JP4702055B2 - 珪素含有高分子化合物及びその製造方法 - Google Patents
珪素含有高分子化合物及びその製造方法 Download PDFInfo
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- JP4702055B2 JP4702055B2 JP2005512082A JP2005512082A JP4702055B2 JP 4702055 B2 JP4702055 B2 JP 4702055B2 JP 2005512082 A JP2005512082 A JP 2005512082A JP 2005512082 A JP2005512082 A JP 2005512082A JP 4702055 B2 JP4702055 B2 JP 4702055B2
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- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229960004050 aminobenzoic acid Drugs 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940114079 arachidonic acid Drugs 0.000 description 1
- 235000021342 arachidonic acid Nutrition 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 229960004365 benzoic acid Drugs 0.000 description 1
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010511 deprotection reaction Methods 0.000 description 1
- 229960005215 dichloroacetic acid Drugs 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- RSIHJDGMBDPTIM-UHFFFAOYSA-N ethoxy(trimethyl)silane Chemical compound CCO[Si](C)(C)C RSIHJDGMBDPTIM-UHFFFAOYSA-N 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- POPACFLNWGUDSR-UHFFFAOYSA-N methoxy(trimethyl)silane Chemical compound CO[Si](C)(C)C POPACFLNWGUDSR-UHFFFAOYSA-N 0.000 description 1
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- ZIYVHBGGAOATLY-UHFFFAOYSA-N methylmalonic acid Chemical compound OC(=O)C(C)C(O)=O ZIYVHBGGAOATLY-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- POPVULPQMGGUMJ-UHFFFAOYSA-N octasilsesquioxane cage Chemical class O1[SiH](O[SiH](O2)O[SiH](O3)O4)O[SiH]4O[SiH]4O[SiH]1O[SiH]2O[SiH]3O4 POPVULPQMGGUMJ-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 229960002969 oleic acid Drugs 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- JXOHGGNKMLTUBP-HSUXUTPPSA-N shikimic acid Chemical compound O[C@@H]1CC(C(O)=O)=C[C@@H](O)[C@H]1O JXOHGGNKMLTUBP-HSUXUTPPSA-N 0.000 description 1
- JXOHGGNKMLTUBP-JKUQZMGJSA-N shikimic acid Natural products O[C@@H]1CC(C(O)=O)=C[C@H](O)[C@@H]1O JXOHGGNKMLTUBP-JKUQZMGJSA-N 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229960004274 stearic acid Drugs 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000012485 toluene extract Substances 0.000 description 1
