine atom; g is 0 or
1, are bonded to a fluorine-containing alkyl group having 1 to 40
carbon atoms or a fluorine-containing alkyl group having 2 to 100
carbon atoms and ether bond; a is 0 or an integer of from 1 to 3; b
and c are the same or different and each is 0 or 1,
[0029] the structural unit A is a structural unit derived from
monomer copolymerizable with the fluorine-containing ethylenic
monomer represented by the formula (M4), and
[0030] the structural unit M4 and the structural unit A are
contained in amounts of from 0.1 to 100% by mole and from 0 to
99.9% by mole, respectively.
[0031] The third of the present invention relates to a
fluorine-containing resin composition for coating which
comprises:
[0032] (a) the above-mentioned curable fluorine-containing polymer
or any of the curable fluorine-containing polymers of claims 2 to
14,
[0033] (b) an active energy curing initiator which initiates curing
with active energy, and
[0034] (c) a solvent, if necessary,
[0035] and relates to a cured article obtained therefrom,
particularly a photo-cured article and a cured film.
[0036] The fourth of the present invention relates to an
antireflection film.
[0037] The antireflection film is
[0038] an antireflection film which is a cured film of a
fluorine-containing prepolymer, in which the fluorine-containing
prepolymer has:
[0039] (i) a carbon-carbon unsaturated bond at an end of its side
chain, and
[0040] (ii) a refractive index of not more than 1.40,
[0041] and a thickness of the cured film is from 0.03 to 0.5
.mu.m;
[0042] an antireflection film which is a cured film obtained by
photo-curing a coating film formed by coating a composition for
coating which comprises:
[0043] (d) the above-mentioned fluorine-containing prepolymer,
[0044] (e) an active energy curing initiator which initiates curing
with active energy, and
[0045] (f) a solvent,
[0046] in which a thickness of the cured film is from 0.03 to 0.5
.mu.m; or an antireflection film which is a cured film obtained by
photo-curing a coating film formed by coating a composition for
coating which comprises:
[0047] (d) the above-mentioned fluorine-containing prepolymer,
[0048] (e) an active energy curing initiator which initiates curing
with active energy,
[0049] (f) a solvent, and
[0050] (g) a curing agent,
[0051] in which a thickness of the cured film is from 0.03 to 0.5
.mu.m.
[0052] The fifth of the present invention relates to an
antireflection-treated article obtained by applying the
above-mentioned antireflection film on a substrate.
[0053] The sixth of the present invention relates to a novel
fluorine-containing unsaturated compound. The novel compound is a
fluorine-containing unsaturated compound represented by the formula
(4-1):
CX.sup.1X.sup.2.dbd.CX.sup.3--(CX.sup.4X.sup.5).sub.a--(O).sub.c--Rf'
(4-1)
[0054] wherein X.sup.1 and X.sup.2 are the same or different and
each is H or F; X.sup.3 is H, F, CH.sub.3 or CF.sub.3; X.sup.4 and
X.sup.5 are the same or different and each is H, F or CF.sub.3; Rf'
is an organic group in which 1 to of 3 Y.sup.3 (Y.sup.3 is a
monovalent organic group having 2 to 10 carbon atoms and an
ethylenic carbon-carbon double bond at its end) are bonded to a
fluorine-containing alkyl group having 1 to 40 carbon atoms or a
fluorine-containing alkyl group having 2 to 100 carbon atoms and
ether bond; a is 0 or an integer of from 1 to 3; c is 0 or 1,
[0055] in which Y.sup.3 is an organic group represented by the
formula:
--(O).sub.d--(C.dbd.O)--Y.sup.4
[0056] wherein Y.sup.4 is an alkenyl group or fluorine-containing
alkenyl group having 2 to 5 carbon atoms and an ethylenic
carbon-carbon double bond at its end and d is 0 or 1.
BEST MODE FOR CARRYING OUT THE INVENTION
[0057] The curable fluorine-containing polymer of the first
invention is, as mentioned above, the curable fluorine-containing
polymer which has a number average molecular weight of from 500 to
1,000,000 and is represented by the formula (1):
M.paren close-st.A.paren close-st. (1)
[0058] in which the structural unit M is a structural unit
represented by the formula (M): 5
[0059] wherein X.sup.1 and X.sup.2 are the same or different and
each is H or F; X.sup.3 is H, F, CH.sub.3 or CF.sub.3; X.sup.4 and
X.sup.5 are the same or different and each is H, F or CF.sub.3; Rf
is an organic group in which 1 to 3 of Y.sup.1 (Y.sup.1 is a
monovalent organic group having 2 to 10 carbon atoms and an
ethylenic carbon-carbon double bond at its end) are bonded to a
fluorine-containing alkyl group having 1 to 40 carbon atoms or a
fluorine-containing alkyl group having 2 to 100 carbon atoms and
ether bond; a is 0 or an integer of from 1 to 3; b and c are the
same or different and each is 0 or 1,
[0060] the structural unit A is a structural unit derived from
monomer copolymerizable with the fluorine-containing ethylenic
monomer represented by the formula (M), and
[0061] the structural unit M and the structural unit A are
contained in amounts of from 0.1 to 100% by mole and from 0 to
99.9% by mole, respectively.
[0062] The structural unit M is a structural unit derived from a
fluorine-containing ethylenic monomer represented by the formula
(3):
CX.sup.1X.sup.2.dbd.CX.sup.3--(CX.sup.4X.sup.5).sub.a--(C.dbd.O).sub.b--(O-
).sub.c--Rf (3)
[0063] wherein X.sup.1, X.sup.2, X.sup.3, X.sup.4, X.sup.5, Rf, a,
b and c are as defined in the formula (M).
[0064] Namely, the curable fluorine-containing polymer is a
homopolymer of the above-mentioned fluorine-containing ethylenic
monomer having, in its side chain, an ethylenic carbon-carbon
double bond curable by a reaction or a copolymer having the
fluorine-containing ethylenic monomer as an essential
component.
[0065] It is preferable that at least one of Y.sup.1 is bonded to
an end of Rf.
[0066] In the curable fluorine-containing polymer of the formula
(1) of the present invention, the structural unit M is preferably a
structural unit M1 represented by: 6
[0067] wherein X.sup.1 and X.sup.2 are the same or different and
each is H or F; X.sup.3 is H, F, CH.sub.3 or CF.sub.3; X.sup.4 and
X.sup.5 are the same or different and each is H, F or CF.sub.3; Rf
is an organic group in which 1 to 3 of Y.sup.1 (Y.sup.1 is a
monovalent organic group having 2 to 10 carbon atoms and an
ethylenic carbon-carbon double bond at its end) are bonded to a
fluorine-containing alkyl group having 1 to 40 carbon atoms or a
fluorine-containing alkyl group having 2 to 100 carbon atoms and
ether bond; a is 0 or an integer of from 1 to 3; c is 0 or 1.
[0068] The structural unit M1 is a structural unit derived from a
fluorine-containing ethylenic monomer represented by:
CX.sup.1X.sup.2.dbd.CX.sup.3--(CX.sup.4X.sup.5).sub.a--(O).sub.c--Rf
(4)
[0069] wherein X.sup.1, X.sup.2, X.sup.3, X.sup.4, X.sup.5, Rf, a
and c are as defined in the formula (3). Among the
fluorine-containing unsaturated compounds represented by the
formula (4), the fluorine-containing unsaturated compound
represented by the formula (4-1):
CX.sup.1X.sup.2.dbd.CX.sup.3--(CX.sup.4X.sup.5).sub.a--(O)--Rf'
(4-1)
[0070] wherein X.sup.1, X.sup.2, X.sup.3, X.sup.4, X.sup.5, a and c
are as defined in the formula (4); Rf' is an organic group in which
1 to 3 of Y.sup.3 (Y.sup.3 is a monovalent organic group having 2
to 10 carbon atoms and an ethylenic carbon-carbon double bond at
its end) are bonded to a fluorine-containing alkyl group having 1
to 40 carbon atoms or a fluorine-containing alkyl group having 2 to
100 carbon atoms and ether bond,
[0071] in which Y.sup.3 is an organic group represented by the
formula:
--(O).sub.d--(C.dbd.O)--Y.sup.4
[0072] wherein Y.sup.4 is an alkenyl group or fluorine-containing
alkenyl group having 2 to 5 carbon atoms and an ethylenic
carbon-carbon double bond at its end, d is 0 or 1,
[0073] is a novel compound which has not been disclosed in any
publications.
[0074] The polymer containing the above-mentioned structural unit
M1 is particularly low in refractive index, and is preferred
particularly since a refractive index can be decreased even in the
cases of a M1 homopolymer and a polymer containing the M1 in an
increased amount.
[0075] More preferable example of M1 is a structural unit M2
represented by: 7
[0076] wherein Rf is an organic group in which 1 to 3 of Y.sup.1
(Y.sup.1 is a monovalent organic group having 2 to 10 carbon atoms
and an ethylenic carbon-carbon double bond at its end) are bonded
to a fluorine-containing alkyl group having 1 to 40 carbon atoms or
a fluorine-containing alkyl group having 2 to 100 carbon atoms and
ether bond.
[0077] The structural unit M2 is a structural unit derived from a
fluorine-containing ethylenic monomer represented by the formula
(4-2):
CH.sub.2.dbd.CF--CF.sub.2--O--Rf (4-2)
[0078] wherein Rf is as defined in the formula (3). Among the
fluorine-containing unsaturated compounds represented by the
formula (4-2), a fluorine-containing unsaturated compound
represented by the formula (4-3):
CH.sub.2.dbd.CFCF.sub.2ORf' (4-3)
[0079] wherein Rf' is as defined in the formula (4-1), is a novel
compound which has not been disclosed in any publications.
[0080] Namely, the above-mentioned M2 is a structural unit of a
fluorine-containing allyl ether having an ethylenic carbon-carbon
double bond at its end and is preferred since not only a refractive
index can be decreased but also polymerizability thereof,
particularly homo-polymerizability and copolymerizability with the
fluorine-containing ethylenic monomer are good.
[0081] Another example of preferable M1 is a structural unit M3
represented by: 8
[0082] wherein Rf is an organic group in which 1 to 3 of Y.sup.1
(Y.sup.1 is a monovalent organic group having 2 to 10 carbon atoms
and an ethylenic carbon-carbon double bond at its end) are bonded
to a fluorine-containing alkyl group having 1 to 40 carbon atoms or
a fluorine-containing alkyl group having 2 to 100 carbon atoms and
ether bond.
[0083] The structural unit M3 is a structural unit derived from a
fluorine-containing ethylenic monomer represented by the formula
(4-4):
CF.sub.2.dbd.CF--O--Rf (4-4)
[0084] wherein Rf is as defined in the formula (3). Among the
fluorine-containing unsaturated compounds represented by the
formula (4-4), the fluorine-containing unsaturated compound
represented by the formula (4-5):
CF.sub.2.dbd.CFORf' (4-5)
[0085] wherein Rf' is as defined in the formula (4-1) is a novel
compound which has not been disclosed in any publications.
[0086] The above-mentioned M3 is a structural unit of a
fluorine-containing vinyl ether having an ethylenic carbon-carbon
double bond at its end and is preferred since a refractive index
can be decreased and copolymerizability with the
fluorine-containing ethylenic monomer is good.
[0087] In the curable fluorine-containing polymer of the formula
(1) of the present invention, Y.sup.1 contained in the structural
units M, M1, M2 and M3 is an organic group having 2 to 10 carbon
atoms and an ethylenic carbon-carbon double bond at its end.
[0088] Namely, the carbon-carbon double bond in Y.sup.1 has an
ability of causing polycondensation reaction, ring formation
reaction and addition reaction, and thereby a cured (crosslinked)
article can be obtained. Concretely, for example, by contact of the
carbon-carbon double bond with radical or cation, there arise a
polymerization reaction and condensation reaction between molecules
of the curable fluorine-containing polymer of the present invention
or between the curable fluorine-containing polymer and the curing
(crosslinking) agent added as case demands, and thus a cured
(crosslinked) article can be obtained.
[0089] In the curable fluorine-containing polymers of the formulae
(1) and (2) of the present invention, preferable Y.sup.1 is:
O.paren close-st..sub.dC.dbd.O.paren close-st..sub.eY.sup.2
[0090] wherein Y.sup.2 is an alkenyl group or fluorine-containing
alkenyl group having 2 to 5 carbon atoms and an ethylenic
carbon-carbon double bond at its end, d and e are the same or
different and each is 0 or 1, and preferable Y.sup.2 is:
--CX.sup.6.dbd.CX.sup.7X.sup.8
[0091] wherein X.sup.6 is H, F, CH.sub.3 or CF.sub.3; X.sup.7 and
X.sup.8 are H or F since curing reactivity thereof by contact with
radical or cation is high.
[0092] Examples of the preferable Y.sup.4 in the novel
fluorine-containing unsaturated compounds of the present invention
represented by (4-1), (4-3) and (4-5) are the same as the
above-mentioned Y.sup.2.
[0093] Examples of the preferable Y.sup.2 and Y.sup.4 are: 9
[0094] Examples of more preferable Y.sup.1 and Y.sup.3 are:
--O(C.dbd.O)CX.sup.6.dbd.CX.sup.7X.sup.8
[0095] wherein X.sup.6 is H, F, CH.sub.3 or CF.sub.3, X.sup.7 and
X.sup.8 are H or F, which are preferred since a curing reactivity
by contact with radical is particularly higher and a cured article
can be obtained easily by photo-curing, etc.
[0096] Examples of the above-mentioned Y.sup.1 and Y.sup.3 are:
10
[0097] and the like.
[0098] Other examples of Y.sup.1 are: 11
[0099] and the like.
[0100] Other examples of Y.sup.3 are: 12
[0101] and the like.
[0102] Particularly those which have a structure of
--O(C.dbd.O)CF.dbd.CH.sub.2 are preferred since a refractive index
can be reduced and a curing (crosslinking) reactivity is
particularly high, which enables a cured article to be obtained
effectively.
[0103] In Rf contained in the structural units M, M1, M2 and M3 of
the curable fluorine-containing polymer of the formula (1) of the
present invention, Rf' contained in the novel fluorine-containing
unsaturated compounds represented by the formulae (4-1), (4-3) and
(4-5), Rf.sup.1 contained in the structural unit N of the
fluorine-containing polymer of the formula (2) having hydroxyl and
further Rf.sup.4 and Rf.sup.6 contained in the structural units
(A1) and (A2) of the curable fluorine-containing polymer of the
formula (1-1), examples of preferable organic groups excluding the
functional groups Y.sup.1, Y.sup.3, Y.sup.5, Z.sup.1 and Z.sup.2
are fluorine-containing alkylene groups having 1 to 40 carbon atoms
and fluorine-containing alkylene groups having 2 to 100 carbon
atoms and ether bond particularly in case where the number of
functional groups Y.sup.1, Y.sup.3 or Y.sup.5 is one. In those
organic groups, fluorine atom is bonded to carbon atom contained
therein. Generally those organic groups are fluorine-containing
alkylene groups or fluorine-containing alkylene groups having ether
bond, in which fluorine atom and hydrogen atom or chlorine atom are
bonded to carbon atom. Preferred are those having more fluorine
atoms (a higher fluorine content). The fluorine content is not less
than 50%, preferably not less than 70% on the basis of a molecular
weight of the organic groups provided that oxygen atoms in the
organic groups and the functional groups are eliminated from
calculation. More preferred are perfluoro alkylene groups or
perfluoro alkylene groups having ether bond. Those organic groups
are preferred since a refractive index of the curable
fluorine-containing polymer can be reduced, particularly since a
low refractive index can be maintained even when a curing degree
(density of crosslinking) is made high to increase hardness of the
cured article.
[0104] Too large number of carbon atoms is not preferable because
in case of the fluorine-containing alkylene groups, there is a case
where solubility in a solvent is lowered and transparency is
lowered and in case of the fluorine-containing alkylene groups
having ether bond, there is a case where hardness and mechanical
properties of the polymer itself and the cured article obtained
therefrom are lowered. The number of carbon atoms of the
fluorine-containing alkylene groups is preferably from 1 to 20,
more preferably from 1 to 10, and the number of carbon atoms of the
fluorine-containing alkylene groups having ether bond is preferably
from 2 to 30, more preferably from 2 to 20
[0105] Preferable example thereof is: 13
[0106] (1: from 1 to 10, m: from 1 to 10, n: from 0 to 5) 14
[0107] (X.sup.9 and X.sup.9' are F or CF.sub.3; X.sup.10 and
X.sup.10' are H or F; o+p+q is from 1 to 30; r is 0 or 1; s and t
are 0 or 1).
[0108] Mentioned below are structures of the structural unit M
constituting the curable fluorine-containing polymer of the present
invention and examples of the novel fluorine-containing unsaturated
compound.
[0109] Examples of the preferable monomer giving the structural
unit M2 are: 15
[0110] (n: an integer of from 1 to 30)
[0111] CH.sub.2.dbd.CFCF.sub.2OCF.sub.2CF.sub.2O.paren
close-st..sub.nCF.sub.2--Y.sup.1,
[0112] CH.sub.2.dbd.CFCF.sub.2OCF.sub.2CF.sub.2O.paren
close-st..sub.nCF.sub.2CH.sub.2--Y.sub.1,
[0113] CH.sub.2.dbd.CFCF.sub.2OCF.sub.2CF.sub.2CF.sub.2O.paren
close-st..sub.nCF.sub.2CF.sub.2--Y.sup.1,
[0114] CH.sub.2.dbd.CFCF.sub.2OCF.sub.2CF.sub.2CF.sub.2O.paren
close-st..sub.nCF.sub.2CF.sub.2CH.sub.2--Y.sup.1,
[0115] CH.sub.2.dbd.CFCF.sub.2OCH.sub.2CF.sub.2CF.sub.2O.paren
close-st..sub.nCH.sub.2CF.sub.2--Y.sub.1,
[0116] CH.sub.2.dbd.CFCF.sub.2OCH.sub.2CF.sub.2CF.sub.2O.paren
close-st..sub.nCH.sub.2CF.sub.2CH.sub.2--Y.sup.1,
[0117] (n: an integer of from 1 to 30) 16
[0118] and the like. More concretely there are: 17
[0119] (X is H, CH.sub.3, F or CF.sub.3; n is 0 or an integer of
from 1 to 30) 18
[0120] (n is 0 or an integer of from 1 to 30) 19
[0121] (Rf.sup.1 and Rf.sup.2 are perfluoroalkyl groups having 1 to
5 carbon atoms; n is 0 or an integer of from 1 to 30) 20
[0122] (X is H, CH.sub.3, F or CF.sub.3; n is 0 or an integer of
from 1 to 30)
[0123] and the like.
[0124] Preferable examples of the novel fluorine-containing
unsaturated compound of the formula (4-3) are those exemplified
above as the monomer giving the structural unit M2, in which
Y.sup.1 is replaced with Y.sup.3.
[0125] More concretely there are: 21
[0126] (X is H, CH.sub.3, F or CF.sub.3; n is 0 or an integer of
from 1 to 30) 22
[0127] (Rf.sup.1 and Rf.sup.2 are perfluoroalkyl groups having 1 to
5 carbon atoms; n is 0 or an integer of from 1 to 30) 23
[0128] (X is H, CH.sub.3, F or CF.sub.3; n is 0 or an integer of
from 1 to 30)
[0129] and the like.