- 125000005389 trialkylsiloxy group Chemical group 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/075—Silicon-containing compounds
- G03F7/0757—Macromolecular compounds containing Si-O, Si-C or Si-N bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C08G77/16—Polysiloxanes containing silicon bound to oxygen-containing groups to hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C08G77/18—Polysiloxanes containing silicon bound to oxygen-containing groups to alkoxy or aryloxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
- C09D183/06—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
- H01L21/02112—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
- H01L21/02123—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon
- H01L21/02126—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon the material containing Si, O, and at least one of H, N, C, F, or other non-metal elements, e.g. SiOC, SiOC:H or SiONC
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02225—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer
- H01L21/0226—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process
- H01L21/02282—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process liquid deposition, e.g. spin-coating, sol-gel techniques, spray coating
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/312—Organic layers, e.g. photoresist
- H01L21/3121—Layers comprising organo-silicon compounds
- H01L21/3122—Layers comprising organo-silicon compounds layers comprising polysiloxane compounds
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane
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Description
1.下記一般式(1)で表され、重量平均分子量が500〜500,000であるアルカリ可溶性珪素含有高分子化合物。
〔式中、A1は水酸基を有するかもしくはアルコキシ基を有するフェニル基、R1は炭素数1〜4のアルキレン基、mは0又は1、R2は炭素数1〜4のアルキル基(1分子中のR2は同種でも2種以上の異種の組み合わせであってもよい。)、s及びuは正の数であり、tは0又は正の数であって、0≦t/(s+u)≦1且つ0<u/s≦5である。〕
2.上記一般式(1)において、0≦t/(s+u)≦0.2且つ0.2≦u/s≦5であり、室温において固体である上記1記載のアルカリ可溶性珪素含有高分子化合物。
3.A 1 は水酸基及びアルコキシ基を有するフェニル基である上記1又は2記載のアルカリ可溶性珪素含有高分子化合物。
4.上記1乃至3のいずれかに記載のアルカリ可溶性珪素含有高分子化合物の製造方法であって、下記一般式(2)で表される加水分解性基含有オルガノシランsモル、下記一般式(3)で表される加水分解性基含有オルガノシランtモル及び下記一般式(4)で表される加水分解性基含有珪素化合物uモル〔但し、s及びuは正の数であり、tは0又は正の数であって、0≦t/(s+u)≦1且つ0<u/s≦5である。〕を、加水分解共縮合反応させることを特徴とするアルカリ可溶性珪素含有高分子化合物の製造方法。
A1(R1)mSiM1 3 (2)
〔式中、A1は水酸基を有するかもしくはアルコキシ基を有するフェニル基、R1は炭素数1〜4のアルキレン基、M1は加水分解性基、mは0又は1である。〕
〔式中、R2は炭素数1〜4のアルキル基、M2は加水分解性基である。〕
SiM3 4 (4)
〔式中、M3は加水分解性基である。〕
1.アルカリ可溶性珪素含有高分子化合物
本発明のアルカリ可溶性珪素含有高分子化合物(以下、「高分子化合物(I)」ともいう。)は、下記一般式(1)で表され、重量平均分子量が500〜500,000である。
〔式中、A1は水酸基を有するかもしくはアルコキシ基を有するフェニル基、R1は炭素数1〜4のアルキレン基、mは0又は1、R2は炭素数1〜4のアルキル基(1分子中のR2は同種でも2種以上の異種の組み合わせであってもよい。)、s及びuは正の数であり、tは0又は正の数であって、0≦t/(s+u)≦1且つ0<u/s≦5である。〕
〔式中、A1は水酸基を有するかもしくはアルコキシ基を有するフェニル基、R1は炭素数1〜4のアルキレン基、mは0又は1である。〕
〔式中、R2は炭素数1〜4のアルキル基である。〕
[Si−O4/2] (8)
A1の好ましい例として、オルトヒドロキシフェニル基、メタヒドロキシフェニル基、パラヒドロキシフェニル基、2,3−ジヒドロキシフェニル基、2,4−ジヒドロキシフェニル基、3,4−ジヒドロキシフェニル基、3,5−ジヒドロキシフェニル基、オルトメトキシフェニル基、メタメトキシフェニル基、パラメトキシフェニル基、2,3−ジメトキシフェニル基、2,4−ジメトキシフェニル基、3,4−ジメトキシフェニル基、3,5−ジメトキシフェニル基、オルトエトキシフェニル基、メタエトキシフェニル基、パラエトキシフェニル基、2,3−ジエトキシフェニル基、2,4−ジエトキシフェニル基、3,4−ジエトキシフェニル基、3,5−ジエトキシフェニル基、オルトイソプロポキシフェニル基、メタイソプロポキシフェニル基、パライソプロポキシフェニル基、2,3−ジ−イソプロポキシフェニル基、2,4−ジ−イソプロポキシフェニル基、3,4−ジ−イソプロポキシフェニル基、3,5−ジ−イソプロポキシフェニル基、オルト−tert−ブトキシフェニル基、メタ−tert−ブトキシフェニル基、パラ−tert−ブトキシフェニル基、2,3−ジ−tert−ブトキシフェニル基、2,4−ジ−tert−ブトキシフェニル基、3,4−ジ−tert−ブトキシフェニル基、3,5−ジ−tert−ブトキシフェニル基、2−メトキシ−3−ヒドロキシフェニル基、2−メトキシ−4−ヒドロキシフェニル基、3−メトキシ−4−ヒドロキシフェニル基、3−メトキシ−5−ヒドロキシフェニル基、2−ヒドロキシ−3−メトキシフェニル基、2−ヒドロキシ−4−メトキシフェニル基、3−ヒドロキシ−4−メトキシフェニル基、3−ヒドロキシ−5−メトキシフェニル基、2−エトキシ−3−ヒドロキシフェニル基、2−エトキシ−4−ヒドロキシフェニル基、3−エトキシ−4−ヒドロキシフェニル基、3−エトキシ−5−ヒドロキシフェニル基、2−ヒドロキシ−3−エトキシフェニル基、2−ヒドロキシ−4−エトキシフェニル基、3−ヒドロキシ−4−エトキシフェニル基、3−ヒドロキシ−5−エトキシフェニル基等が挙げられる。
本発明の高分子化合物(I)において、s≧2の場合、1分子中のA1は同種であってもよく、また、2種以上の異種の組み合わせであってもよい。
mは0又は1である。
本発明の高分子化合物(I)に含まれるR2は同種であってもよく、また、2種以上の異種の組み合わせであってよい。
本発明のアルカリ可溶性珪素含有高分子化合物の製造方法は、上記一般式(1)で表される高分子化合物(I)の製造方法であり、下記一般式(2)で表される加水分解性基含有オルガノシランsモル、下記一般式(3)で表される加水分解性基含有オルガノシランtモル及び下記一般式(4)で表される加水分解性基含有珪素化合物uモル〔但し、s及びuは正の数であり、tは0又は正の数であって、0≦t/(s+u)≦1且つ0<u/s≦5である。〕を、加水分解共縮合反応させるものである。
〔式中、A1は水酸基を有するかもしくはアルコキシ基を有するフェニル基、R1は炭素数1〜4のアルキレン基、M1は加水分解性基、mは0又は1である。〕
〔式中、R2は炭素数1〜4のアルキル基、M2は加水分解性基である。〕
SiM3 4 (4)
〔式中、M3は加水分解性基である。〕
上記一般式(3)で表される化合物としては、トリメチルメトキシシラン、トリメチルエトキシシラン等が挙げられる。
また、上記一般式(4)で表される化合物としては、テトラエトキシシラン等が挙げられる。