[0130] Examples of the preferable monomer giving the structural
unit M3 are:
[0131] CF.sub.2.dbd.CFOCF.sub.2CF.sub.2--Y.sup.1,
CF.sub.2.dbd.CFOCF.sub.2- CF.sub.2CH.sub.2--Y.sup.1, 24
[0132] (n is from 1 to 30)
[0133] CF.sub.2.dbd.CFOCF.sub.2.paren close-st..sub.3Y.sup.1,
CF.sub.2.dbd.CFOCF.sub.2.paren
close-st..sub.3CH.sub.2--Y.sup.1,
[0134] CF.sub.2.dbd.CFOCF.sub.2CF.sub.2OCF.sub.2--Y.sup.1,
[0135] CF.sub.2.dbd.CFOCF.sub.2CF.sub.2OCF.sub.2CH.sub.2--Y.sup.1,
25
[0136]
CF.sub.2.dbd.CFOCF.sub.2CF.sub.2CH.sub.2OCF.sub.2CF.sub.2--Y.sup.1,
[0137]
CF.sub.2.dbd.CFOCF.sub.2CF.sub.2CH.sub.2OCF.sub.2CF.sub.2CH.sub.2---
Y.sup.1
[0138] and the like.
[0139] More concretely there are: 26
[0140] (Rf.sup.1 and Rf.sup.2 are perfluoroalkyl groups having 1 to
5 carbon atoms) 27
[0141] (m is from 0 to 30, n is from 1 to 3, X is H, CH.sub.3, F or
CF.sub.3)
[0142] and the like.
[0143] Preferable examples of the novel fluorine-containing
unsaturated compound of the formula (4-5) are those exemplified
above as the monomer giving the structural unit M3, in which
Y.sup.1 is replaced with Y.sup.3.
[0144] More concretely there are: 28
[0145] (Rf.sup.1 and Rf.sup.2 are perfluoroalkyl groups having 1 to
5 carbon atoms) 29
[0146] (m is from 0 to 30, n is from 1 to 3, X is H, CH.sub.3, F or
CF.sub.3)
[0147] and the like.
[0148] Examples of a preferable monomer constituting the structural
unit M of the curable fluorine-containing polymer of the present
invention other than M2 and M3 are, for instance, 30
[0149] and the like, wherein Rf is as defined above.
[0150] More concretely there are:
[0151] CF.sub.2.dbd.CFCF.sub.2OCF.sub.2CF.sub.2CF.sub.2--Y.sup.1,
CF.sub.2.dbd.CFCF.sub.2OCF.sub.2CF.sub.2CF.sub.2CH.sub.2--Y.sup.1,
31
[0152] CF.sub.2.dbd.CFCF.sub.2--Y.sup.1,
CF.sub.2.dbd.CFCF.sub.2CH.sub.2--- Y.sup.1, 32
[0153] CH.sub.2.dbd.CHCF.sub.2CF.sub.2CH.sub.2CH.sub.2--Y.sup.1,
CH.sub.2.dbd.CHCF.sub.2CF.sub.2--Y.sup.1,
[0154] CH.sub.2.dbd.CHCF.sub.2CF.sub.2CH.sub.2--Y.sup.1,
CH.sub.2.dbd.CHCF.sub.2CF.sub.2CF.sub.2CF.sub.2--Y.sup.1,
[0155]
CH.sub.2.dbd.CHCF.sub.2CF.sub.2CF.sub.2CF.sub.2CH.sub.2--Y.sup.1,
33
[0156] CH.sub.2.dbd.CHOCH.sub.2CF.sub.2CF.sub.2--Y.sup.1,
CH.sub.2.dbd.CHOCH.sub.2CF.sub.2CF.sub.2CH.sub.2--Y.sup.1
[0157] and the like.
[0158] In the novel fluorine-containing unsaturated compounds of
the formula (4-1) of the present invention, preferred examples of
the fluorine-containing unsaturated compounds other than those of
the above-mentioned formulae (4-3) and (4-5) are the monomers
exemplified above as the monomers giving the structural unit M
other than the structural units M2 and M3, in which Y.sup.1 is
replaced by Y.sup.3.
[0159] In the curable fluorine-containing polymer of the present
invention, the structural unit A is an optional component and is
not limited particularly as far as it is a monomer copolymerizable
with the structural unit M, M1, M2 or M3. The structural unit A may
be selected optionally depending on intended applications and
required characteristics of the curable fluorine-containing polymer
and the cured article obtained therefrom.
[0160] Examples of the structural unit A are, for instance,
[0161] {circle over (1)} Structural units (A1) derived from
fluorine-containing ethylenic monomers having functional group
[0162] These structural units are preferred from the point that
adhesion to a substrate and solubility in a solvent, particularly a
general-purpose solvent are imparted to the curable
fluorine-containing polymer while maintaining a low refractive
index of the polymer and the cured article obtained therefrom and
in addition, characteristics such as crosslinkability other than
those influenced by Y are imparted to the polymer. The structural
unit of the fluorine-containing ethylenic monomers having
functional group is represented by the formula (A1): 34
[0163] wherein X.sup.11, X.sup.12 and X.sup.13 are H or F; X.sup.14
is H, F or CF.sub.3; h is 0, 1 or 2; i is 0 or 1; Rf.sup.4 is a
fluorine-containing alkylene group having 1 to 40 carbon atoms or a
fluorine-containing alkylene group having 2 to 100 carbon atoms and
ether bond; Z.sup.1 is selected from --OH, --CH.sub.2OH, --COOH,
carboxylic acid derivative, --SO.sub.3H, sulfonic acid derivative,
epoxy group and cyano group. Particularly preferred is the
structural unit represented by the formula (A1-1): 35
[0164] wherein Rf.sup.4 and Z.sup.1 are as defined in the formula
(A1).
[0165] Concretely preferred are structural units derived from
fluorine-containing ethylenic monomers such as: 36
[0166] CH.sub.2.dbd.CFCF.sub.2OCH.sub.2CF.sub.2-Z.sup.1, 37
[0167] CH.sub.2.dbd.CFCF.sub.2OCF.sub.2CF.sub.2OCF.sub.2-Z.sup.1
and
[0168] CH.sub.2.dbd.CFCF.sub.2OCF.sub.2CF.sub.2O.paren
close-st..sub.2CF.sub.2-Z.sup.1.
[0169] Also there are preferable structural units represented by
the formula (A1-2): 38
[0170] wherein Rf.sup.4 and Z.sup.1 are as defined in the formula
(A1).
[0171] Concretely preferred are structural units derived from
monomers such as: 39
[0172] CF.sub.2.dbd.CFOCF.sub.2.paren close-st..sub.3Z.sub.1,
CF.sub.2.dbd.CFOCF.sub.2.paren close-st..sub.3CH.sub.2-Z.sup.1,
[0173] CF.sub.2.dbd.CFOCF.sub.2CF.sub.2OCF.sub.2-Z.sup.1,
CF.sub.2.dbd.CFOCF.sub.2CF.sub.2OCF.sub.2CH.sub.2-Z.sup.1,
[0174]
CF.sub.9.dbd.CFOCF.sub.2CF.sub.2CH.sub.2OCF.sub.2CF.sub.2-Z.sub.1,
[0175]
CF.sub.2.dbd.CFOCF.sub.2CF.sub.2CH.sub.2OCF.sub.2CF.sub.2CH.sub.2-Z-
.sup.1.
[0176] Examples of other fluorine-containing ethylenic monomers
having functional group are:
[0177] CF.sub.2.dbd.CFCF.sub.2--O--Rf-Z.sup.1,
CF.sub.2.dbd.CF--Rf-Z.sup.1- ,
[0178] CH.sub.2.dbd.CH--Rf-Z.sup.1, CH.sub.2.dbd.CHO--Rf-Z.sup.1
and the like,
[0179] wherein Rf is the same as Rf of the formula (M).
[0180] Concretely there are:
[0181] CF.sub.2.dbd.CFCF.sub.2OCF.sub.2CF.sub.2CF.sub.2-Z.sup.1,
CF.sub.2.dbd.CFCF.sub.2OCF.sub.2CF2CF.sub.2CH.sub.2-Z.sup.1, 40
[0182] CF.sub.2.dbd.CFCF.sub.2-Z.sup.1,
CF.sub.2.dbd.CFCF.sub.2CH.sub.2-Z.- sup.1,
[0183] CH.sub.2.dbd.CHCF.sub.2CF.sub.2CH.sub.2CH.sub.2-Z.sup.1,
CH.sub.2.dbd.CHCF.sub.2CF.sub.2-Z.sup.1,
[0184] CH.sub.2.dbd.CHCF.sub.2CF.sub.2CH.sub.2-Z.sup.1,
CH.sub.2.dbd.CHCF.sub.2CF.sub.2CF.sub.2CF.sub.2-Z.sup.1,
[0185]
CH.sub.2.dbd.CHCF.sub.2CF.sub.2CF.sub.2CF.sub.2CH.sub.2-Z.sup.1,
CH.sub.2.dbd.CHO--CH.sub.2CF.sub.2CF.sub.2-Z.sup.1,
[0186]
CH.sub.2.dbd.CHOCH.sub.2CF.sub.2CF.sub.2CH.sub.2-Z.sup.1,
[0187] and the like.
[0188] {circle over (2)} Structural units (A2) derived from
fluorine-containing ethylenic monomers not having functional
group
[0189] These structural units are preferred from the point that a
refractive index of the curable fluorine-containing polymer or the
cured article obtained therefrom can be kept low and the refractive
index can be further reduced. Also those structural units are
preferred since mechanical properties, glass transition
temperature, etc. of the polymer can be adjusted by selecting
monomers, particularly since the glass transition temperature can
be increased by copolymerizing with the structural unit M.
[0190] Preferred structural units of the fluorine-containing
ethylenic monomers are those represented by the formula (A2):
41
[0191] wherein X.sup.15, X.sup.16 and X.sup.18 are H or F; X.sup.17
is H, F or CF.sub.3; h1, i1 and j are 0 or 1; Z.sup.2 is H, F or
Cl; Rf.sup.5 is a fluorine-containing alkylene group having 1 to 20
carbon atoms or a fluorine-containing alkylene group having 2 to
100 carbon atoms and ether bond.
[0192] Preferred examples thereof are structural units derived from
monomers such as:
[0193] CF.sub.2.dbd.CF.sub.2, CF.sub.2.dbd.CH.sub.2,
CF.sub.2.dbd.CFCl, CF.sub.2.dbd.CFCF.sub.3, 42
[0194] CH.sub.2.dbd.CFCF.sub.2.paren close-st..sub.nZ.sup.2
(Z.sup.2 is as defined in the formula (A2), n: from 1 to 10),
CH.sub.2.dbd.CHOCH.sub.2CF- .sub.2.paren close-st..sub.nZ.sup.2
(Z.sup.2 is as defined in the formula (A2), n: from 1 to 10).
[0195] {circle over (3)} Fluorine-containing aliphatic ring
structural units (A3)
[0196] The introduction of these structural units is preferred
since transparency can be increased, a refractive index can be made
lower and further the curable fluorine-containing polymer having a
high glass transition temperature can be obtained and a higher
hardness of the cured article can be expected.
[0197] Preferred fluorine-containing aliphatic ring structural
units are those represented by the formula (A3): 43
[0198] wherein X.sup.19, X.sup.20, X.sup.23, X.sup.24, X.sup.25 and
X.sup.26 are the same or different and each is H or F; X.sup.21 and
X.sup.22 are the same or different and each is H, F, C.sub.1 or
CF.sub.3; Rf.sup.6 is a fluorine-containing alkylene group having 1
to 10 carbon atoms or a fluorine-containing alkylene group having 2
to 10 carbon atoms and ether bond; n2 is 0 or an integer of from 1
to 3; n1, n3, n4 and n5 are the same or different and each is 0 or
1.
[0199] For example, there are structural units represented by:
44
[0200] wherein Rf.sup.6, X.sup.21 and X.sup.22 are as defined
above.
[0201] Concretely there are: 45
[0202] and the like.
[0203] {circle over (4)} Structural units derived from ethylenic
monomers not having fluorine
[0204] The structural units derived from ethylenic monomers not
having fluorine may be introduced to the polymer in a range where
the introduction does not have an adverse effect on a refractive
index (in a range where the refractive index does not
increase).
[0205] The introduction of those structural units is preferred
since solubility in a general-purpose solvent is enhanced and
compatibility with additives, for example, a photocatalyst and a
curing agent to be added as case demands can be improved.
[0206] Examples of the non-fluorine-containing ethylenic monomer
are as follows.
[0207] .alpha.-Olefins:
[0208] Ethylene, propylene, butene, vinyl chloride, vinylidene
chloride and the like.
[0209] Vinyl ether or vinyl ester monomers:
[0210] CH.sub.2.dbd.CHOR, CH.sub.2.dbd.CHOCOR(R: hydrocarbon group
having 1 to 20 carbon atoms) and the like.
[0211] Allyl monomers:
[0212] CH.sub.2.dbd.CHCH.sub.2Cl, CH.sub.2.dbd.CHCH.sub.2OH,
CH.sub.2.dbd.CHCH.sub.2COOH,
[0213] CH.sub.2.dbd.CHCH.sub.2Br and the like.
[0214] Allyl ether monomers:
[0215] CH.sub.2.dbd.CHCH.sub.2OR
[0216] (R: hydrocarbon group having 1 to 20 carbon atoms),
[0217] CH.sub.2.dbd.CHCH.sub.2OCH.sub.2CH.sub.2COOH, 46
[0218] and the like.
[0219] Acrylic or methacrylic monomers:
[0220] Acrylic acid, methacrylic acid, acrylic acid esters,
methacrylic acid esters, maleic anhydride, maleic acid, maleic acid
esters and the like.
[0221] {circle over (5)} Structural units derived from alicyclic
monomers
[0222] A structural unit of an alicyclic monomer may be introduced
as a component copolymerizable with the structural unit M, more
preferably as the third component in addition to the structural
unit M and the structural unit of the above-mentioned
fluorine-containing ethylenic monomer or non-fluorine-containing
ethylenic monomer (the above-mentioned {circle over (3)} and
{circle over (4)}), which is preferable since a high glass
transition temperature can be obtained and hardness can be
increased.
[0223] Examples of the alicyclic monomer are norbornene derivatives
represented by: 47
[0224] wherein m is from 0 to 3; A, B, C and D are H, F, Cl, COOH,
CH.sub.2OH, a perfluoroalkyl having 1 to 5 carbon atoms or the
like, alicyclic monomers such as: 48
[0225] and derivatives thereof in which a substituent is
introduced.
[0226] In the curable fluorine-containing polymer of the present
invention, various combinations and proportions of the structural
units M (M1, M2 and M3) and A can be selected from the
above-mentioned examples depending on intended applications,
physical properties (particularly glass transition temperature,
hardness, etc.), functions (transparency and refractive index) and
the like.
[0227] The curable fluorine-containing polymer of the present
invention contains the structural unit M (M1, M2 or M3) as an
essential component and is characterized in that the structural
unit M itself has functions of maintaining a low refractive index
and imparting transparency to the polymer and functions of
imparting hardness, abrasion resistance, scratch resistance and
solvent resistance to the cured article by curing. Therefore even
if the curable fluorine-containing polymer of the present invention
contains a larger amount of the structural unit M or in the extreme
case, even if the polymer consists of the structural unit M (100%
by mole), the low refractive index can be maintained. Further the
curable fluorine-containing polymer of the present invention is
preferred since the cured article having a high curing
(crosslinking) density and the coating film having a high hardness
and excellent abrasion resistance and scratch resistance can be
obtained.
[0228] Also in the case of the copolymer of the present invention
comprising the structural unit M and the structural unit A of the
copolymerizable monomer, when the structural unit A is selected
from the above-mentioned examples, the polymer which provides the
cured article having a higher hardness (high glass transition
temperature) and a low refractive index can be obtained.
[0229] In the copolymer comprising the structural unit M and the
structural unit A, the proportion of the structural unit M may be
not less than 0.1% by mole based on the whole monomers constituting
the curable fluorine-containing polymer. It is preferable that the
proportion is not less than 2.0% by mole, more preferably not less
than 5% by mole, further preferably not less than 10% by mole in
order to obtain the cured article having a high hardness, excellent
abrasion resistance and scratch resistance and good chemical
resistance and solvent resistance by curing (crosslinking).
[0230] Particularly for the antireflection film application which
requires formation of a cured coating film having excellent scratch
and damage resistance, it is preferable that the structural unit M
is contained in an amount of not less than 10% by mole, preferably
not less than 20% by mole, more preferably not less than 50% by
mole.
[0231] The curable fluorine-containing polymer of the present
invention is preferable particularly for the antireflection film
application since a reflection reducing effect is not lowered even
if the proportion of the structural unit M is increased (or even if
the number of cure sites is increased).
[0232] Also in case of the antireflection film application, etc.
requiring transparency, preferred combinations and proportions of
the structural units M and A are those which can make the curable
fluorine-containing polymer non-crystalline.
[0233] Preferred fluorine-containing polymers for a coating
composition aiming at a low refractive index and a high hardness
are curable fluorine-containing polymers represented by the formula
(1-1).
-(M)-(A1)-(A2)- (1-1)
[0234] The structural unit M in the formula (1-1) is the
above-mentioned structural unit having an ethylenic carbon-carbon
double bond in its side chain, and the same structural units as the
above-mentioned preferable examples of the formulae (M1), (M2) and
(M3) can be used as the structural unit M.
[0235] The structural unit A1 is derived from a fluorine-containing
ethylenic monomer having functional group in its side chain and is
represented by the formula (A1): 49
[0236] wherein X.sup.11, X.sup.12 and X.sup.13 are H or F; X.sup.14
is H, F or CF.sub.3; h is 0, 1 or 2; i is 0 or 1; Rf.sup.4 is a
fluorine-containing alkylene group having 1 to 40 carbon atoms or a
fluorine-containing alkylene group having 2 to 100 carbon atoms and
ether bond; Z.sup.1 is selected from --OH, --CH.sub.2OH, --COOH,
carboxylic acid derivative, --SO.sub.3H, sulfonic acid derivative,
epoxy group and cyano group. The above-mentioned examples of the
structural unit A1 derived from the fluorine-containing ethylenic
monomer having functional group can be preferably used
similarly.
[0237] The structural unit A2 is derived from a fluorine-containing
ethylenic monomer not having functional group and is represented by
the formula (A2): 50
[0238] wherein X.sup.15, X.sup.16 and X.sup.18 are H or F; X.sup.17
is H, F or CF.sub.3; h1, i1 and j are 0 or 1; Z.sup.2 is H, F or
Cl; Rf.sup.5 is a fluorine-containing alkylene group having 1 to 20
carbon atoms or a fluorine-containing alkylene group having 2 to
100 carbon atoms and ether bond. The above-mentioned examples of
the structural unit A2 derived from the fluorine-containing
ethylenic monomer not having functional group can be preferably
used similarly. Among them, preferred is a structural unit derived
from at least one monomer selected from the group consisting of
tetrafluoroethylene, chlorotrifluoroethylene, vinylidene fluoride
and hexafluoropropylene.