酸性触媒としては、無機酸及び有機酸を、各々、単独であるいは組み合わせて用いることができる。無機酸としては、例えば、塩酸、硫酸、燐酸、硝酸等が挙げられる。有機酸としては、例えば、酢酸、プロピオン酸、ブタン酸、ペンタン酸、ヘキサン酸、ヘプタン酸、オクタン酸、ノナン酸、デカン酸、シュウ酸、マレイン酸、メチルマロン酸、アジピン酸、セバシン酸、没食子酸、酪酸、メリット酸、アラキドン酸、シキミ酸、2−エチルヘキサン酸、オレイン酸、ステアリン酸、リノール酸、リノレイン酸、サリチル酸、安息香酸、p−アミノ安息香酸、p−トルエンスルホン酸、ベンゼンスルホン酸、モノクロロ酢酸、ジクロロ酢酸、トリクロロ酢酸、トリフルオロ酢酸、ギ酸、マロン酸、スルホン酸、フタル酸、フマル酸、クエン酸、酒石酸等が挙げられる。
金属キレート化合物としては、例えば、チタンキレート化合物、ジルコニウムキレート化合物、アルミニウムキレート化合物等が挙げられる。
本発明の高分子化合物(I)の製造方法においては、酸性触媒を用いることが好ましく、揮発性の高い塩酸、硝酸等が特に好ましい。
トリアルキルシリル基で保護した場合には、このトリアルキルシリル基が加水分解して、上記一般式(7)で表される1官能性シロキサン単位として本発明の珪素含有高分子化合物中に取り込まれ得る。
1.アルカリ可溶性珪素含有高分子化合物の製造
参考例1〔3−(3−メトキシ−4−ヒドロキシフェニル)プロピルトリエトキシシランの合成〕
撹拌機、還流管、滴下ロート及び温度計を備えた四つ口フラスコに、3−(3−メトキシ−4−ヒドロキシフェニル)プロペン164g(1.0モル)と、塩化白金酸の2質量%イソプロパノール溶液を白金量換算で100ppmとを加え、50〜60℃で加熱撹拌しながら、滴下ロートよりトリエトキシシラン164g(1.0モル)を5時間かけて滴下し、反応させた。反応終了後、減圧蒸留して目的物〔3−(3−メトキシ−4−ヒドロキシフェニル)プロピルトリエトキシシラン〕を289g(0.88モル)得た。収率は88%であった。
反応生成物の物性を以下に示す。
沸点 : 130℃/2mmHg
1H−NMR δ(ppm):
0.6〜0.8(m,2H),1.1〜1.3(m,9H),1.6〜1.9(m,2H),2.4〜2.6(m,2H),3.5〜4.1(m,9H),5.48(s,1H),6.5〜6.7(m,2H),6.7〜7.0(m,1H)
撹拌機、還流管、滴下ロート及び温度計を備えた四つ口フラスコに、参考例1で得られた3−(3−メトキシ−4−ヒドロキシフェニル)プロピルトリエトキシシラン65.7g(0.2モル)、テトラエトキシシラン33.3g(0.16モル)、ヘキサメチルジシロキサン3.2g(0.02モル)及びトルエン37.0gを加え、70℃で加熱撹拌しながら、水20g、濃塩酸0.5g及びエタノール10gの混合物を約1時間かけて滴下し、反応させた。
滴下終了後、75℃で4時間還流を続けた。次いで、反応系に水150gを加え、静置することで2層に分離させた。高分子成分を含む下層を分取し、上層をトルエン100gにより抽出した。次いで、トルエン抽出物と上記高分子成分とを合わせ、水分定量受器を装着したフラスコに戻し、共沸によって水及びエタノールを留出させた。冷却後、ろ過、濃縮により、珪素含有高分子化合物47.8gを得た。収率は85%であった。
〔式中、l:m:n=1:0.2:0.8である。〕
分子量(GPC,テトラヒドロフラン溶媒,標準ポリスチレン換算):
Mw=8.5×103
Mn=4.4×103
軟化点 : 95〜100℃
1H−NMR δ(ppm):
−0.4〜0.4(br,1.8H),0.5〜2.7(br,6H),3.4〜4.3(br,3H),6.4〜7.2(br,3H)
29Si−NMR δ(ppm):
−114〜−102(br,0.79Si),−70〜−63(br,1Si),8〜15(br,0.18Si)
上記実施例1−1と同様にして、参考例1で得られた3−(3−メトキシ−4−ヒドロキシフェニル)プロピルトリエトキシシランを、テトラエトキシシラン、ヘキサメチルジシロキサン等と表1に示す比率で仕込み、珪素含有高分子化合物を製造した。反応生成物の物性は、表1に併記した。
撹拌機、還流管、滴下ロート及び温度計を備えた四つ口フラスコに、p−(tert−ブトキシ)スチレン176g(1.0モル)と、塩化白金酸の2質量%イソプロパノール溶液を白金量換算で100ppmとを加え、50〜60℃で加熱撹拌しながら、滴下ロートよりトリエトキシシラン164g(1.0モル)を5時間かけて滴下し、反応させた。反応終了後、減圧蒸留して目的物〔2−p−(tert−ブトキシ)フェニルエチルトリエトキシシラン〕を313g(0.92モル)得た。収率は92%であった。
反応生成物の物性を以下に示す。
沸点 : 115℃/3mmHg
1H−NMR δ(ppm):
0.5〜0.7(m,2H),1.0〜1.5(m,18H),2.4〜2.7(m,2H)、3.5〜4.1(m,6H),6.5〜6.7(m,2H),6.7〜7.0(m,2H)
撹拌機、還流管、滴下ロート及び温度計を備えた四つ口フラスコに、参考例2で得られた2−p−(tert−ブトキシ)フェニルエチルトリエトキシシラン68.1g(0.2モル)、テトラエトキシシラン33.3g(0.16モル)、ヘキサメチルジシロキサン3.2g(0.02モル)及びトルエン41.5gを加え、70℃で加熱撹拌しながら、水20g、濃塩酸0.5g及びエタノール10gの混合物を約1時間かけて滴下し、反応させた。その後、実施例1−1と同様にして、分離、濃縮により珪素含有高分子化合物51.7gを得た。収率は88%であった。
〔式中、l:m:n=1:0.2:0.8である。〕
分子量(GPC,テトラヒドロフラン溶媒,標準ポリスチレン換算):
Mw=5.6×103
Mn=3.2×103
軟化点 : 120〜130℃
1H−NMR δ(ppm):
−0.4〜0.4(br,1.8H),0.5〜2.7(br,13H),6.4〜7.2(br,4H)
29Si−NMR δ(ppm):
−113〜−101(br,0.78Si),−72〜−64(br,1Si),7〜15(br,0.15Si)
Claims (4)
- 上記一般式(1)において、0≦t/(s+u)≦0.2且つ0.2≦u/s≦5であり、室温において固体である請求項1記載のアルカリ可溶性珪素含有高分子化合物。
- A 1 は水酸基及びアルコキシ基を有するフェニル基である請求項1又は2記載のアルカリ可溶性珪素含有高分子化合物。
- 請求項1乃至3のいずれかに記載のアルカリ可溶性珪素含有高分子化合物の製造方法であって、
下記一般式(2)で表される加水分解性基含有オルガノシランsモル、下記一般式(3)で表される加水分解性基含有オルガノシランtモル及び下記一般式(4)で表される加水分解性基含有珪素化合物uモル〔但し、s及びuは正の数であり、tは0又は正の数であって、0≦t/(s+u)≦1且つ0<u/s≦5である。〕を、加水分解共縮合反応させることを特徴とするアルカリ可溶性珪素含有高分子化合物の製造方法。
A1(R1)mSiM1 3 (2)
〔式中、A1は水酸基を有するかもしくはアルコキシ基を有するフェニル基、R1は炭素数1〜4のアルキレン基、M1は加水分解性基、mは0又は1である。〕
SiM3 4 (4)
〔式中、M3は加水分解性基である。〕
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- 2004-07-29 CN CNB2004800217342A patent/CN100430432C/zh not_active Expired - Fee Related
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- 2004-07-29 KR KR1020107028035A patent/KR101100463B1/ko active IP Right Grant
- 2004-07-29 KR KR1020067001936A patent/KR101054569B1/ko active IP Right Grant
- 2004-07-29 CN CN2008100917320A patent/CN101255233B/zh not_active Expired - Lifetime
- 2004-07-29 WO PCT/JP2004/010853 patent/WO2005010077A1/ja active Application Filing
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Also Published As
Publication number | Publication date |
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CN101255233B (zh) | 2011-12-28 |
JP5601212B2 (ja) | 2014-10-08 |
KR20110008327A (ko) | 2011-01-26 |
CN100430432C (zh) | 2008-11-05 |
KR101054569B1 (ko) | 2011-08-04 |
CN1829762A (zh) | 2006-09-06 |
US7811637B2 (en) | 2010-10-12 |
US20070134424A1 (en) | 2007-06-14 |
WO2005010077A1 (ja) | 2005-02-03 |
KR20060052926A (ko) | 2006-05-19 |
US8329815B2 (en) | 2012-12-11 |
EP1650250A4 (en) | 2009-08-12 |
KR101100463B1 (ko) | 2011-12-29 |
US20100029841A1 (en) | 2010-02-04 |
JP2011102399A (ja) | 2011-05-26 |
EP2159249A1 (en) | 2010-03-03 |
EP1650250A1 (en) | 2006-04-26 |
JPWO2005010077A1 (ja) | 2006-11-30 |
CN101255233A (zh) | 2008-09-03 |
EP2159249B1 (en) | 2014-09-10 |
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