[0239] It is preferable that the proportions of the structural
units M, A1 and A2 are from 0 to 90% by mole, from 0 to 99.9% by
mole and from 0 to 99.9% by mole, respectively and A1+A2 is from 10
to 99.9% by mole. It is particularly preferable that the
proportions of the structural units M, A1 and A2 are from 10 to 80%
by mole, from 1 to 60% by mole and from 20 to 85% by mole,
respectively and A1+A2 is from 20 to 90% by mole. When the
proportion of the structural unit M is too low, hardness of the
cured coating film tends to be lowered and strength thereof tends
to become insufficient. When the proportion of the structural unit
Al is too low, adhesion and coatability to a substrate and
solubility in a solvent tend to become insufficient. When the
proportion of the structural unit A2 is too low, there is a
tendency that coatability to a substrate, leveling property and
solubility in a solvent become insufficient.
[0240] In the fluorine-containing polymer comprising those
structural units M, A1 and A2, hardness, mechanical strength and
solvent resistance can be imparted to the cured coating film by a
cure site of the structural unit M. Also the functional group of
the structural unit A1 can impart adhesion to a substrate,
solubility in a solvent and good coatability (wettability and
leveling property) to the substrate. Further the structural unit A2
can impart, to the fluorine-containing polymer, a mechanical
strength, solubility in a solvent and good coatability to a
substrate.
[0241] Further since any of the structural units M, A1 and A2 have
many fluorine atoms, the above-mentioned functions can be imparted
while maintaining a low refractive index, and therefore the curable
fluorine-containing polymer is preferred as a coating agent for an
antireflection purpose.
[0242] The molecular weight of the curable fluorine-containing
polymer of the present invention can be selected, for example, in a
range of from 500 to 1,000,000 in number average molecular weight.
Preferred molecular weight is from 1,000 to 500,000, particularly
from 2,000 to 200,000.
[0243] When the molecular weight is to low, even after the curing,
mechanical properties are apt to be insufficient, and particularly
the cured article and cured coating film become fragile and are apt
to lack strength. If the molecular weight is too high, solubility
in a solvent is lowered, film forming property and leveling
property tend to be lowered particularly at forming a thin coating
film and storage stability of the curable fluorine-containing
polymer tends to be lowered. For coating applications, most
preferable number average molecular weight is selected in a range
of from 5,000 to 100,000.
[0244] In the curable fluorine-containing polymer of the present
invention, though various refractive indices can be selected
depending on kind and content of the structural unit M and kind of
the structural unit A to be used as case demands, it is preferable
that the refractive index of the curable fluorine-containing
polymer itself (before curing) is not more than 1.45, more
preferably not more than 1.40, particularly preferably not more
than 1.38. The refractive index changes depending on kinds of a
substrate and undercoating, but since the curing (crosslinking) can
be done while maintaining a low refractive index, the polymer can
be a preferable base polymer for an antireflection film.
[0245] Also it is preferable that the curable fluorine-containing
polymer is soluble in general-purpose solvents, for example, in at
least one of ketone solvents, acetic acid ester solvents, alcohol
solvents and aromatic solvents or in solvent mixtures containing at
least one of the above-mentioned general-purpose solvents.
[0246] When the polymer is soluble in general-purpose solvents, it
is preferable because film forming property and homogeneity are
excellent in coating application, particularly in case of forming a
thin antireflection film of about 0.1 .mu.m thick on various
transparent films and displaying substrates. The polymer is also
advantageous from the viewpoint of productivity in forming an
antireflection film.
[0247] In order to obtain the curable fluorine-containing polymer
of the present invention, any of
[0248] {circle over (1)} a method of previously synthesizing a
monomer having the functional group Y.sup.1 and then
polymerizing,
[0249] {circle over (2)} a method of once synthesizing a polymer
having another functional group and then converting the functional
group by high molecular reaction, thus introducing the functional
group Y.sup.1 into the polymer, or the like method can be
employed.
[0250] In the method {circle over (1)}, in order to obtain the
curable fluorine-containing polymer of the present invention having
a carbon-carbon double bond in its side chain without reacting
(curing) the carbon-carbon double bond at an end of its side chain,
it is necessary to change reactivity of two kinds of double bonds
(a double bond becoming a trunk chain and a double bond becoming a
side chain) in a (co)polymerizable monomer and thereby make only
one of the double bonds participate in the polymerization. In such
a method, it is difficult to select the polymerization conditions
to obtain the curable fluorine-containing polymer of the present
invention having a double bond in its side chain, and also it is
difficult to use a monomer which gives a high curing reactivity of
the double bond in the side chain to the obtained curable
polymer.
[0251] On the contrary, the method {circle over (2)} is a
preferable method since it is easy to obtain the curable
fluorine-containing polymer of the present invention without curing
reaction and also from the point that a carbon-carbon double bond
having a high curing reactivity can be introduced to its side
chain.
[0252] Among the methods {circle over (2)}, there is preferably
employed, for example, a method of obtaining the curable
fluorine-containing polymer of the present invention by
synthesizing the fluorine-containing polymer comprising the
structural unit N of fluorine-containing monomer having hydroxyl or
an organic group Y.sup.3 having hydroxyl and as case demands, the
structural unit B of monomer copolymerizable with N, and then
reacting the polymer with an unsaturated carboxylic acid or its
derivative to introduce a carbon-carbon double bond to an end of a
side chain of the polymer.
[0253] Therefore the second of the present invention relates to the
process for preparing the curable fluorine-containing polymer,
which is characterized by esterification reaction, with an
unsaturated carboxylic acid or its derivative, of the
fluorine-containing polymer having hydroxyl and represented by the
formula (2):
N.paren close-st.B.paren close-st. (2)
[0254] in which the structural unit N is a structural unit having
hydroxyl and derived from a fluorine-containing ethylenic monomer
and is represented by the formula (N): 51
[0255] wherein X.sup.1 and X.sup.2 are the same or different and
each is H or F; X.sup.3 is H, F, CH.sub.3 or CF.sub.3; X.sup.4 and
X.sup.5 are the same or different and each is H, F or CF.sub.3;
Rf.sup.1 is an organic group in which 1 to 3 of Y.sup.5 (Y.sup.5 is
hydroxyl or a monovalent organic group having 1 to 10 carbon atoms
and hydroxyl) are bonded to a fluorine-containing allyl group
having 1 to 40 carbon atoms or a fluorine-containing allyl group
having 2 to 100 carbon atoms and ether bond; a is 0 or an integer
of from 1 to 3; b and c are the same or different and each is 0 or
1,
[0256] the structural unit B is a structural unit derived from
monomer copolymerizable with the fluorine-containing ethylenic
monomer having hydroxyl and represented by the above-mentioned
formula (N), and the structural unit N and the structural unit B
are contained in amounts of from 0.1 to 100% by mole and from 0 to
99.9% by mole, respectively.
[0257] In the above-mentioned process for preparing the curable
fluorine-containing polymer of the present invention, examples of
the preferable structural unit N of the fluorine-containing polymer
having hydroxyl which is a precursor represented by the formula (2)
are structures which correspond to the above-exemplified respective
structural units M of the curable fluorine-containing polymer and
have the Y.sup.5 having OH group instead of the Y.sup.1 having a
carbon-carbon double bond. Those structural units can be used
preferably. As the structural unit B, there can be preferably used
the same structural units as the above-mentioned structural unit
A.
[0258] The unsaturated carboxylic acid or its derivative which is
reacted with the fluorine-containing polymer having hydroxyl may be
any of carboxylic acids or derivatives thereof having a
carbon-carbon double bond at an end thereof. Particularly preferred
are .alpha.,.beta.-unsaturated carboxylic acids or derivatives
thereof (f=0).
[0259] Examples thereof are, for instance, carboxylic acids
represented by: 52
[0260] wherein R is H, CH.sub.3, F, CF.sub.3 or Cl, or anhydrides
thereof, acid halides represented by: 53
[0261] wherein R is as defined above, X is Cl or F, maleic acid,
maleic anhydride, maleic acid monoalkylester and the like.
[0262] Among them, unsaturated carboxylic acid halides are
preferred since the reaction can be carried out at room temperature
and gelling of a prepared polymer can be prevented.
[0263] Particularly preferred are: 54
[0264] The method of reacting the fluorine-containing polymer
having hydroxyl with .alpha.,.beta.-unsaturated carboxylic acid
halide is not limited particularly and is usually carried out by
dissolving the fluorine-containing polymer having hydroxyl in a
solvent and mixing the .alpha.,.beta.-unsaturated carboxylic acid
halide thereto at a temperature of from about -20.degree. C. to
about 40.degree. C. with stirring.
[0265] In the reaction, through the reaction conditions, HCl and HF
are produced and therefore it is desirable to add a proper base for
capturing them. Examples of the base are tertiary amines such as
pyridine, N,N-dimethylaniline, tetramethylurea and triethylamine,
magnesium metal and the like. Also an inhibitor may be present to
prevent a polymerization reaction of the carbon-carbon double bonds
in the starting .alpha.,.beta.-unsaturated carboxylic acid and the
obtained curable fluorine-containing polymer during the
reaction.
[0266] Examples of the inhibitor are hydroquinone, t-butyl
hydroquinone, hydroquinone monomethylether and the like.
[0267] The fluorine-containing polymer having hydroxyl before the
reaction with the unsaturated carboxylic acid or its derivative can
be obtained by (co)polymerizing through known method the respective
component units such as the ethylenic monomer (N) having hydroxyl
and the monomer (B) when used as a copolymerizable component. For
the polymerization, radical polymerization method, anion
polymerization method, cation polymerization method and the like
can be employed. Among them, the radical polymerization method is
preferably used from the viewpoint that each monomer exemplified to
obtain the polymer having hydroxyl of the present invention has
good radial polymerizability, control of composition and molecular
weight is easy and production in an industrial scale is easy.
[0268] In order to initiate the radical polymerization, means for
initiation is not limited particularly as far as the polymerization
proceeds radically. The polymerization is initiated, for example,
with an organic or inorganic radical polymerization initiator,
heat, light, ionizing radiation or the like. The polymerization can
be carried out by solution polymerization, bulk polymerization,
suspension polymerization, emulsion polymerization or the like. The
molecular weight is controlled by the contents of the monomers to
be used for the polymerization, the content of the polymerization
initiator, the content of a chain transfer agent, temperature, etc.
The components of the copolymer can be controlled by the starting
monomer components.
[0269] The third of the present invention relates to the
composition comprising a curable fluorine-containing polymer. One
of the compositions of the present invention is the curable
fluorine-containing resin composition comprising:
[0270] (a) a curable fluorine-containing polymer and
[0271] (b) an active energy curing initiator which initiates curing
with active energy.
[0272] The curable fluorine-containing polymer (a) for the
composition of the present invention is the above-mentioned curable
fluorine-containing polymer having a carbon-carbon double bond in
its side chain, and preferred examples thereof are the same as
those exemplified above.
[0273] The active energy curing initiator (b) which initiates
curing with active energy functions as a catalyst which generates
radical or cation only by irradiation of, for example, an
electromagnetic wave having a wavelength of not more than 350 nm,
namely ultraviolet light, electron beam, X-ray, .gamma.-ray and the
like and initiates curing (crosslinking reaction) of the
carbon-carbon double bond of the curable fluorine-containing
polymer. Usually curing initiators which generate radical or cation
by irradiation of ultraviolet light, particularly those generating
radical are used.
[0274] This curable fluorine-containing resin composition can
initiate a curing reaction easily with the above-mentioned active
energy, does not require heating at high temperatures and can be
subjected to the curing reaction at low temperatures. Therefore the
composition is preferred from the point that it can be used on
substrates, for example, transparent resin substrates which have
low heat resistance and easily undergo deformation, degrading and
coloring due to heat.
[0275] In the composition of the present invention, the curing
initiator (b) which initiates curing with active energy is
optionally selected depending on kind of the carbon-carbon double
bond (radical-reactivity or cation-reactivity) in the side chain of
the curable fluorine-containing polymer (a), kind (wavelength
range, etc.) of the active energy, intensity of irradiation, etc.
Generally examples of the initiator which functions to initiate
curing of the curable fluorine-containing polymer (a) having a
radical-reactive carbon-carbon double bond with active energy in an
ultraviolet region are, for instance, those mentioned below.
[0276] Acetophenone Initiators
[0277] Acetophenone, chloroacetophenone, diethoxyacetophenone,
hydroxyacetophenone, .alpha.-aminoacetophenone,
hydroxypropiophenone,
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinepropane-1-one and the
like.
[0278] Benzoin Initiators
[0279] Benzoin, benzoinmethylether, benzoinethylether,
benzoinisopropylether, benzoinisobutylether, benzyldimethylketal
and the like.
[0280] Benzophenone Initiators
[0281] Benzophenone, benzoyl benzoate, methyl-o-benzoylbenzoate,
4-phenylbenzophenone, hydroxybenzophenone,
hydroxy-propylbenzophenone, acrylated benzophenone, Michler's
ketone and the like.
[0282] Thioxanthone Initiators
[0283] Thioxanthone, chlorothioxanthone, methylthioxanthone,
diethylthioxanthone, dimethylthioxanthone and the like.
[0284] Other Initiators
[0285] Benzyl, .alpha.-acyloxime ester, acylphosphine oxide,
glyoxyester, 3-ketocoumaran, 2-ethylanthraquinone, camphorquinone,
anthraquinone and the like.
[0286] Depending on kind of the fluorine-containing polymer or kind
of the above-mentioned active energy curing initiator, there is a
case where compatibility between the polymer and the initiator is
not good and the coating composition itself or a coating film after
coating becomes turbid in white and transparency and curing
reactivity are lowered (Experimental Example 21(1)).
[0287] The present inventors have found that compatibility between
the polymer and the initiator can be improved by introducing
fluorine atom or an organic group having fluorine atom to the
active energy curing initiator.
[0288] Concretely preferred are initiators having a
fluorine-containing alkyl group, a fluorine-containing alkylene
group, a fluorine-containing alkyl group having ether bond or a
fluorine-containing alkylene group having ether bond. For example,
there are an initiator in which a fluorine-containing carboxylic
acid (polycarboxylic acid) or the like having the above-mentioned
fluorine-containing organic group is introduced into an initiator
having OH group by ester bonding (Experimental Example 18) and an
initiator in which a fluorine-containing carboxylic acid
(polycarboxylic acid) or the like is introduced into an initiator
having amino group by amide bonding.
[0289] The introduction of the fluorine-containing organic group to
the initiator is preferred since even in the fluorine-containing
polymer having a high fluorine content, compatibility is good and
curing reactivity and transparency of the coating film can be
improved (Experimental Example 21(1)).
[0290] Also as case demands, an auxiliary for photo-initiation such
as amines, sulfones or sulfines may be added.
[0291] Also examples of the initiator which initiates curing of the
curable fluorine-containing polymer. (a) having a cation-reactive
carbon-carbon double bond are those mentioned below.
[0292] Onium Salts
[0293] Iodonium salt, sulfonium salt, phosphonium salt, diazonium
salt, ammonium salt, pyridinium salt and the like.
[0294] Sulfone Compounds
[0295] .beta.-ketoester, .beta.-sulfonylsulfone, .alpha.-diazo
compounds thereof and the like.
[0296] Sulfonic Acid Esters
[0297] Alkylsulfonic acid ester, haloalkylsulfonic acid ester,
arylsulfonic acid ester, iminosulfonate and the like.
[0298] Others
[0299] Sulfone imide compounds, diazomethane compounds and the
like.
[0300] Also in those cation-reactive active energy curing
initiators, compatibility thereof with the fluorine-containing
polymer can be improved by introducing fluorine atom or a
fluorine-containing organic group to the initiators like the
above-mentioned case.
[0301] Another embodiment of the curable fluorine-containing resin
composition of the present invention is one using a solvent, which
is preferable from the point that the composition dissolved and
dispersed in the solvent can be coated on various substrates to
form a coating film and the coating film can be effectively cured
by irradiation with active energy or the like to obtain a cured
coating film.
[0302] Namely, the fluorine-containing resin composition for
coating of the present invention is the composition comprising:
[0303] (a) a curable fluorine-containing polymer,
[0304] (b) an active energy curing initiator and
[0305] (c) a solvent.
[0306] There can be preferably used the same curable
fluorine-containing polymer (a) and active energy curing initiator
(b) as in the above-mentioned curable fluorine-containing resin
composition.
[0307] The solvent (c) is not limited particularly as far as the
curable fluorine-containing polymer (a), active energy curing
initiator (b) and additives such as a curing agent, leveling agent
and light-stabilizer to be added as case demands are uniformly
dissolved and dispersed therein. Particularly preferred is the
solvent which uniformly dissolves the curable fluorine-containing
polymer (a). This embodiment using the solvent is preferable from
the point that a coating film having a high transparency and
uniformity can be obtained in high productivity particularly in the
antireflection film application, etc. where a thin coating film
(about 0.1 .mu.m thick) is required.
[0308] Examples of the solvent (c) are, for instance, cellosolve
solvents such as methyl cellosolve, ethyl cellosolve, methyl
cellosolve acetate and ethyl cellosolve acetate; ester solvents
such as diethyl oxalate, ethyl pyruvate, ethyl-2-hydroxybutyrate,
ethyl acetoacetate, butyl acetate, amyl acetate, ethyl butyrate,
butyl butyrate, methyl lactate, ethyl lactate, methyl
3-methoxypropionate, ethyl 3-methoxypropionate, methyl
2-hydroxyisobutyrate and ethyl 2-hydroxyisobutyrate; propylene
glycol solvents such as propylene glycol monomethyl ether,
propylene glycol monoethyl ether, propylene glycol monobutyl ether,
propylene glycol monomethyl ether acetate, propylene glycol
monoethyl ether acetate, propylene glycol monobutyl ether acetate
and dipropylene glycol dimethyl ether; ketone solvents such as
2-hexanone, cyclohexanone, methyl amino ketone and 2-heptanone;
alcohol solvents such as methanol, ethanol, propanol, isopropanol
and butanol; aromatic hydrocarbons such as toluene and xylene; a
solvent mixture of two or more thereof and the like.
[0309] Also in order to enhance solubility of the curable
fluorine-containing polymer (a), a fluorine-containing solvent may
be used as case demands.
[0310] Examples of the fluorine-containing solvent are, for
instance, CH.sub.3CCl.sub.2F (HCFC-141b), a mixture of
CF.sub.3CF.sub.2CHCl.sub.2 and CClF.sub.2CF.sub.2CHClF (HCFC-225),
perfluorohexane, perfluoro(2-butyltetrahydrofuran),
methoxy-nonafluorobutane, 1,3-bistrifluoromethylbenzene, and in
addition, fluorine-containing alcohols such as:
[0311] H(CF.sub.2CF.sub.2.paren close-st..sub.nCH.sub.2OH (n: an
integer of from 1 to 3),
[0312] F(CF.sub.2.paren close-st..sub.nCH.sub.2OH (n: an integer of
from 1 to 5) and
[0313] (CF.sub.3.paren close-st..sub.2CHOH,
[0314] benzotrifluoride, perfluorobenzene,
perfluoro(tributylamine), ClCF.sub.2CFClCF.sub.2CFCl.sub.2 and the
like.
[0315] Those fluorine-containing solvents may be used solely, in a
mixture of two or more thereof or in a mixture of one or more of
the fluorine-containing solvents and non-fluorine-containing
solvents.
[0316] Among them, ketone solvents, acetic acid ester solvents,
alcohol solvents and aromatic solvents are preferred from the
viewpoint of coatability and productivity of a coating film.
[0317] The present inventors have found that at dissolving the
curable fluorine-containing polymer, when the fluorine-containing
alcohol solvent is mixed to the above-mentioned general-purpose
solvent, a leveling property of the polymer coating film after the
coating on a substrate and drying can be improved.
[0318] This effect of improving a leveling property is high in the
case of resin substrates, particularly an acrylic resin, cellulose
resin, polyethylene terephthalate, polycarbonate and polyolefin and
is exhibited significantly particularly in the case of a
polyethylene terephthalate substrate (Experimental Examples 44 and
45).
[0319] The fluorine-containing alcohol to be added may be one which
has a boiling point of not less than 50.degree. C., preferably not
less than 80.degree. C. and dissolves the curable
fluorine-containing polymer.
[0320] Examples thereof are, for instance,
[0321] HCF.sub.2CF.sub.2.paren close-st..sub.nCH.sub.2OH (n is an
integer of from 1 to 4),
[0322] FCF2.paren close-st..sub.nCH.sub.2OH (n is an integer of
from 1 to 6),
[0323] (CF.sub.3.paren close-st..sub.2CHOH
[0324] and the like.
[0325] Though the fluorine-containing alcohol may be used solely as
a solvent, it is effective to mix the fluorine-containing alcohol
in addition to the above-mentioned general purpose solvent such as
ketone solvent, acetic acid ester solvent, non-fluorine-containing
alcohol solvent, aromatic solvent or the like.
[0326] When the fluorine-containing alcohol is mixed, an adding
amount thereof is not less than 1% by weight, preferably not less
than 5% by weight, more preferably not less than 10% by weight,
particularly from 10% by weight to 30% by weight based on the whole
solvents.
[0327] Further in the present invention, as case demands, a curing
agent may be added to the curable fluorine-containing resin
composition comprising the curable fluorine-containing polymer (a)
and the active energy curing initiator (b) and also to the
fluorine-containing resin composition for coating further
containing the solvent (c).
[0328] Preferred curing agents are those which have at least one
carbon-carbon unsaturated bond and can be polymerized with radical
or an acid. Examples thereof are concretely radically polymerizable
monomers such as an acrylic monomer and cationically polymerizable
monomers such as a vinyl ether monomer. Those monomers may be
monofunctional monomers having one carbon-carbon double bond or
polyfunctional monomers having two or more carbon-carbon double
bonds.
[0329] Those so-called curing agents having a carbon-carbon
unsaturated bond react by radical or cation generated by reaction
of the active energy curing initiator (b) in the composition of the
present invention with the active energy such as light and can be
crosslinked with the carbon-carbon double bond in the side chain of
the curable fluorine-containing polymer (a) in the composition of
the present invention by copolymerization.
[0330] Examples of the monofunctional acrylic monomer are acrylic
acid, acrylic acid esters, methacrylic acid, methacrylic acid
esters, .alpha.-fluoroacrylic acid, .alpha.-fluoroacrylic acid
esters, maleic acid, maleic anhydride, maleic acid esters and
(meth)acrylic acid esters having epoxy, hydroxyl, carboxyl or the
like.
[0331] Among them, preferred are acrylate monomers having a
fluoroalkyl group to maintain a low refractive index of the cured
article. For example, preferred are compounds represented by the
formula: 55
[0332] wherein X is H, CH.sub.3 or F; Rf is a fluorine-containing
alkyl group having 2 to 40 carbon atoms or a fluorine-containing
alkyl group having 2 to 100 carbon atoms and ether bond.
[0333] Examples thereof are: 56
[0334] and the like.
[0335] As the polyfunctional acrylic monomer, there are generally
known compounds obtained by replacing hydroxyl groups of polyhydric
alcohols such as diol, triol and tetraol with acrylate groups,
methacrylate groups or .alpha.-fluoroacrylate groups.
[0336] Examples thereof are compounds obtained by replacing two or
more hydroxyl groups of polyhydric alcohols such as 1,3-butanediol,
1,4-butanediol, 1,6-hexanediol, diethylene glycol, tripropylene
glycol, neopentyl glycol, trimethylol propane, pentaerythritol and
dipentaerythritol with any of acrylate groups, methacrylate groups
or .alpha.-fluoroacrylate groups.
[0337] Also there can be used polyfunctional acrylic monomers
obtained by replacing two or more hydroxyl groups of polyhydric
alcohols having a fluorine-containing alkyl group, a
fluorine-containing alkyl group having ether bond, a
fluorine-containing alkylene group or a fluorine-containing
alkylene group having ether bond with acrylate groups, methacrylate
groups or a-fluoroacrylate groups. Those monomers are preferred
particularly from the point that a low refractive index of the
cured article can be maintained.
[0338] Preferable examples thereof are compounds having structures
obtained by replacing two or more hydroxyl groups of
fluorine-containing polyhydric alcohols represented by the
formulae: 57
[0339] (Rf is a fluorine-containing alkyl group having 1 to 40
carbon atoms) 58
[0340] (Rf is a fluorine-containing alkyl group having 1 to 40
carbon atoms or a fluorine-containing alkyl group having 1 to 40
carbon atoms and ether bond, R is H or an alkyl group having 1 to 3
carbon atoms)
[0341] HO--CH.sub.2--Rf'--CH.sub.3OH, 59
[0342] (Rf' is a fluorine-containing alkylene group having 1 to 40
carbon atoms or a fluorine-containing alkylene group having 1 to 40
carbon atoms and ether bond, R is H or an alkyl group having 1 to 3
carbon atoms) with acrylate groups, methacrylate groups or
.alpha.-fluoroacrylate groups.
[0343] When those exemplified monofunctional and polyfunctional
acrylic monomers are used as the curing agent for the composition
of the present invention, particularly preferred are
.alpha.-fluoroacrylate compounds from the viewpoint of good curing
reactivity.
[0344] In the composition of the present invention, an adding
amount of the active energy curing initiator (b) is optionally
selected depending on the content of the carbon-carbon double bonds
in the curable fluorine-containing polymer (a), an amount of the
curing agent and further kinds of the initiator and active energy
and an amount of irradiation energy (intensity and time) and also
depending on whether or not the above-mentioned curing agent is
used. When the curing agent is not used, the amount of the
initiator is from 0.01 to 30 parts by weight, preferably from 0.05
to 20 parts by weight, most preferably from 0.1 to 10 parts by
weight based on 100 parts by weight of the curable
fluorine-containing polymer (a).
[0345] Concretely the amount of the initiator is from 0.05 to 50%
by mole, preferably from 0.1 to 20% by mole, most preferably from
0.5 to 10% by mole based on the content (the number of moles) of
the carbon-carbon double bonds contained in the curable
fluorine-containing polymer (a).
[0346] When the curing agent is used, the amount of the initiator
is from 0.05 to 50% by mole, preferably from 0.1 to 20% by mole,
most preferably from 0.5 to 10% by mole based on the total number
of moles including the content (number of moles) of the
carbon-carbon double bonds contained in the curable
fluorine-containing polymer (a) and the number of moles of the
carbon-carbon unsaturated bonds of the curing agent.
[0347] When the curing agent is used, the amount of the curing
agent is optionally selected depending on intended hardness and
refractive index, kind of the curing agent, the content of curable
groups of the curable fluorine-containing polymer, etc. The amount
is desirably from 1 to 80% by weight, preferably from 5 to 70% by
weight, more preferably from 10 to 50% by weight based on the
curable fluorine-containing polymer. If the amount of the curing
agent is too large, there is a tendency that the refractive index
is increased, which is not preferable.
[0348] The content of the solvent (c) in the fluorine-containing
resin composition for coating of the present invention is
optionally selected depending on kinds of solids to be dissolved,
the amount of the curing agent, kind of a substrate, intended
coating thickness, etc. and also depending on whether or not the
curing agent is used. It is preferable to decide the amount of the
solvent so that a concentration of the whole solids in the
composition becomes from 0.5 to 70% by weight, preferably from 1 to
50% by weight.
[0349] To the composition of the present invention may be added
various additives as case demands in addition to the
above-mentioned compounds.
[0350] Examples of the additives are, for instance, a leveling
agent, viscosity control agent, light-stabilizer, moisture
absorbing agent, pigment, dye, reinforcing agent and the like.
[0351] Also to the composition of the present invention can be
added fine particles of inorganic compounds to increase hardness of
the cured article.
[0352] The fine particles of inorganic compound are not limited
particularly. Preferred are compounds having a refractive index of
not more than 1.5. Desirable fine particles are magnesium fluoride
(refractive index: 1.38), silicon oxide (refractive index: 1.46),
aluminum fluoride (refractive index: from 1.33 to 1.39), calcium
fluoride (refractive index: 1.44), lithium fluoride (refractive
index: from 1.36 to 1.37), sodium fluoride (refractive index: from
1.32 to 1.34), thorium fluoride (refractive index: from 1.45 to
1.50) and the like. It is desirable that a particle size of the
fine particles is sufficiently small as compared with wavelengths
of visible light in order to ensure transparency of the low
refractive index material. The particle size is preferably not more
than 100 nm, particularly preferably not more than 50 nm.
[0353] When the fine particles of inorganic compound are used, it
is desirable to use them in the form of organic sol previously
dispersed in an organic dispersion in order not to lower dispersion
stability in the composition and adhesion in the low refractive
index material. Further in order to enhance dispersion stability of
the fine particles of inorganic compound in the composition and
adhesion in the low refractive index material, surfaces of the fine
particles of inorganic compound can be previously modified with
various coupling agents. Examples of the coupling agent are, for
instance, organosilicon compounds; metal alkoxides such as
aluminum, titanium, zirconium, antimony and a mixture thereof;
salts of organic acids; coordination compounds bonded with a
coordinative compound; and the like.
[0354] In the fluorine-containing resin composition for coating of
the present invention, the curable fluorine-containing polymer (a)
or additives may be in either form of dispersion or solution in the
solvent (c). In order to form a uniform thin coating film and
enable the coating film to be formed at relatively low
temperatures, the form of uniform solution is preferred.
[0355] For the coating, known coating methods can be employed as
far as a coating thickness can be controlled.
[0356] For example, there can be employed a roll coating method,
gravure coating method, micro-gravure coating method, flow coating
method, bar coating method, spray coating method, dye coating
method, spin coating method, dip coating method and the like. The
coating method can be selected in consideration of kind and shape
of a substrate, productivity, controllability of a coating
thickness, etc.
[0357] The curable resin composition of the present invention
comprising the curable fluorine-containing polymer (a) and the
active energy curing initiator (b) and the coating film obtained by
coating the fluorine-containing resin composition for coating of
the present invention on a substrate by the above-mentioned coating
method and then drying can be photo-cured by irradiation of active
energy rays such as ultraviolet light, electron beam or radioactive
ray.
[0358] By the photo-curing, the carbon-carbon double bonds in the
curable fluorine-containing polymer (a) of the present invention
are polymerized between the molecules, and the carbon-carbon double
bonds in the polymer decrease or disappear. As a result, hardness
of the resin becomes high, a mechanical strength is increased,
abrasion resistance and scratch resistance are increased and
further the composition not only becomes insoluble in a solvent in
which the composition is soluble before the curing but also becomes
insoluble in many other kinds of solvents.
[0359] The fourth of the present invention relates to the
antireflection film.
[0360] Namely, the antireflection film is the cured coating film of
the fluorine-containing prepolymer which has a coating thickness of
from 0.03 to 0.5 .mu.m and is characterized in that the prepolymer
has:
[0361] (1) a carbon-carbon unsaturated bond at an end of its side
chain, and
[0362] (2) a refractive index of not more than 1.40.
[0363] This invention was completed based on the findings of the
present inventors that when the fluorine-containing prepolymer
which has a carbon-carbon unsaturated bond capable of curing
(crosslinking) and is low in a refractive index is coated on a
transparent substrate in a specific coating thickness and is cured,
an antireflection film having a reflection reducing effect and in
addition, a high hardness, abrasion resistance and scratch
resistance can be obtained. When such a prepolymer is used,
coatability (smoothness and uniformity of a coating thickness) is
good, a low molecular weight monomer component is hard to remain in
the coating film after the curing, and therefore the coating film
is free from feeling of tackiness on its surface and has excellent
characteristics.
[0364] The curing can be carried out with heat and light (in a
system containing an initiator). However when the antireflection
film is provided on a transparent resin substrate, applying high
temperatures on the substrate is not preferable because thermal
deterioration and thermal deformation of the substrate are apt to
occur. Therefore the curing with light is preferred, and it is
preferable that the fluorine-containing prepolymer has a
carbon-carbon unsaturated bond capable of photo-curing (for
example, photo-polymerizing).
[0365] For obtaining an antireflection film by photo-curing a
fluorine-containing prepolymer, there is usually employed a method
of obtaining a cured coating film by preparing a coating
composition comprising:
[0366] (d) the above-mentioned fluorine-containing prepolymer,
[0367] (e) an active energy curing initiator, and
[0368] (f) a solvent,
[0369] coating the coating composition on a substrate, forming a
coating film (not-cured) by drying and then irradiating the coating
film with active energy ray such as ultraviolet light, electron
beam, radioactive ray or the like. The light irradiation may be
carried out in either of air stream and inert gas stream such as
nitrogen gas. Particularly the light irradiation in an inert gas
stream is preferred from the viewpoint of good curing reactivity,
and a coating film having a higher hardness can be obtained.
[0370] As the fluorine-containing prepolymer (d) for the
antireflection film of the present invention, any of
fluorine-containing prepolymers can be used as far as they have a
reactive carbon-carbon unsaturated bond in the side chain thereof.
From the viewpoint of good reactivity, an ethylenic carbon-carbon
double bond is preferred.
[0371] Particularly preferred is a combination use of the
fluorine-containing prepolymer (d1) having a radically
polymerizable ethylenic carbon-carbon double bond and the initiator
(e) generating radical by irradiation of active energy ray from the
point that the polymerization reaction occurs rapidly, a degree of
polymerization is high and the curing can be easily carried
out.
[0372] Also the fluorine-containing prepolymer (d2) having an
acid-polymerizable carbon-carbon double bond can be used in
combination with an initiator generating an acid by irradiation of
active energy ray, which is preferable from the point that the
curing reaction is less affected by air (oxygen), etc. at the time
of light irradiation.
[0373] The fluorine-containing prepolymer to be used for the
antireflection film of the present invention is preferably the same
as the above-mentioned curable fluorine-containing polymers, and
among the above-mentioned examples of the curable polymer, those
which have a high transparency, are non-crystalline and have a
refractive index of not more than 1.40, preferably not more than
1.38 are selected. Further among them, it is preferable to
optionally select the polymers depending on intended hardness, kind
of a substrate, coating method, coating conditions, coating
thickness, uniformity of a coating film, adhesion to the substrate,
etc.
[0374] As the active energy curing initiator (e) to be used for the
antireflection film of the present invention, the same initiators
as exemplified in the above-mentioned curable fluorine-containing
resin composition can be used. Kind and an amount of the initiator
can be optionally selected in the above-mentioned range in
consideration of kind (reactivity, content) of the carbon-carbon
unsaturated bond in the fluorine-containing prepolymer, curing
conditions, a pot life of the coating, etc.
[0375] As the solvent (f), there can be used those exemplified in
the above-mentioned curable resin composition for coating. Kind and
an amount of the solvent (f) are optionally selected from the
above-mentioned examples depending on intended coatability, film
forming property, uniformity of a coating thickness, productivity
in coating, etc. Among the solvents, those which cause dissolving
and swelling of the transparent substrate are not preferred.
[0376] Particularly preferred are those selected from ketone
solvents, acetic acid ester solvents, alcohol solvents and aromatic
hydrocarbon solvents.
[0377] In the antireflection film of the present invention, it is
natural that the same curing agent (g) as mentioned above may be
used together with the curable fluorine-containing prepolymer (d).
The use of the curing agent can make hardness of the cured coating
film higher.
[0378] Kind and an amount of the curing agent (g) to be used
preferably are the same as those mentioned in the above-mentioned
fluorine-containing resin composition for coating.
[0379] It is preferable that after coating of the coating
composition and curing of the fluorine-containing prepolymer, the
cured article (coating film) has a refractive index of not more
than 1.49, more preferably not more than 1.45, further preferably
not more than 1.40. Most preferred is a refractive index of not
more than 1.38. A lower refractive index is more advantageous from
the viewpoint of a reflection reducing effect.
[0380] A preferable coating thickness of the antireflection film to
be used on various substrates varies with the refractive indices of
the film and substrate and is selected in the range of from 0.03 to
0.5 .mu.m, preferably from 0.07 to 0.2 .mu.m, more preferably from
0.08 to 0.12 .mu.m. When the coating thickness is too small, there
is a tendency that reduction of reflectance due to light
interference in visible light becomes insufficient. When the
coating thickness is too large, since the reflectance comes to
depend only on a reflection nearly at an interface between air and
film, there is a tendency that reduction of reflectance due to
light interference in visible light becomes insufficient. It is
particularly preferable that a proper coating thickness is set so
that a wavelength exhibiting a minimum reflectance of an
antireflection-treated article provided with the antireflection
film is usually from 420 to 720 nm, preferably from 520 to 620
nm.
[0381] The fifth of the present invention relates to the
antireflection-treated article obtained by applying the
antireflection film on a substrate.
[0382] Kind of the article, namely kind of the substrate which is
provided with the antireflection film is not limited particularly.
Examples thereof are, for instance, inorganic materials such as
glass, stone, concrete and tile; synthetic resins, namely vinyl
chloride resin, polyethylene terephthalate, cellulose resins such
as triacetyl cellulose, polycarbonate resin, polyolefin resin,
acrylic resin, phenol resin, xylene resin, urea resin, melamine
resin, diallyl phthalate resin, furan resin, amino resin, alkyd
resin, urethane resin, vinyl ester resin and polyimide resin;
metals such as iron, aluminum and copper; wood, paper, printed
matter, printing paper, picture, etc. When a certain portion of the
article other than a specific portion thereof is provided with the
antireflection film and the shape of the specific portion is lifted
up by a reflecting light, a decorative effect of the article can be
enhanced.
[0383] The antireflection film can be preferably provided
particularly on the transparent resin substrates such as an acrylic
resin, polycarbonate, cellulose rein, polyethylene terephthalate
and polyolefin resin, and a reflection reducing effect can be
exhibited effectively.
[0384] The present invention is effectively applied on the
following articles.
[0385] Optical parts such as prism, lens sheet, polarizing plate,
optical filter, lenticular lens, Fresnel lens, screen of rear
projection display, optical fiber and optical coupler;
[0386] Transparent protection plates represented by glass for show
window, glass for display case, cover for advertisement and cover
for photo-stand;
[0387] Protection plates for CRT, liquid crystal display, plasma
display and rear projection display;
[0388] Optical recording media such as magnetic optical disk, read
only type optical disks such as CD, LD and DVD, phase transition
type optical disk such as PD and hologram recorder;
[0389] Photolithography-related members for production of
semiconductors such as photoresist, photomask, pellicle and
reticule;
[0390] Protection covers for light emitters such as halogen lamp,
fluorescent lamp and incandescent lamp; and
[0391] Sheet or film for adhering to the above-mentioned
articles.
[0392] The antireflection film of the present invention may be
formed into a cured coating film having a thickness of about 0.1
.mu.m by applying a solution of the fluorine-containing prepolymer
(d) directly on a substrate and then irradiating the coating film
with light, or the antireflection film may be formed, as a top
coat, on one or plural undercoat layers formed on the
substrate.
[0393] The effects of the undercoat are roughly classified into
three, namely an increase of scratch resistance of the top coat,
protection of the substrate and an increase of a reflection
reducing effect by providing the layers having a refractive index
higher than that of the substrate. In order to increase scratch
resistance of the top coat, a self-repairing undercoat mentioned in
JP7-168005A may be used. Also for the protection of the substrate,
a coating generally called a hard coat may be used. Examples of the
hard coat are cured articles from curable acrylic resin, epoxy
resin and silicon alkoxide compounds, cured articles from metal
alkoxide compounds and the like. A heat curing method can be
applied on all of them. For the acrylic resin and epoxy resin, a
photo-curing method (ultraviolet light) is preferred from the
viewpoint of productivity.
[0394] With respect to CRT and plasma display, static electricity
easily deposits on the surface thereof due to characteristics of
equipment. Therefore it is preferable to mix, to the undercoat
layer and/or top coat layer as mentioned above, an additive
imparting electric conductivity. Examples of the additive are
polymers having ionic group such as --COO--, --NH.sub.2,
--NH.sub.3.sup.+, --NR.sup.11R.sup.12R.sup.13, in which R.sup.11
R.sup.12 and R.sup.13 are, for example, methyl, ethyl, n-propyl,
n-butyl or the like, or --SO.sub.3--, silicone compounds, inorganic
electrolytes (for example, NaF, CaF.sub.2, etc.) and the like.
[0395] Also in order to prevent adhesion of dust, it is preferable
to add an anti-static agent to the undercoat layer of the
antireflection film and/or top coat layer. Examples of the additive
are the above-mentioned additives imparting electric conductivity
and in addition, fine particles of metal oxides,
fluoroalkoxysilane, surfactants (anionic, cationic, amphorytic and
nonionic surfactants) and the like.
[0396] Examples of the preferable anti-static agent to be added to
the undercoat layer are fine particles of metal oxides, concretely
antimony-doped tin oxide (ATO) and indium-containing tin oxide
(ITO) since the anti-static effect is high, is maintained for a
long period of time and is hardly affected by humid and since the
refractive index of the substrate can be adjusted because
transparency and refractive index of the anti-static agent are
high, thereby enabling the reflection reducing effect to be
enhanced. From the viewpoint of transparency, ATO is preferred, and
from the viewpoint of anti-static effect or electric conductivity,
ITO is preferred. Even in case where no anti-static effect is
required, a reflection reducing effect can be increased with those
additives since the refractive index can be adjusted easily.
[0397] Also since ATO and ITO easily scatter and absorb light, in
order not to prevent transmission of light, the thickness of the
undercoat layer is preferably sub-micron or so. In order to
decrease dependency of the reflection reducing effect on a
wavelength and to increase the reflection reducing effect
throughout the whole wavelength, the thickness of the undercoat
layer is preferably from 0.05 to 0.3 .mu.m though it depends on the
refractive index of the cured fluorine-containing prepolymer. An
optimum refractive index is preferably from 1.55 to 1.95 though it
also depends on the refractive index of the fluorine-containing
polymer.
[0398] In order to impart anti-static property to the cured
fluorine-containing prepolymer coating film, alkoxysilane
anti-static agents are preferred from the point that the refractive
index is hardly increased and those agents do not have an adverse
effect on the reflection reducing effect. Fluoroalkoxysilane is
further preferred since its action to increase the refractive index
is further smaller and in addition, an effect of improving surface
characteristics can be expected.
[0399] Also as a method entirely different from the above-mentioned
method of modifying a part of the film, there is a method of
forming a surfactant layer in a thickness not having an adverse
effect on the reflection reducing ability as mentioned in
JP8-142280A. When this method is applied to the present invention,
there is an effect of preventing adhesion of dust and enhancing
stain-proofing property. There is the same effect also in the case
of forming the hard coat layer.
[0400] The hard coat layer can be formed by the method of coating a
solution of alkoxysilane or polysilazane and then heating and
curing. Also a cured film obtained from an ultraviolet curable
acrylic coating or a cured film obtained by melamine-crosslinking
can be used.
[0401] Further the antireflection film of the present invention may
be provided on an undercoat layer formed by applying a coating
agent containing fine particles as a flattening agent, namely on a
substrate film (for example, TAC film and the like) subjected to
anti-glaring (AG) treatment. Thereby the antireflection film having
a low gloss and a low reflection can be obtained. Such a film, when
used for LCD and the like, is preferred since a further vivid image
can be obtained.
[0402] The antireflection film of the present invention has a high
fluorine content and a low surface contact angle and also possesses
water repelling property, non-tackiness and stain-proofing property
and therefore can be used as both of the antireflection layer and
stain-proofing layer.
[0403] Further in order to impart stain-proofing property to the
antireflection layer, a fluorine-containing polyether compound can
be added. In that case, the adding amount of the compound need be
decided in consideration of lowering of mechanical properties and
white turbidity due to phase separation from the
fluorine-containing polymer. When carboxyl group, blocked carboxyl
group, hydroxyl group, epoxy group, alkoxysilane group,
(meth)acryloyl group or .alpha.-fluoroacryloyl group is introduced
to an end of the compound, the compound is easily fixed in the
coating film (Experimental Examples 33, 34 and 35). Also there is
the same effect when the same polyether compound as above is coated
on a surface of a previously formed antireflection film (a coating
film before or after curing).
[0404] For forming a thin film of the curable fluorine-containing
polymer, there are a method of coating a dispersion of the curable
fluorine-containing polymer, drying and then baking if necessary
and a method of coating a solution (uniform solution) of the
polymer and then drying. Preferred is the coating of the solution
since a thin film is easily formed. In that case, as far as a
coating thickness can be controlled sufficiently, known coating
methods can be employed. For example, a roll coating method, micro
gravure coating method, gravure coating method, flow coating
method, bar coating method, spray coating method, die coating
method, spin coating method and dip coating method can be employed.
The optimum coating method is selected from them in consideration
of a balance of productivity, controllability of a coating
thickness, yield, etc. The antireflection film formed into a film
or sheet may be adhered to a substrate.
[0405] In the present invention, a silane compound may be added to
enhance adhesion of the antireflection film to the substrate. An
amount of the silane compound added to the coating film may be
several % by weight. Also treating of a substrate surface with a
silane compound has an effect on improvement of adhesion. In the
present invention, in any of the above cases, the silane compound
hardly increases the refractive index of the cured film and
therefore an influence thereof on the reflection reducing effect is
very small.
[0406] The present invention is then explained by means of
experimental examples, but is not limited to them.
PREPARATION EXAMPLE 1
[0407] (Synthesis of homopolymer of fluorine-containing allyl ether
having OH group)
[0408] A 100 ml four-necked glass flask equipped with a stirrer and
thermometer was charged with 20.4 g of
perfluoro-(1,1,9,9-tetrahydro-2,5--
bistrifluoromethyl-3,6-dioxanonenol): 60
[0409] and 21.2 g of a perfluorohexane solution of 8.0% by weight
of:
[0410] [HCF.sub.2CF.sub.2.paren close-st..sub.3COO.sub.2
[0411] and after the inside of the flask was sufficiently replaced
with nitrogen gas, stirring was carried out at 20.degree. C. for 24
hours in nitrogen gas stream and thereby a solid having a high
viscosity was produced.
[0412] The obtained solid was dissolved in diethyl ether and poured
into perfluorohexane, followed by separating and vacuum drying to
obtain 17.6 g of a transparent colorless polymer.
[0413] According to .sup.19F-NMR, .sup.1H-NMR and IR analyses, the
polymer was a fluorine-containing polymer consisting of the
structural unit of the above-mentioned fluorine-containing allyl
ether and having hydroxyl at an end of its side chain. The number
average molecular weight of the polymer was 9,000 according to the
GPC analysis using tetrahydrofuran (THF) as a solvent and the
weight average molecular weight thereof was 22,000.
EXPERIMENTAL EXAMPLE 1
[0414] (Synthesis of curable fluorine-containing polymer having
.alpha.-fluoroacryloyl group)
[0415] A 200 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 80 ml of
diethyl ether, 5.0 g of the fluorine-containing allyl ether
homopolymer having hydroxyl which was obtained in Preparation
Example 1 and 1.0 g of pyridine, followed by cooling to 5.degree.
C. or lower with ice.
[0416] Then a solution obtained by dissolving 1.0 g of
.alpha.-fluoroacrylic acid fluoride CH.sub.2.dbd.CFCOF in 20 ml of
diethyl ether was added thereto dropwise over about 30 minutes
while stirring in nitrogen gas stream.
[0417] After completion of the addition, the flask temperature was
raised to room temperature and the stirring was further continued
for 4.0 hours.
[0418] The ether solution after the reaction was put in the
dropping funnel, followed by washing with water, 2% hydrochloric
acid solution, 5% NaCl solution and water and then drying with
anhydrous magnesium sulfate. Then the ether solution was separated
by filtration.
[0419] According to .sup.19F-NMR analysis of the ether solution,
the obtained polymer was a copolymer comprising a
fluorine-containing allyl ether having 61
[0420] group and a fluorine-containing allyl ether having OH group
in a ratio of 40:60% by mole.
[0421] The ether solution was coated on a NaCl plate and formed
into a cast film at room temperature. According to IR analysis of
the cast film, an absorption of a carbon-carbon double bond was
observed at 1,661 cm.sup.-1, and an absorption of C.dbd.O group was
observed at 1,770 cm.sup.-1.
EXPERIMENTAL EXAMPLE 2
[0422] (Synthesis of curable fluorine-containing polymer having
.alpha.-fluoroacryloyl group)
[0423] A curable fluorine-containing polymer (ether solution) was
synthesized in the same manner as in Experimental Example 1 except
that 0.65 g of .alpha.-fluoroacrylic acid fluoride
CH.sub.2.dbd.CFCOF and 1.0 g of pyridine were used.
[0424] According to .sup.19F-NMR analysis, the polymer was a
copolymer comprising a fluorine-containing allyl ether having
62
[0425] group and a fluorine-containing allyl ether having OH group
in a ratio of 30:70% by mole.
[0426] According to IR analysis, an absorption of a carbon-carbon
double bond and an absorption of C.dbd.O group were observed at the
same positions, respectively as in Experimental Example 1.
EXPERIMENTAL EXAMPLE 3
[0427] (Synthesis of curable fluorine-containing polymer having
.alpha.-fluoroacryloyl group)
[0428] A curable fluorine-containing polymer (ether solution) was
synthesized in the same manner as in Experimental Example 1 except
that 0.35 g of .alpha.-fluoroacrylic acid fluoride
CH.sub.2.dbd.CFCOF and 0.3 g of pyridine were used.
[0429] According to .sup.19F-NMR analysis, the polymer was a
copolymer comprising a fluorine-containing allyl ether having
63
[0430] group and a fluorine-containing allyl ether having OH group
in a ratio of 15:85% by mole.
[0431] According to IR analysis, an absorption of a carbon-carbon
double bond and an absorption of C.dbd.O group were observed at the
same positions, respectively as in Experimental Example 1.
EXPERIMENTAL EXAMPLE 4
[0432] (1) Preparation of Fluorine-Containing Resin Composition for
Coating
[0433] After methyl ethyl ketone (MEK) was added to the
fluorine-containing polymer (ether solution) having
.alpha.-fluoroacryloyl group which was obtained in Experimental
Example 1, ether was distilled off with an evaporator to adjust a
concentration of the polymer to 8.0% by weight.
[0434] To 10 g of the obtained polymer solution was added, as an
active energy curing initiator, 1.7 g of a solution obtained by
dissolving 2-hydroxy-2-methyl propiophenone in MEK in a
concentration of 1% by weight.
[0435] (2) Production of Antireflection Film
[0436] The above-mentioned coating composition was coated on a
non-treated acryl plate at room temperature at 1,000 to 2,000 rpm
with a spin coater, followed by drying at 50.degree. C. for five
minutes. The number of revolutions of the spin coater was adjusted
so that a coating thickness after the drying became from 90 to 110
nm.
[0437] (Light Irradiation)
[0438] The coating film after the drying was irradiated with
ultraviolet light at an intensity of 3,000 mJ/cm.sup.2U using a
high pressure mercury lamp.
[0439] (3) Measurement of Refractive Index of Curable
Fluorine-Containing Polymer
[0440] The 8% MEK solution of the curable fluorine-containing
polymer (the polymer solution before adding the catalyst for curing
in (1) above) was coated on a PET film with an applicator so that a
coating thickness after the drying became about 100 .mu.m. After
drying at 50.degree. C. for ten minutes, the obtained cast film was
peeled from the PET film and a refractive index thereof was
measured using an Abbe's refractometer at 25.degree. C. with light
having a wavelength of 550 nm. The results are shown in Table
1.
[0441] (4) Measurement of Refractive Index of Cured Film
[0442] The coating composition prepared in (1) above was coated on
an aluminum foil with an applicator so that a coating thickness
became about 100 .mu.m, followed by drying at 50.degree. C. for ten
minutes. After the light irradiation was carried out in the same
manner as in (2) above, the aluminum foil was melted with diluted
hydrochloric acid to obtain a sample film. A refractive index of
the obtained cured film was measured in the same manner as in (3)
above.
[0443] (5) Measurement of Reflectance of One Side of Film
[0444] The acryl plate having the antireflection film which was
obtained in (2) above was set on a UV-VIS spectrophotometer
equipped with a 5.degree. regular reflection unit, and a
reflectance was measured with light having a wavelength of 550
nm.
[0445] (6) Evaluation of Physical Properties of Antireflection
Film
[0446] The following physical properties of the antireflection film
obtained in (2) above were evaluated.
[0447] {circle over (1)} Set to Touch
[0448] Tackiness of the film is evaluated by touching with a finger
according to JIS K4500.
[0449] The evaluation is made as follows.
[0450] .largecircle.: There is no tackiness.
[0451] x: There is tackiness.
[0452] {circle over (2)} Pencil Hardness
[0453] Measured according to JIS K5400.
[0454] {circle over (3)} Solvent Resistance
[0455] After the surface of the coating film is rubbed with a
cotton cloth impregnated with ethyl acetate, condition (dissolved
or peeled) of the surface is evaluated.
[0456] When there is no change, it is evaluated as .largecircle.,
and when there is dissolving or peeling, it is evaluated as x.
[0457] The evaluation is also carried out in the same manner as
above with respect to the case using acetone as a solvent.
[0458] {circle over (4)} Abrasion Resistance
[0459] A cotton cloth (BEMCOT (Registered trademark) M-3 available
from Asahi Chemical Co., Ltd.) is fitted to a rubbing tester, and
the antireflection film is rubbed by 100 rubbing cycles at a load
of 100 gf/cm.sup.2. Then the condition of the film is observed.
[0460] The evaluation is made as follows.
[0461] .largecircle.: There is no change.
[0462] .DELTA.: A flaw is found partly.
[0463] x: There is a portion where a film is peeled and a substrate
is seen.
EXPERIMENTAL EXAMPLES 5 to 6
[0464] Preparation of a coating composition, production of an
antireflection film and evaluation of a coating film were carried
out in the same manner as in Experimental Example 4 except that the
fluorine-containing polymers of Experimental Example 2
(Experimental Example 5) and Experimental Example 3 (Experimental
Example 6) were used instead of the fluorine-containing polymer
having .alpha.-fluoroacryloyl group which was obtained in
Experimental Example 1. The results are shown in Table 1.
EXPERIMENTAL EXAMPLE 7
[0465] An antireflection film was produced in the same manner as in
Experimental Example 4 except that light irradiation was not
conducted in producing the antireflection film, and evaluation of
physical properties was made. The results are shown in Table 1.
EXPERIMENTAL EXAMPLE 8
[0466] A reflectance of one side of a non-coated acryl plate was
measured. The results are shown in Table 1.
1 TABLE 1 Experimental Example 4 5 6 7 8 Substrate film Acryl Acryl
Acryl Acryl Acryl Curable fluorine-containing Exp. Ex. 1 Exp. Ex. 2
Exp. Ex. 3 Exp. Ex. 1 polymer Content of
--O(C.dbd.O)CF.dbd.CH.sub.2 40 30 15 40 group (% by mole) Solvent
MEK MEK MEK MEK Non-coated Concentration of polymer 8.0 8.0 8.0 8.0
(% by weight) Active energy curing agent 2-hydroxy-2- 2-hydroxy-2-
2-hydroxy-2- 2-hydroxy-2- methyl- methyl- methyl- methyl-
propiophenone propiophenone propiophenone propiophenone Proportion
to polymer 2.1 2.1 2.1 2.1 (% by weight) Amount of ultraviolet
3,000 3,000 3,000 Not irradiated irradiation (mJ/cm.sup.2)
Refractive index Before curing 1.362 1.359 1.356 -- Non-coated
After curing 1.366 1.364 1.361 -- Reflectance of one side of 1.3
1.2 1.0 -- 4.0 film (%) Set to touch .largecircle. .largecircle.
.largecircle. X Non-coated Pencil hardness 2H 2H H B Solvent
resistance .largecircle. .largecircle. .largecircle. X Abrasion
resistance .largecircle. .largecircle. .largecircle. X
EXPERIMENTAL EXAMPLES 9 to 12
[0467] (Determination of Curing Reactivity by IR Analysis)
[0468] (1) Preparation of Fluorine-Containing Resin Composition for
Coating
[0469] Respective coating compositions were prepared using the
curable fluorine-containing polymer obtained in Experimental
Example 1 by the same procedures as in Experimental Example 4 so
that the concentrations of the polymer and the amounts of active
energy curing initiator became those shown in Table 2.
[0470] (2) Production of Film for IR Analysis
[0471] The coating compositions prepared in (1) above were coated
on a PET film with an applicator so that a coating thickness after
drying became about 100 .mu.m, followed by drying at 50.degree. C.
for five minutes. Then the obtained coating films were peeled from
the PET film to obtain cast films.
[0472] (3) Measurement of Curing Reactivity by IR Analysis
[0473] According to IR analysis of the cast films, an absorption of
a carbon-carbon double bond in the polymer was observed at 1,661
cm.sup.-1.
[0474] Attention was directed to this absorption of the
carbon-carbon double bond, and a change in an intensity of
absorption after the light irradiation was measured. A ratio of
curing reaction was measured by the following equation. 1 ( 1 -
Peak height at 1 , 661 cm - 1 after light irradiation Peak height
at 1 , 661 cm - 1 before light irradiation ) .times. 100 %
[0475] The films were irradiated with ultraviolet light at room
temperature in irradiation amounts shown in Table 2 using a high
pressure mercury lamp. The amount of irradiation was changed and
the ratio of curing reaction represented by the above equation was
calculated. The results are shown in Table 2.
2 TABLE 2 Experimental Example 9 10 11 12 Curable
fluorine-containing Exp. Ex. 1 Exp. Ex. 1 Exp. Ex. 1 Exp. Ex. 1
polymer Content of --O(C.dbd.O)CF.dbd.CH.s- ub.2 group 40 40 40 40
(% by mole) Solvent MEK MEK MEK MEK Concentration of polymer 8 8 8
8 (% by weight) Active energy curing initiator 2-hydroxy-2-
2-hydroxy-2- 2-hydroxy-2- 2-hydroxy-2- methyl- methyl- methyl-
methyl- propiophenone propiophenone propiophenone propiophenone
Proportion to polymer 4.2 2.1 1.0 0.2 (% by weight) Ratio of curing
reaction (%) Amount of ultraviolet irradiation (mJ/cm.sup.2) 100
100 60 45 34 (disappeared) 500 -- 82 60 44 1,500 -- 100 74 55
(disappeared)
EXPERIMENTAL EXAMPLE 13
[0476] (Synthesis of Curable Fluorine-Containing Polymer Having
.alpha.-Fluoroacryloyl Group)
[0477] A curable fluorine-containing polymer (ether solution) was
synthesized in the same manner as in Experimental Example 1 except
that 2.0 g of .alpha.-fluoroacrylic acid fluoride
(CH.sub.2.dbd.CFCOF) and 2.0 g of pyridine were used.
[0478] According to .sup.19F-NMR analysis of the ether solution,
the polymer was a copolymer comprising a fluorine-containing allyl
ether having 64
[0479] group and a fluorine-containing allyl ether having OH group
in a ratio of 84:16% by mole.
[0480] According to IR analysis, an absorption of a carbon-carbon
double bond and an absorption of C.dbd.O group were observed at the
same positions, respectively as in Experimental Example 1.
EXPERIMENTAL EXAMPLES 14 to 16
[0481] (Determination of Curing Reactivity by IR Analysis)
[0482] (1) Preparation of Fluorine-Containing Resin Composition for
Coating
[0483] Respective coating compositions were prepared using the
curable fluorine-containing polymer obtained in Experimental
Example 13 by the same procedures as in Experimental Example 4 so
that the concentrations of the polymer and kinds and amounts of
active energy curing initiator became those shown in Table 3.
[0484] (2) Production of Film for IR Analysis
[0485] The films were produced in the same manner as in
Experimental Example 9.
[0486] (3) Measurement of Curing Reactivity by IR Analysis
[0487] A ratio of curing reaction when light irradiation was
carried out in a light irradiation amount of 1,500 mJ/cm.sup.2 was
calculated in the same manner as in Experimental Example 9. The
results are shown in Table 3.
EXPERIMENTAL EXAMPLE 17
[0488] A fluorine-containing resin composition for coating was
prepared by adding, as a curing agent, 65
[0489] to the coating composition obtained in Experimental Example
14 so that the amount thereof became 20% by weight based on the
polymer.
[0490] A film for IR analysis was produced using this resin
composition in the same manner as in Experimental Example 14, and a
curing reactivity was determined. The results are shown in Table
3.
3 TABLE 3 Experimental Example 14 15 16 17 Curable
fluorine-containing Exp. Ex. 13 Exp. Ex. 13 Exp. Ex. 13 Exp. Ex. 13
polymer Content of --O(C.dbd.O)CF.dbd.CH.sub.2 group 84 84 84 84 (%
by mole) Solvent MEK MEK MEK MEK Concentration of polymer 8 8 8 8
(% by weight) Active energy curing initiator 2-hydroxy-2-
2,2-dimethoxy- Benzophenone 2-hydroxy-2- methyl- 2-phenyl- methyl-
propiophenone acetophenone propiophenone Proportion to polymer 2.0
2.0 2.0 2.0 (% by weight) Curing agent -- -- -- Polyfunctional
acryl.sup.1) Proportion to polymer -- -- -- 20 (% by weight) Ratio
of curing reaction (%) 73.9 55.0 40.6 84.0 (at 1,500 mJ/cm.sup.2)
.sup.1)Polyfunctional acryl: CH.sub.2.dbd.CF(C.dbd.O)OCH.sub.2-
--(CF.sub.2).sub.6--CH.sub.2O(C.dbd.O)CF.dbd.CH.sub.2
PREPARATION EXAMPLE 2
[0491] (Synthesis of Homopolymer of Fluorine-Containing Allyl Ether
Having OH Group)
[0492] Synthesis of a polymer and refining of the obtained polymer
were carried out in the same manner as in Preparation Example 1
except that 20.0 g of
perfluoro-(1,1,9,9-tetrahydro-2,5-bistrifluoromethyl-3,6-dioxan-
onenol) and 10.0 g of a perfluorohexane solution of 8.0% by weight
of:
[0493] [HCF.sub.2CF.sub.2.paren close-st..sub.3COO.sub.2
[0494] were used. Thus 18.2 g of a transparent colorless polymer
was obtained.
[0495] According to .sup.19F-NMR, .sup.1H-NMR and IR analyses, the
obtained polymer was a fluorine-containing polymer consisting of
the structural unit of the above-mentioned fluorine-containing
allyl ether and having hydroxyl at an end of its side chain. The
number average molecular weight of the polymer was 30,000 according
to the GPC analysis using tetrahydrofuran (THF) as a solvent and
the weight average molecular weight thereof was 59,000.
PREPARATION EXAMPLE 3
[0496] (Synthesis of Copolymer Comprising Fluorine-Containing Allyl
Ether Having OH Group and Vinylidene Fluoride)
[0497] A 300 ml stainless steel autoclave equipped with a valve,
pressure gauge and thermometer was charged with 34.2 g of
perfluoro-(1,1,9,9-tetra-
hydro-2,5-bistrifluoromethyl-3,6-dioxanonenol), 200 g of
CH.sub.3CCl.sub.2F (HCFC-141b) and 0.16 g of methanol solution of
50% by weight of dinormalpropyl peroxy carbonate (NPP). While
cooling with dry ice/methanol solution, the inside of a system was
sufficiently replaced with nitrogen gas. Then 5.8 g of vinylidene
fluoride (VdF) was introduced through the valve, followed by
reaction while shaking at 40.degree. C. With the advance of the
reaction, 12 hours after starting of the reaction, a gauge pressure
inside the system lowered from 4.4 MPaG (4.5 kgf/cm.sup.2G) before
the reaction to 0.98 MPaG (1.0 kgf/cm.sup.2G).
[0498] At that time, un-reacted monomer was released and a
precipitated solid was removed and dissolved in acetone, followed
by re-precipitation with a solvent mixture of hexane and toluene
(50/50) to separate a copolymer. The copolymer was vacuum-dried
until a constant weight was reached. Thereby 31.2 g of a copolymer
was obtained.
[0499] The components of the copolymer were VdF and the
fluorine-containing allyl ether having OH group in a ratio of
38:62% by mole according to .sup.1H-NMR and .sup.19F-NMR analyses.
The number average molecular weight of the copolymer was 12,000
according to the GPC analysis using THF as a solvent and the weight
average molecular weight thereof was 18,000.
EXPERIMENTAL EXAMPLE 18
[0500] (Synthesis of Fluorine-Containing Active Energy Curing
Initiator)
[0501] A 200 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 2.0 g of
2-hydroxy-2-methyl propiophenone, 1.0 g of pyridine and 20 g of a
mixture (HCFC-225) of CF.sub.3CF.sub.2CHCl/CClF.sub.2CF.sub.2CHClF
and was cooled to 5.degree. C. or lower with ice.
[0502] Thereto was added dropwise 2.5 g of: 66
[0503] over one hour with stirring in nitrogen gas stream. After
completion of the addition, the stirring was further continued for
4.0 hours.
[0504] After the reaction, the ether solution was put in the
dropping funnel and washed with 2% hydrochloric acid solution and
5% NaCl solution, followed by separation of an organic layer,
drying with anhydrous magnesium sulfate and distillation to isolate
2.6 g of a product (yield: 62%).
[0505] According to .sup.1H-NMR, .sup.19F-NMR and IR analyses, the
product was: 67
EXPERIMENTAL EXAMPLE 19
[0506] (Synthesis of Curable Fluorine-Containing Polymer Having
.alpha.-Fluoroacryloyl Group)
[0507] A 200 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 40 ml of
methyl ethyl ketone (MEK), 5.0 g of the fluorine-containing allyl
ether homopolymer having hydroxyl which was obtained in Preparation
Example 2 and 2.0 g of pyridine, and was cooled to 5.degree. C. or
lower with ice.
[0508] Thereto was added dropwise 1.2 g of .alpha.-fluoroacrylic
acid fluoride over about 30 minutes with stirring in nitrogen gas
stream. After completion of the addition, the flask temperature was
raised to room temperature and the stirring was further continued
for 4.0 hours.
[0509] After the reaction, the MEK solution was put in the dropping
funnel and washed with water, 2% hydrochloric acid solution, 5%
NaCl solution and water, followed by separation of an organic layer
and drying with anhydrous magnesium sulfate. A concentration of the
polymer after filtrating was 10.7% by weight.
[0510] According to .sup.19F-NMR analysis of the MEK solution, the
obtained polymer was a copolymer comprising a fluorine-containing
allyl ether having 68
[0511] group and a fluorine-containing allyl ether having OH group
in a ratio of 89:11% by mole.
[0512] According to IR analysis which was carried out in the same
manner as in Experimental Example 1, an absorption of a
carbon-carbon double bond and an absorption of C.dbd.O group were
observed at 1,660 cm.sup.-1 and 1,770 cm.sup.-1, respectively.
EXPERIMENTAL EXAMPLE 20
[0513] (Synthesis of Curable Fluorine-Containing Polymer Having
.alpha.-Fluoroacryloyl Group)
[0514] A curable fluorine-containing polymer (MEK solution) was
synthesized in the same manner as in Experimental Example 19 except
that 5.0 g of the copolymer of the fluorine-containing allyl ether
having OH group and VdF which was obtained in Preparation Example
3, 1.1 g of pyridine and 1.0 g of .alpha.-fluoroacrylic acid
fluoride were used. A concentration of the polymer was 9.9% by
weight.
[0515] According to .sup.19F-NMR analysis, the polymer was a
copolymer comprising a fluorine-containing allyl ether having
69
[0516] group, a fluorine-containing allyl ether having OH group and
VdF in a ratio of 48:14:38% by mole.
EXPERIMENTAL EXAMPLE 21
[0517] (1) Preparation of Fluorine-Containing Resin Composition for
Coating
[0518] MEK was added to the curable fluorine-containing polymer
(MEK solution) obtained in Experimental Example 19 to adjust the
concentration of the polymer to 8% by weight.
[0519] To the MEK solution of the curable fluorine-containing
polymer was added 2-hydroxy-2-methyl propiophenone as the active
energy curing initiator so that its amount became 2.0% by weight
based on the polymer. However the solution became turbid in white
and the both could not be compatible with each other.
[0520] Therefore the fluorine-containing active energy curing
initiator obtained in Experimental Example 18 was added instead of
2-hydroxy-2-methyl propiophenone so that its amount became 3.6% by
weight based on the polymer. As a result, a transparent colorless
solution was obtained and the both were compatible with each
other.
[0521] (2) Evaluation of Coating Composition
[0522] The coating composition containing the fluorine-containing
active energy curing initiator was evaluated in the same manner as
in (2) to (6) of Experimental Example 4 (in (2), irradiation of
light was carried out at 1,500 mJ/cm.sup.2), and a ratio of curing
reaction when irradiated with light of 1,500 mJ/cm.sup.2 was
measured in the same manner as in Experimental Example 10. The
results are shown in Table 4.
EXPERIMENTAL EXAMPLE 22
[0523] (1) Preparation of Fluorine-Containing Resin Composition for
Coating
[0524] MEK was added to the curable fluorine-containing polymer
(MEK solution) obtained in Experimental Example 20 to adjust the
concentration of the polymer to 8% by weight.
[0525] To the MEK solution of the curable fluorine-containing
polymer was added 2-hydroxy-2-methyl propiophenone as the active
energy curing initiator so that its amount became 6.7% by weight
based on the polymer. As a result, a transparent colorless solution
was obtained and the both were compatible with each other.
[0526] (2) Evaluation of Coating Composition
[0527] The obtained coating composition was evaluated in the same
manner as in Experimental Example 21. The results are shown in
Table 4.
4TABLE 4 Experimental Example 21 22 Substrate film Acryl Acryl
Curable fluorine-containing polymer Exp. Ex. 19 Exp. Ex. 20 Content
of --O(C.dbd.O)CF.dbd.CH.sub.2 group 89 48 (% by mole) Solvent MEK
MEK Concentration of polymer 8 8 (% by weight) Active energy curing
agent Fluorine- 2-hydroxy- containing initiator of 2-methyl- Exp.
Ex. 18.sup.2 2-methyl- pro- piophenone Proportion to polymer 3.6
6.7 (% by weight) Amount of ultraviolet irradiation 1,500 1,500
(mJ/cm.sup.2) Ratio of curing reaction (%) 88.7 75.7 (at 1,500
mJ/cm.sup.2) Refractive index Before curing 1.368 1.369 After
curing 1.375 1.377 Reflectance of one side of film (%) 1.40 1.42
Set to touch .largecircle. .largecircle. Pencil hardness 2H 2H
Solvent resistance .largecircle. .largecircle. Abrasion resistance
.largecircle. .largecircle. .sup.270
PREPARATION EXAMPLE 4
[0528] (Synthesis of Homopolymer of Fluorine-Containing Allyl Ether
Having OH Group)
[0529] A 100 ml four-necked glass flask equipped with a stirrer and
thermometer was charged with 20.8 g of
perfluoro-(1,1,9,9-tetrahydro-2,5--
bistrifluoromethyl-3,6-dioxanonenol) and 2.2 g of a perfluorohexane
solution of 8.0% by weight of:
[0530] [HCF.sub.2CF.sub.2.paren close-st..sub.3 COO.sub.2
[0531] and after the inside of the flask was sufficiently replaced
with nitrogen gas, stirring was carried out at 20.degree. C. for 24
hours in nitrogen gas stream and a solid having a high viscosity
was produced.
[0532] The obtained solid was dissolved in diethyl ether and poured
into perfluorohexane, followed by separating and vacuum drying to
obtain 19.2 g of a transparent colorless polymer.
[0533] According to .sup.19F-NMR, .sup.1H-NMR and IR analyses, the
polymer was a fluorine-containing polymer consisting of the
structural unit of the above-mentioned fluorine-containing allyl
ether and having hydroxyl at an end of its side chain. The number
average molecular weight of the polymer was 72,000 according to the
GPC analysis using tetrahydrofuran (THF) as a solvent and the
weight average molecular weight thereof was 118,000.
EXPERIMENTAL EXAMPLE 23
[0534] (Synthesis of Curable Fluorine-Containing Polymer Having
.alpha.-Fluoroacryloyl Group)
[0535] A 200 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 50 ml of
methyl ethyl ketone (MEK), 5.0 g of the fluorine-containing allyl
ether homopolymer having hydroxyl which was obtained in Preparation
Example 4 and 2.5 g of pyridine, and was cooled to 5.degree. C. or
lower with ice.
[0536] Then a solution obtained by dissolving 2.5 g of
.alpha.-fluoroacrylic acid fluoride CH.sub.2.dbd.CFCOF in 10 ml of
MEK was added thereto dropwise over about ten minutes with stirring
in nitrogen gas stream.
[0537] After completion of the addition, the flask temperature was
raised to room temperature and the stirring was further continued
for 2.0 hours.
[0538] After the reaction, the MEK solution was put in the dropping
funnel and washed with water, 2% hydrochloric acid solution, 5%
NaCl solution and water, followed by drying with anhydrous
magnesium sulfate and separating the solution by filtrating to
obtain the MEK solution. A concentration of the polymer was 13% by
weight.
[0539] According to .sup.19F-NMR analysis of the MEK solution, the
polymer was a copolymer comprising a fluorine-containing allyl
ether having --OCOCF.dbd.CH.sub.2 group and a fluorine-containing
allyl ether having OH group in a ratio of 70:30% by mole.
[0540] The solution was coated on a NaCl plate and formed into a
cast film at room temperature. According to IR analysis of the cast
film, an absorption of a carbon-carbon double bond and an
absorption of C.dbd.O group were observed at 1,661 cm.sup.-1 and
1,770 cm.sup.-1, respectively.
EXPERIMENTAL EXAMPLE 24
[0541] (1) Preparation of Fluorine-Containing Resin Composition for
Coating
[0542] MEK was added to the solution of fluorine-containing polymer
having .alpha.-fluoroacryloyl group which was obtained in
Experimental Example 23 to dilute the solution and adjust a
concentration of the polymer to 5.0% by weight.
[0543] To 10 g of the obtained polymer solution was added, as an
active energy curing initiator, 1.2 g of a solution obtained by
dissolving 2-hydroxy-2-methyl propiophenone in MEK in a
concentration of 1% by weight. Thus a uniform solution was
obtained.
[0544] (2) Production of Antireflection Film
[0545] The above-mentioned coating composition was coated on a
non-treated acryl plate at room temperature at 1,000 to 2,000 rpm
with a spin coater, followed by drying at 50.degree. C. for five
minutes. The number of revolutions of the spin coater was adjusted
so that a coating thickness after the drying became from 90 to 110
nm.
[0546] (Light Irradiation)
[0547] The coating film after the drying was irradiated with
ultraviolet light at room temperature at an intensity of 1,500
mJ/cm.sup.2U using a high pressure mercury lamp.
[0548] (3) Measurement of Refractive Index of Curable
Fluorine-Containing Polymer
[0549] The solution of fluorine-containing polymer having
.alpha.-fluoroacryloyl group which was obtained in Experimental
Example 23 was concentrated to 50% and coated on a PET film with an
applicator so that a coating thickness after the drying became
about 100 .mu.m. After drying at 50.degree. C. for ten minutes, the
obtained cast film was peeled from the PET film and a refractive
index thereof was measured using an Abbe's refractometer at
25.degree. C. with light having a wavelength of 550 nm. The results
are shown in Table 5.
[0550] (4) Measurement of Refractive Index of Cured Film
[0551] The solution of fluorine-containing polymer having
.alpha.-fluoroacryloyl group which was obtained in Experimental
Example 23 was concentrated to 50%, and to 2 g of the solution was
added 0.01 g of 2-hydroxy-2-methyl propiophenone as the active
energy curing initiator. The obtained solution was coated on an
aluminum foil with an applicator so that a coating thickness after
drying became about 100 .mu.m, followed by drying at 50.degree. C.
for ten minutes. After carrying out the light irradiation in the
same manner as in (2) above, the aluminum foil was melted with
diluted hydrochloric acid to obtain a sample film. A refractive
index of the obtained cured film was measured in the same manner as
in (3) above. The results are shown in Table 5.
[0552] (5) Measurement of Reflectance of One Side of Film
[0553] The acryl plate having the antireflection film which was
obtained in (2) above was set on a visible ultraviolet spectroscope
equipped with a 5.degree. regular reflection unit, and a
reflectance was measured with light having a wavelength of 550 nm.
The results are shown in Table 5.
[0554] (6) Evaluation of Physical Properties of Antireflection
Film
[0555] The following physical properties of the surface of the
antireflection film obtained in (2) above were evaluated. The
results are shown in Table 5.
[0556] {circle over (1)} Pencil Hardness
[0557] Measured according to JIS K5400.
[0558] {circle over (2)} Solvent Resistance
[0559] After the surface of the coating film is rubbed with a
cotton cloth impregnated with ethyl acetate, condition (dissolved
or peeled) of the film surface is evaluated.
[0560] When there is no change, it is evaluated as .largecircle.,
and when there is dissolution or peeling, it is evaluated as x.
[0561] The evaluation is also carried out in the same manner as
above with respect to the case using acetone as a solvent.
[0562] {circle over (3)} Abrasion Resistance
[0563] A cotton cloth (BEMCOT (Registered trademark) M-3 available
from Asahi Chemical Co., Ltd.) is fitted to a rubbing tester, and
the antireflection film is rubbed by 100 rubbing cycles at a load
of 100 gf/cm.sup.2 to observe conditions of the film.
[0564] The evaluation is made as follows.
[0565] .largecircle.: There is no change.
[0566] .DELTA.: A flaw is found partly.
[0567] x: There is a portion where a film is peeled and a substrate
is seen.
[0568] {circle over (4)} Scratch Resistance
[0569] After the surface of the coating film is rubbed with steel
wool #0000, condition of the surface is evaluated.
[0570] The evaluation is made as follows.
[0571] .largecircle.: There is no change.
[0572] .DELTA.: A flaw is found at several parts.
[0573] x: There are many large flaws or the film is peeled and a
substrate is seen.
EXPERIMENTAL EXAMPLES 25 to 27
[0574] To the coating composition obtained in (1) of Experimental
Example 24 was added, as a curing agent, 71
[0575] so that its amount became 10% by weight (Experimental
Example 25), 30% by weight (Experimental Example 26) and 50% by
weight (Experimental Example 27) based on the polymer.
Antireflection films were produced in the same manner as in (2) of
Experimental Example 24 using the respective coating compositions,
and physical properties of the antireflection films were evaluated
in the same manner as in (4) Measurement of refractive index of
cured film, (5) Measurement of reflectance of one side of film and
(6) Evaluation of physical properties of antireflection film. The
results are shown in Table 5.
EXPERIMENTAL EXAMPLE 28
[0576] (1) Preparation of Fluorine-Containing Resin Composition for
Coating
[0577] To 0.5 g of the curing agent: 72
[0578] used in Experimental Example 25 was added 10 g of MEK to
dissolve the curing agent, and thereto was added 1.2 g of a
solution obtained by dissolving 2-hydroxy-2-methyl propiophenone as
the active energy curing initiator in a concentration of 1% by
weight in MEK to obtain a uniform solution. An antireflection film
was produced in the same manner as in (2) of Experimental Example
24 using the obtained coating composition, and physical properties
of the antireflection film were evaluated in the same manner as in
(4) Measurement of refractive index of cured film, (5) Measurement
of reflectance of one side of film and (6) Evaluation of physical
properties of antireflection film. The results are shown in Table
5.
EXPERIMENTAL EXAMPLE 29
[0579] A fluorine-containing resin composition for coating was
prepared in the same manner as in Experimental Example 17 except
that 73
[0580] was added as a curing agent in an amount of 30% by weight
based on the polymer. Thereto was added MEK to obtain 5% by weight
solution in MEK. An antireflection film was produced in the same
manner as in (2) of Experimental Example 24 using the obtained
coating composition, and physical properties of the antireflection
film were evaluated in the same manner as in (4) Measurement of
refractive index of cured film, (5) Measurement of reflectance of
one side of film and (6) Evaluation of physical properties of
antireflection film. The results are shown in Table 5.
EXPERIMENTAL EXAMPLE 30
[0581] (Synthesis of Curable Fluorine-Containing Polymer Having
.alpha.-Fluoroacryloyl Group)
[0582] A 200 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 50 ml of
MEK, 5.0 g of the copolymer comprising a fluorine-containing allyl
ether having OH group and VdF and obtained in Preparation Example 3
and 2.2 g of pyridine, and was cooled to 5.degree. C. or lower with
ice.
[0583] Then a solution obtained by dissolving 2.0 g of
.alpha.-fluoroacrylic acid fluoride CH.sub.2.dbd.CFCOF in 10 ml of
MEK was added thereto dropwise over about ten minutes with stirring
in nitrogen gas stream.
[0584] After completion of the addition, the flask temperature was
raised to room temperature and the stirring was further continued
for 3.0 hours.
[0585] After the reaction, the MEK solution was put in the dropping
funnel and washed with water, 2% hydrochloric acid solution, 5%
NaCl solution and water, followed by drying with anhydrous
magnesium sulfate and separating the MEK solution by filtrating. A
concentration of the polymer was 13.0% by weight.
[0586] According to .sup.19F-NMR analysis of the MEK solution, the
polymer was a copolymer comprising a fluorine-containing allyl
ether having --OCOCF.dbd.CH.sub.2 group and VdF in a ratio of
62:38% by mole.
[0587] The solution was coated on a NaCl plate and formed into a
cast film at room temperature. According to IR analysis of the cast
film, an absorption of a carbon-carbon double bond and an
absorption of C.dbd.O group were observed at 1,661 cm.sup.-1 and
1,770 cm.sup.-1, respectively.
EXPERIMENTAL EXAMPLE 31
[0588] (1) Preparation of coating composition, (2) Production of
antireflection film and evaluation of coating film were carried out
in the same manner as in Experimental Example 24 except that the
fluorine-containing polymer obtained in Experimental Example 30 was
used instead of the fluorine-containing polymer having
.alpha.-fluoroacryloyl group and obtained in Experimental Example
23 and the fluorine-containing energy curing initiator obtained in
Experimental Example 18 was used as the active energy curing
initiator instead of 2-hydroxy-2-methyl propiophenone. The results
are shown in Table 5.
EXPERIMENTAL EXAMPLE 32
[0589] To the coating composition obtained in (1) of Experimental
Example 31 was added, as a curing agent, 74
[0590] so that its amount became 10% by weight based on the polymer
to obtain a composition for coating. An antireflection film was
produced in the same manner as in (2) of Experimental Example 24
using the obtained coating composition, and (4) Measurement of
refractive index of cured film, (5) Measurement of reflectance of
one side of film and (6) Evaluation of physical properties of
antireflection film were carried out in the same manner. The
results are shown in Table 5.
5 TABLE 5 Experimental Example 24 25 26 27 28 29 31 32 Substrate
film Acryl Acryl Acryl Acryl Acryl Acryl Acryl Acryl Curable Exp.
Ex. 23 Exp. Ex. 23 Exp. Ex. 23 Exp. Ex. 23 Exp. Ex. 17 Exp. Ex. 30
Exp. fluorine- Ex. 30 containing polymer Content of 70 70 70 70 84
62 62 --O(C.dbd.O)CF.dbd.CH.sub.2 group (% by mole) Crosslinking
Tetra- Tetrafunctional Tetrafunctional Tetrafunctional Only
Bifunctional Tetrafunctional Tetra- agent functional acryl.sup.1)
acryl.sup.1) acryl.sup.1) tetrafunctional acryl.sup.3) acryl.sup.1)
functional acryl.sup.1) acryl.sup.1) acryl.sup.1) Adding amount 0
10 30 50 30 0 10 (proportion to polymer (% by weight)) Active
energy 2-hydroxy-2- 2-hydroxy-2- 2-hydroxy-2- 2-hydroxy-2-
2-hydroxy-2- 2-hydroxy-2- Fluorine- Fluorine- curing agent methyl-
methyl- methyl- methyl- methyl- methyl- containing containing pro-
propiophenone propiophenone propiophenone propiophenone
propiophenone initiator.sup.2) initiator.sup.2) piophenone
Proportion 2 2 2 2 2 2 5 5 to polymer (% by weight) Amount of 1,500
1,500 1,500 1,500 1,500 1,500 1,500 1,500 ultraviolet irradiation
(mJ/cm.sup.2) Refractive index Before curing 1.366 -- -- -- -- --
1.370 -- After curing 1.374 1.381 1.395 1.432 1.465 1.390 1.381
1.384 Reflectance of 1.4 1.5 1.7 2% 3.0 1.6 1.5 1.5 one side of
film (%) Pencil hardness 2H 3H 4H 4H 5H 3H 3H 4H Solvent
.largecircle. .largecircle. .largecircle. .largecircle.
.largecircle. .largecircle. .largecircle. .largecircle. resistance
Abrasion .largecircle. .largecircle. .largecircle. .largecircle.
.largecircle. .largecircle. .largecircle. .largecircle. resistance
Scratch X .DELTA. .largecircle. .largecircle. .largecircle. .DELTA.
.DELTA. .largecircle. resistance
[0591] 1) Crosslinking Agent (Tetrafunctional) 75
[0592] 2) Fluorine-Containing Energy Curing Initiator 76
[0593] 3) Crosslinking Agent (Bifunctional) 77
EXPERIMENTAL EXAMPLE 33
[0594] (Synthesis of Perfluoropolyether .alpha.-Fluoroacrylate)
[0595] A 500 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 18 g of a
perfluoropolyether alcohol:
[0596]
CF.sub.3CF.sub.2CF.sub.2O(CF.sub.2CF.sub.2CF.sub.2O).sub.nCF.sub.2C-
F.sub.2CH.sub.2OH (n.apprxeq.20)
[0597] having a linear chain and an average molecular weight of
3,800, 1.0 g of pyridine and 125 g of
1,1,1,3,3,3-hexafluoromethaxylene, and was cooled to 5.degree. C.
or lower with ice.
[0598] Thereto was added dropwise a solution obtained by dissolving
0.84 g of .alpha.-fluoroacrylic acid fluoride CH.sub.2.dbd.CFCOF in
5 ml of 1,1,1,3,3,3-hexafluoromethaxylene over about ten minutes
with stirring in nitrogen gas stream.
[0599] After completion of the addition, the flask temperature was
raised to room temperature and the stirring was further continued
for four hours.
[0600] After the reaction, the ether solution was put in the
dropping funnel and washed with water, 2% hydrochloric acid
solution, 5% NaCl solution and water, followed by drying with
anhydrous magnesium sulfate and separating the solution by
filtrating. After distilling off the solvent from the filtrate with
an evaporator, the solution was dried for six hours in an evacuated
state while heating to 70.degree. C. and thus a transparent
colorless liquid having a high viscosity was obtained.
[0601] According to .sup.1H-NMR, .sup.19F-NMR and IR analyses, the
obtained product was 78
EXPERIMENTAL EXAMPLES 34 and 35
[0602] (Improvement of Surface Physical Properties with Compound
Having Perfluoropolyether Group (PFPE))
[0603] (1) Preparation of Fluorine-Containing Resin Composition for
Coating
[0604] The MEK solutions of fluorine-containing polymer having
.alpha.-fluoroacryloyl group which were obtained in Experimental
Example 23 (Experimental Example 34) and Experimental Example 30
(Experimental Example 35) were concentrated to adjust a
concentration thereof to 50% by weight, respectively. Then to 2 g
of the concentrated MEK solution were added 3 g of a
CF.sub.3CF.sub.2CHCl/CClF.sub.2CF.sub.2CHClF mixture (HCFC-225), 4
g of MIBK and 6 g of ClCF.sub.2CClFCF.sub.2CCl.sub.2F (CFC-316).
Further thereto was added 1.0 g of a solution obtained by
dissolving the perfluoropolyether a-fluoroacrylate obtained in
Experimental Example 33 in HCFC-225 in a concentration of 1.0% by
weight.
[0605] To the obtained polymer solution was added, as an active
energy curing initiator, 1 g of a solution obtained by dissolving a
fluorine-containing energy curing initiator in HCFC-225 in a
concentration of 10% by weight, and thus uniform solutions were
obtained.
[0606] (2) Production of Antireflection Film
[0607] The coating composition obtained above was coated on a
non-treated acryl plate at room temperature at 2,000 to 5,000 rpm
with a spin coater, followed by drying at 50.degree. C. for five
minutes. In that case, the number of revolutions of the spin coater
was adjusted so that a coating thickness after the drying became
from 90 to 110 nm.
[0608] (Light Irradiation)
[0609] The coating film after the drying was irradiated with
ultraviolet light at room temperature at an intensity of
irradiation of 1,500 mJ/cm.sup.2U using a high pressure mercury
lamp.
[0610] (3) Measurement of Reflectance of One Side of Film
[0611] The acryl plate having the antireflection film which was
obtained in (2) above was set on a visible ultraviolet spectroscope
equipped with a 5.degree. regular reflection unit, and a
reflectance was measured with light having a wavelength of 550 nm.
The results are shown in Table 6.
[0612] (4) Evaluation of Physical Properties of Antireflection
Film
[0613] The following physical properties of the surface of the
antireflection film obtained in (2) above were evaluated. The
results are shown in Table 6.
[0614] {circle over (1)} Pencil Hardness
[0615] Measured according to JIS K5400.
[0616] {circle over (2)} Contact Angle
[0617] Contact angles of pure water and n-hexadecane are measured
with a contact angle meter.
EXPERIMENTAL EXAMPLES 36 and 37
[0618] With respect to the antireflection films after the light
irradiation which were obtained in (2) of Experimental Example 24
(Experimental Example 36) and (2) of Experimental Example 31
(Experimental Example 37), a contact angle was measured in the same
manner as in (4) of Experimental Example 34. The results are shown
in Table 6.
PREPARATION EXAMPLE 5
[0619] (Synthesis of Fluorine-Containing Allyl Ether Homopolymer
Having OH Group (and Having Long Side Chain))
[0620] A 100 ml four-necked glass flask equipped with a stirrer and
thermometer was charged with 10.0 g of
CH.sub.2.dbd.CFCF.sub.2(OCF(CF.sub-
.3)CF.sub.2).sub.3OCF(CF.sub.3)CH.sub.2OH and 6.2 g of a
perfluorohexane solution of 8.0% by weight of:
[0621] [HCF.sub.2CF.sub.2.paren close-st..sub.3COO.sub.2
[0622] and after the inside of the flask was sufficiently replaced
with nitrogen gas, stirring was carried out at 20.degree. C. for 15
hours in nitrogen gas stream and a solid having a high viscosity
was produced.
[0623] The obtained solid was dissolved in diethyl ether and poured
into perfluorohexane, followed by separating and vacuum drying to
obtain 7.3 g of a transparent colorless polymer.
[0624] According to .sup.19F-NMR, .sup.1H-NMR and IR analyses, the
polymer was a fluorine-containing polymer consisting of the
structural unit of the above-mentioned fluorine-containing allyl
ether and having hydroxyl at an end of its side chain. The number
average molecular weight of the polymer was 24,000 according to the
GPC analysis using tetrahydrofuran (THF) as a solvent and the
weight average molecular weight thereof was 79,000.
EXPERIMENTAL EXAMPLE 38
[0625] (Synthesis of Curable Fluorine-Containing Polymer Having
.alpha.-Fluoroacryloyl Group (and Having Long Side Chain))
[0626] A 200 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 50 ml of
methyl ethyl ketone, 3.0 g of the fluorine-containing allyl ether
homopolymer having hydroxyl which was obtained in Preparation
Example 5 and 0.4 g of pyridine, followed by cooling to 5.degree.
C. or lower with ice.
[0627] Then a solution obtained by dissolving 0.55 g of
.alpha.-fluoroacrylic acid fluoride CH.sub.2.dbd.CFCOF in 10 ml of
methyl ethyl ketone was added thereto dropwise over about 10
minutes while stirring in nitrogen gas stream.
[0628] After completion of the addition, the flask temperature was
raised to room temperature and the stirring was further continued
for 2.0 hours.
[0629] The ether solution after the reaction was put in the
dropping funnel, followed by washing with water, 2% hydrochloric
acid solution, 5% NaCl solution and water and then drying with
anhydrous magnesium sulfate. Then the methyl ethyl ketone solution
was separated by filtration.
[0630] According to .sup.19F-NMR analysis of the methyl ethyl
ketone solution, the polymer was a copolymer comprising a
fluorine-containing allyl ether having --OCOCF.dbd.CH.sub.2 group
and a fluorine-containing allyl ether having OH group in a ratio of
54:46% by mole.
[0631] According to IR analysis, an absorption of a carbon-carbon
double bond and an absorption of C.dbd.O group were observed at the
same positions, respectively as in Experimental Example 23.
EXPERIMENTAL EXAMPLE 39
[0632] An antireflection film was produced in the same manner as in
(1) and (2) of Experimental Example 24 except that the
fluorine-containing polymer of Experimental Example 38 was used
instead of the fluorine-containing polymer having
.alpha.-fluoroacryloyl group and obtained in Experimental Example
23. Physical properties of the antireflection film were evaluated
in the same manner as in (3) and (4) of Experimental Example 34.
The results are shown in Table 6.
PREPARATION EXAMPLE 6
[0633] (Synthesis of Copolymer Comprising Fluorine-Containing Allyl
Ether Having OH Group and Fluorine-Containing Allyl Ether Having
Methyl Ester Structure at an End Thereof
[0634] A 100 ml four-necked glass flask equipped with a stirrer and
thermometer was charged with 9.6 g of
perfluoro-(1,1,9,9-tetrahydro-2,5-b-
istrifluoromethyl-3,6-dioxanonenol) and 9.6 g of
CH.sub.2.dbd.CFCF.sub.2OC-
F(CF.sub.3)CF.sub.2OCF(CF.sub.3)COOCH.sub.3, followed by stirring
sufficiently. Then thereto was added 2.0 g of a perfluorohexane
solution of 8.0% by weight of:
[0635] [HCF.sub.2CF.sub.2.paren close-st..sub.3COO.sub.2
[0636] and after the inside of the flask was sufficiently replaced
with nitrogen gas, stirring was carried out at 20.degree. C. for 20
hours in nitrogen gas stream and a solid having a high viscosity
was produced.
[0637] The obtained solid was dissolved in acetone and poured into
a HCFC-225/n-hexane=1/1 solution, followed by separating and vacuum
drying to obtain 15.5 g of a transparent colorless polymer.
[0638] According to .sup.19F-NMR, .sup.1H-NMR and IR analyses, the
product was a copolymer comprising the above-mentioned
fluorine-containing allyl ether having hydroxyl and
fluorine-containing allyl ether having a methyl ester structure at
an end thereof in a ratio of 42:58% by mole. The number average
molecular weight of the polymer was 72,000 according to the GPC
analysis using tetrahydrofuran (THF) as a solvent and the weight
average molecular weight thereof was 117,000.
EXPERIMENTAL EXAMPLE 40
[0639] (Synthesis of Curable Fluorine-Containing Polymer Having
.alpha.-Fluoroacryloyl Group)
[0640] A 200 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 50 ml of
methyl ethyl ketone, 3.0 g of the fluorine-containing allyl ether
copolymer having hydroxyl which was obtained in Preparation Example
6 and 0.6 g of pyridine. Thereto was added dropwise a solution
obtained by dissolving 1.0 g of .alpha.-fluoroacrylic acid fluoride
CH.sub.2.dbd.CFCOF in 10 ml of MEK in the same manner as in
Experimental Example 23. Thus a curable fluorine-containing polymer
(MEK solution) was synthesized.
[0641] According to .sup.19F-NMR analysis, the polymer was a
copolymer comprising a fluorine-containing allyl ether having
--OCOCF.dbd.CH.sub.2 group, a fluorine-containing allyl ether
having OH group and a fluorine-containing allyl ether having a
methyl ester structure at an end thereof in a ratio of 38:4:58% by
mole.
[0642] According to IR analysis, an absorption of a carbon-carbon
double bond and an absorption of C.dbd.O group were observed at the
same positions, respectively as in Experimental Example 23.
EXPERIMENTAL EXAMPLE 41
[0643] An antireflection film was produced in the same manner as in
(1) and (2) of Experimental Example 31 except that the
fluorine-containing polymer of Experimental Example 40 was used
instead of the fluorine-containing polymer having
.alpha.-fluoroacryloyl group and obtained in Experimental Example
30. Then physical properties of the antireflection film were
evaluated in the same manner as in (3) and (4) of Experimental
Example 34. The results are shown in Table 6.
6 TABLE 6 Experimental Example 34 35 36 37 39 41 Substrate film
Acryl Acryl Acryl Acryl Acryl Acryl Content of end OH group 30 0 30
0 46 4 (% by mole) Adding amount of PFPE 1.0 1.0 None None None
None compound.sup.1) (% by weight) Curable fluorine-containing Exp.
Ex. 23 Exp. Ex. 30 Exp. Ex. 23 Exp. Ex. 30 Exp. Ex. 38 Exp. Ex. 40
polymer Content of --O(C.dbd.O)CF.dbd.CH.sub.2 group 70 62 -- -- 54
38 (% by mole) Active energy curing initiator Fluorine- Fluorine-
-- -- Fluorine- Fluorine- containing containing containing
containing initiator.sup.2) initiator.sup.2) initiator.sup.2)
initiator.sup.2) Proportion to polymer 10 10 -- -- 10 10 (% by
weight) Amount of ultraviolet irradiation 1,500 mJ 1,500 mJ -- --
1,500 mJ 1,500 mJ (mJ/cm.sup.2) Reflectance of one side of film (%)
1.4 1.5 -- -- 1.1 1.4 Pencil hardness 2H 3H -- -- H 2H Contact
angle Water 105.5 98.3 89.5 95.5 105 93 n-HD 62.8 59.6 50.5 51.7
61.5 54.7 .gamma.s 16.1 18.7 23.8 21.3 16.5 21.6
[0644] 1) PFPE Compound 79
[0645] 2) Fluorine-Containing Energy Curing Initiator 80
EXPERIMENTAL EXAMPLES 42 and 43
[0646] (Preparation of Fluorine-Containing Resin Composition
Possessing Improved Coatability to PET Film)
[0647] The MEK solutions of fluorine-containing polymer having
.alpha.-fluoroacryloyl group which were obtained in Experimental
Example 23 (Experimental Example 42) and Experimental Example 30
(Experimental Example 43) were concentrated to adjust a
concentration thereof to 50% by weight, respectively. Then to 2 g
of the concentrated MEK solution were added 14 g of MIBK and 4 g of
2,2,3,3-tetrafluoropropanol (HCF.sub.2CF.sub.2CH.sub.2OH). Further
thereto was added, as an active energy curing initiator, 1.0 g of a
solution obtained by dissolving a fluorine-containing energy curing
initiator in HCFC-225 in a concentration of 10% by weight, and thus
uniform solutions were obtained.
EXPERIMENTAL EXAMPLES 44 and 45
[0648] (Evaluation of Coatability to PET Film)
[0649] The coating compositions obtained in Experimental Example 42
(Experimental Example 44) and Experimental Example 43 (Experimental
Example 45) were coated on non-treated PET films, respectively with
a doctor blade so that a coating thickness became 2 .mu.m. The
coating films were observed while air-drying at room temperature.
The evaluation was carried out under the following criteria:
[0650] .largecircle.: Coating film is dried in a state of uniform
coating thickness and there is no interference pattern after the
drying.
[0651] .DELTA.: Coating film is dried in a state of uniform coating
thickness but there is a small interference pattern after the
drying.
[0652] x: After the coating, repelling of the solution occurs on
the PET film and there are many interference patterns in a
concentric form after the drying. The results are shown in Table
7.
EXPERIMENTAL EXAMPLES 46 and 47
[0653] MEK was added to the solutions of fluorine-containing
polymer having .alpha.-fluoroacryloyl group which were obtained in
Experimental Example 23 (Experimental Example 46) and Experimental
Example 30 (Experimental Example 47) to dilute the solutions and
adjust the polymer concentration to 5.0% by weight.
[0654] To 20 g of the obtained polymer solution was added, as an
active energy curing initiator, 1.0 g of a solution obtained by
dissolving the fluorine-containing energy curing initiator obtained
in Experimental Example 18 in MEK in a concentration of 10% by
weight to obtain uniform solutions. The same evaluation as in
Experimental Example 44 was carried out using the obtained
solutions. The results are shown in Table 7.
7 TABLE 7 Experimental Example 44 45 46 47 Substrate film PET PET
PET PET Curable fluorine-containing Exp. Ex. 23 Exp. Ex. 30 Exp.
Ex. 23 Exp. Ex. 30 polymer Content of --O(C.dbd.O)CF.dbd.CH.sub.2
group 70 62 70 2 (% by mole) Active energy curing initiator
Fluorine- Fluorine- Fluorine- Fluorine- containing containing
containing containing initiator.sup.1) initiator.sup.1)
initiator.sup.1) initiator.sup.1) Proportion to polymer 10 10 10 10
(% by weight) Components of solvent MEK (% by weight) 5 5 100 100
MIBK (% by weight) 74 74 0 0 Fluorine-containing alcohol 21 21 0 0
(% by weight) Coatability on PET .largecircle. .largecircle. X
.DELTA.
[0655] 1) Fluorine-Containing Energy Curing Initiator 81
PREPARATION EXAMPLE 7
[0656] (Synthesis of Copolymer Comprising Fluorine-Containing Allyl
Ether Having OH Group and Tetrafluoroethylene)
[0657] A 100 ml stainless steel autoclave equipped with a valve,
pressure gauge and thermometer was charged with 10.0 g of
perfluoro(1,1,9,9-tetrah-
ydro-2,5-bistrifluoromethyl-3,6-dioxanonenol), 50 g of
CH.sub.3CCl.sub.2F (HCFC-141b) and 0.1 g of a methanol solution of
50% by weight of dinormalpropyl peroxy carbonate (NPP), and the
inside of a system was sufficiently replaced with nitrogen gas
while cooling with a dry ice/methanol solution. Then 8.0 g of
tetrafluoroethylene (TFE) was introduced through the valve. After
completion of the reaction carried out for 14 hours while shaking
at 40.degree. C., un-reacted monomer was released to terminate the
reaction.
[0658] A precipitated solid was removed and dissolved in acetone,
followed by re-precipitation with a solvent mixture of hexane and
HCFC-225 (20/80) to separate a copolymer. The copolymer was
vacuum-dried until a constant weight was reached. Thus 9.3 g of the
copolymer was obtained.
[0659] According to .sup.19F-NMR and .sup.1H-NMR analyses,
components of the copolymer were TFE and the fluorine-containing
allyl ether having OH group in a ratio of 48:52% by mole. The
number average molecular weight of the polymer was 24,000 according
to the GPC analysis using THF as a solvent and the weight average
molecular weight thereof was 36,100.
PREPARATION EXAMPLE 8
[0660] (Synthesis of Copolymer Comprising Fluorine-Containing Allyl
Ether Having OH Group and Chlorotrifluoroethylene)
[0661] A 100 ml stainless steel autoclave equipped with a valve,
pressure gauge and thermometer was charged with 10.0 g of
perfluoro(1,1,9,9-tetrah-
ydro-2,5-bistrifluoromethyl-3,6-dioxanonenol), 50 g of
CH.sub.3CCl.sub.2F (HCFC-141b) and 0.1 g of a methanol solution of
50% by weight of dinormalpropyl peroxy carbonate (NPP), and the
inside of a system was sufficiently replaced with nitrogen gas
while cooling with a dry ice/methanol solution. Then 5.8 g of
chlorotrifluoroethylene (CTFE) was introduced through the valve.
After completion of the reaction carried out for 20 hours while
shaking at 40.degree. C., un-reacted monomer was released to
terminate the reaction.
[0662] A precipitated solid was removed and dissolved in acetone,
followed by re-precipitation with a solvent mixture of hexane and
HCFC-141b (50/50) to separate a copolymer. The copolymer was
vacuum-dried until a constant weight was reached. Thus 5.7 g of the
copolymer was obtained.
[0663] According to .sup.19F-NMR and .sup.1H-NMR analyses,
components of the copolymer were CTFE and the fluorine-containing
allyl ether having OH group in a ratio of 35:65% by mole. The
number average molecular weight of the polymer was 10,500 according
to the GPC analysis using THF as a solvent and the weight average
molecular weight thereof was 7,200.
EXPERIMENTAL EXAMPLE 48
[0664] (Synthesis of Curable Fluorine-Containing Polymer Having
.alpha.-Fluoroacryloyl Group)
[0665] A 200 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 50 ml of
diethyl ether, 2.0 g of the fluorine-containing allyl ether
copolymer having hydroxyl which was obtained in Preparation Example
7 and 0.9 g of pyridine. Thereto was added dropwise a solution
obtained by dissolving 0.9 g of .alpha.-fluoroacrylic acid fluoride
CH.sub.2.dbd.CFCOF in 10 ml of diethyl ether in the same manner as
in Experimental Example 23. Thus a curable fluorine-containing
polymer (diethyl ether solution) was synthesized.
[0666] According to .sup.19F-NMR analysis, the polymer was a
copolymer comprising a fluorine-containing allyl ether having
--OCOCF.dbd.CH.sub.2 group and TFE in a ratio of 52:48% by
mole.
[0667] According to IR analysis, an absorption of a carbon-carbon
double bond and an absorption of C.dbd.O group were observed at the
same positions, respectively as in Experimental Example 23.
EXPERIMENTAL EXAMPLE 49
[0668] (Synthesis of Curable Fluorine-Containing Polymer Having
.alpha.-Fluoroacryloyl Group)
[0669] A 200 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 30 ml of
methyl isobutyl ketone, 3.0 g of the fluorine-containing allyl
ether copolymer having hydroxyl which was obtained in Preparation
Example 8 and 0.7 g of pyridine. Thereto was added dropwise a
solution obtained by dissolving 0.8 g of .alpha.-fluoroacrylic acid
fluoride CH.sub.2.dbd.CFCOF in 10 ml of methyl isobutyl ketone in
the same manner as in Experimental Example 23. Thus a curable
fluorine-containing polymer (methyl isobutyl ketone solution) was
synthesized.
[0670] According to .sup.19F-NMR analysis, the polymer was a
copolymer comprising a fluorine-containing allyl ether having
--OCOCF.dbd.CH.sub.2 group, a fluorine-containing allyl ether
having OH group and CTFE in a ratio of 50:15:35% by mole.
[0671] According to IR analysis, an absorption of a carbon-carbon
double bond and an absorption of C.dbd.O group were observed at the
same positions, respectively as in Experimental Example 23.
EXPERIMENTAL EXAMPLES 50 and 51
[0672] Refractive indices of curable fluorine-containing polymers
before and after curing were measured in the same manner as in (3)
and (4) of Experimental Example 24 except that the
fluorine-containing polymers having .alpha.-fluoroacryloyl group
which were obtained in Experimental Example 48 (Experimental
Example 50) and Experimental Example 49 (Experimental Example 51)
were used instead of the curable fluorine-containing polymer
obtained in Experimental Example 23. The results are shown in Table
8.
8 TABLE 8 Experimental Example 50 51 Curable fluorine- Exp. Ex. 48
Exp. Ex. 49 containing polymer Content of --O(CO)CF.dbd.CH.sub.2 52
50 group Refractive index Before curing 1.363 1.368 After curing
1.374 1.380
EXPERIMENTAL EXAMPLE 52
[0673] (Synthesis of Novel Fluorine-Containing Unsaturated
Compound)
[0674] A 200 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 20.4 g of
perfluoro(1,1,9,9-tetrahydro-2,5-bistrifluoromethyl-3,6-dioxanonenol):
82
[0675] 80 ml of diethyl ether and 4.3 g of pyridine, and was cooled
to 5.degree. C. or lower with ice.
[0676] Then a solution obtained by dissolving 5.1 g of
.alpha.-fluoroacrylic acid fluoride CH.sub.2.dbd.CFCOF in 20 ml of
diethyl ether was added thereto dropwise over about 30 minutes with
stirring in nitrogen gas stream.
[0677] After completion of the addition, the flask temperature was
raised to room temperature and the stirring was further continued
for 4.0 hours.
[0678] After the reaction, the ether solution was poured in an
excessive amount of water and an organic substance was extracted
with ether, followed by washing of the ether layer with water, 2%
hydrochloric acid solution, 5% NaCl solution and then water, drying
the ether layer with anhydrous magnesium sulfate and distilling off
the ether to obtain 23 g of an organic substance.
[0679] According to .sup.1H-NMR, .sup.19F-NMR and GC-Mass analyses,
the obtained product was recognized to be a novel
fluorine-containing unsaturated compound represented by: 83
[0680] According to IR analysis, two absorptions of carbon-carbon
double bond were observed at 1,661 cm.sup.-1 and 1,695 cm.sup.-1
and an absorption of C.dbd.O group was observed at 1,770
cm.sup.-1.
PREPARATION EXAMPLE 9
[0681] A 300 ml four-necked flask equipped with a reflux condenser,
thermometer, stirrer and dropping funnel was charged with 46.4 g of
2,3,3,5,6,6,8-pentafluoro-4,7,
10-trioxa-5,8-bistrifluoromethyl-12,13-epo- xytrideca-1-ene: 84
[0682] 20 g of acetic acid and 1.0 g of triethylamine, followed by
heating at 95.degree. to 105.degree. C. for four hours with
stirring.
[0683] After cooling to room temperature, a solution obtained by
mixing 10.0 g of 85% potassium hydroxide and 80 ml of methanol was
added dropwise over about 30 minutes at room temperature through
the dropping funnel. After completion of the addition, stirring was
carried out at room temperature for five hours.
[0684] After completion of the reaction, 44 ml of 17% hydrochloric
acid solution was added and the mixture was poured in a large
amount of water. Thereafter sodium bicarbonate was added until the
aqueous layer became neutral.
[0685] After neutralizing, washing with 5% NaHCO.sub.3 solution and
water were repeated. After drying of an ether layer with anhydrous
magnesium sulfate, the ether was distilled off to obtain 29 g of an
organic substance.
[0686] According to .sup.1H-NMR, .sup.19F-NMR, IR and Mass
analyses, the obtained product was a fluorine-containing allyl
ether compound having two hydroxyl groups and represented by the
formula: 85
EXPERIMENTAL EXAMPLE 53
[0687] (Synthesis of Novel Fluorine-Containing Unsaturated
Compound)
[0688] Reaction and isolation were carried out in the same manner
as in Experimental Example 52 except that 24.1 g of the
fluorine-containing allyl ether compound having two hydroxyl groups
which was obtained in Preparation Example 9 and represented by:
86
[0689] was used instead of
perfluoro(1,1,9,9-tetrahydro-2,5-bistrifluorome-
thyl-3,6-dioxanonenol and 8.3 g of pyridine and 10.2 g of
.alpha.-fluoroacrylic acid fluoride CH.sub.2.dbd.CFCOF were used.
Thus 19.0 g of an organic substance was obtained.
[0690] According to .sup.1H-NMR, .sup.19F-NMR and GC-Mass analyses,
the obtained product was a novel fluorine-containing unsaturated
compound represented by the formula: 87
[0691] According to IR analysis, two absorptions of carbon-carbon
double bond were observed at 1,661 cm.sup.-1 and 1,695 cm.sup.-1
and an absorption of C.dbd.O group was observed at 1,770
cm.sup.-1.
PREPARATION EXAMPLE 10
[0692] (Synthesis of Fluorine-Containing Allyl Ether Homopolymer
Having Hydroxyl)
[0693] Polymerization and refining of a polymer were carried out in
the same manner as in Preparation Example 1 except that 24.1 g of
the fluorine-containing allyl ether compound having two hydroxyl
groups which was obtained in Preparation Example 9 and represented
by: 88
[0694] was used instead of
perfluoro(1,1,9,9-tetrahydro-2,5-bistrifluorome-
thyl-3,6-dioxanonenol. Thus 13.5 g of a transparent colorless
polymer was obtained.
[0695] According to .sup.1H-NMR, .sup.19F-NMR and IR analyses, the
obtained polymer was a fluorine-containing polymer consisting of
the structural unit of the above-mentioned fluorine-containing
allyl ether and having two OH groups at each side chain.
EXPERIMENTAL EXAMPLE 54
[0696] (Synthesis of Curable Fluorine-Containing Polymer Having
.alpha.-Fluoroacryloyl Group)
[0697] Synthesis of a curable fluorine-containing polymer was
carried out in the same manner as in Experimental Example 1 except
that 4.8 g of the fluorine-containing allyl ether homopolymer
having OH groups at each side chain and obtained in Preparation
Example 10 was used instead of the fluorine-containing allyl ether
polymer having hydroxyl and obtained in Preparation Example 1, and
3.1 g of pyridine and 2.0 g of .alpha.-fluoroacrylic acid fluoride
were used.
[0698] According to .sup.19F-NMR analysis of the obtained ether
solution, the polymer was a polymer consisting of a structural unit
derived from the fluorine-containing allyl ether represented by the
formula: 89
[0699] The polymer was coated on a NaCl plate and formed into a
cast film at room temperature. According to IR analysis, an
absorption of a carbon-carbon double bond was observed at 1,660
cm.sup.-1 and an absorption of C.dbd.O group was observed at 1,770
cm.sup.-1. However an absorption of OH group could not be
observed.
INDUSTRIAL APPLICABILITY
[0700] According to the present invention, there can be provided a
curable fluorine-containing polymer which can realize a high
hardness by photo-curing while maintaining a low refractive
index.
[0701] Further there can be provided an antireflection film
possessing improved scratch resistance and abrasion resistance
while maintaining a reflection reducing effect, and an
antireflection-treated article provided with such an antireflection
film can be provided.
* * * * *