JPH0341122A - アリール置換ポリカルボシラン類の製造方法 - Google Patents

アリール置換ポリカルボシラン類の製造方法

Info

Publication number: JPH0341122A
Authority: JP; Japan
Prior art keywords: aryl; aryl group; substituted; substituent; formula
Prior art date: 1989-07-07
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Granted

Application number

JP1176056A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0547566B2 (fr

Inventor

Teruyuki Hayashi

輝幸林

Toshiaki Kobayashi

敏明小林

Masato Tanaka

正人田中

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

National Institute of Advanced Industrial Science and Technology AIST

Original Assignee

Agency of Industrial Science and Technology

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1989-07-07

Filing date

1989-07-07

Publication date

1991-02-21

1989-07-07 Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology

1989-07-07 Priority to JP1176056A priority Critical patent/JPH0341122A/ja

1991-02-21 Publication of JPH0341122A publication Critical patent/JPH0341122A/ja

1993-07-19 Publication of JPH0547566B2 publication Critical patent/JPH0547566B2/ja

Status Granted legal-status Critical Current

Links

229920003257 polycarbosilane Polymers 0.000 title claims abstract description 5
238000004519 manufacturing process Methods 0.000 title claims description 7
125000003118 aryl group Chemical group 0.000 claims abstract description 23
125000001424 substituent group Chemical group 0.000 claims abstract description 13
229910052783 alkali metal Inorganic materials 0.000 claims abstract description 9
150000001340 alkali metals Chemical class 0.000 claims abstract description 9
125000000217 alkyl group Chemical group 0.000 claims abstract description 9
229910052710 silicon Inorganic materials 0.000 claims abstract description 8
229910052740 iodine Inorganic materials 0.000 claims abstract description 4
IVSPVXKJEGPQJP-UHFFFAOYSA-N 2-silylethylsilane Chemical compound [SiH3]CC[SiH3] IVSPVXKJEGPQJP-UHFFFAOYSA-N 0.000 claims abstract description 3
229910052794 bromium Inorganic materials 0.000 claims abstract description 3
229910052801 chlorine Inorganic materials 0.000 claims abstract description 3
239000010703 silicon Substances 0.000 claims description 7
239000000126 substance Substances 0.000 claims description 5
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
239000011630 iodine Chemical group 0.000 claims description 2
239000005977 Ethylene Substances 0.000 abstract description 10
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 8
229920000642 polymer Polymers 0.000 abstract description 6
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract description 3
239000000919 ceramic Substances 0.000 abstract description 2
230000021615 conjugation Effects 0.000 abstract description 2
HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 abstract description 2
229910010271 silicon carbide Inorganic materials 0.000 abstract description 2
229910008045 Si-Si Inorganic materials 0.000 abstract 2
229910006411 Si—Si Inorganic materials 0.000 abstract 2
239000000463 material Substances 0.000 abstract 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
-1 trifluoromethylphenyl Chemical group 0.000 description 9
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000002904 solvent Substances 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000000034 method Methods 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000000203 mixture Substances 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
239000002994 raw material Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
125000003944 tolyl group Chemical group 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
239000000956 alloy Substances 0.000 description 1
229910045601 alloy Inorganic materials 0.000 description 1
CCSKNYZYRFCIPK-UHFFFAOYSA-N chloro-[2-[2-(chloromethyl)phenyl]ethyl]-dimethylsilane Chemical compound C[Si](C)(Cl)CCC1=CC=CC=C1CCl CCSKNYZYRFCIPK-UHFFFAOYSA-N 0.000 description 1
GTXZCZRTAKZLQI-UHFFFAOYSA-N chloromethyl-[2-[chloromethyl(phenyl)silyl]ethyl]-phenylsilane Chemical compound C=1C=CC=CC=1[SiH](CCl)CC[SiH](CCl)C1=CC=CC=C1 GTXZCZRTAKZLQI-UHFFFAOYSA-N 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
239000003921 oil Substances 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
239000002002 slurry Substances 0.000 description 1
238000000638 solvent extraction Methods 0.000 description 1
238000010183 spectrum analysis Methods 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Landscapes

Silicon Polymers (AREA)
Ceramic Products (AREA)

JP1176056A 1989-07-07 1989-07-07 アリール置換ポリカルボシラン類の製造方法 Granted JPH0341122A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP1176056A JPH0341122A (ja)	1989-07-07	1989-07-07	アリール置換ポリカルボシラン類の製造方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP1176056A JPH0341122A (ja)	1989-07-07	1989-07-07	アリール置換ポリカルボシラン類の製造方法

Publications (2)

Publication Number	Publication Date
JPH0341122A true JPH0341122A (ja)	1991-02-21
JPH0547566B2 JPH0547566B2 (fr)	1993-07-19

Family

ID=16006949

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP1176056A Granted JPH0341122A (ja)	1989-07-07	1989-07-07	アリール置換ポリカルボシラン類の製造方法

Country Status (1)

Country	Link
JP (1)	JPH0341122A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2002167438A (ja) *	2000-11-29	2002-06-11	Jsr Corp	ケイ素ポリマー、膜形成用組成物および絶縁膜形成用材料

Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS58153931A (ja) *	1982-03-10	1983-09-13	Hitachi Ltd	放射線および光感応性有機高分子材料

1989
- 1989-07-07 JP JP1176056A patent/JPH0341122A/ja active Granted

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS58153931A (ja) *	1982-03-10	1983-09-13	Hitachi Ltd	放射線および光感応性有機高分子材料

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2002167438A (ja) *	2000-11-29	2002-06-11	Jsr Corp	ケイ素ポリマー、膜形成用組成物および絶縁膜形成用材料

Also Published As

Publication number	Publication date
JPH0547566B2 (fr)	1993-07-19

Legal Events

Date	Code	Title	Description
2009-07-07	EXPY	Cancellation because of completion of term

Publication	Publication Date	Title
Price et al.	1942	Addition polymerization catalyzed by substituted acyl peroxides
US4841083A (en)	1989-06-20	Ladder polysilanes
JPH0341122A (ja)	1991-02-21	アリール置換ポリカルボシラン類の製造方法
US2963483A (en)	1960-12-06	Nu-glycidylpiperazine and method of making it
JPH05194749A (ja)	1993-08-03	両末端反応性ポリシラン及びその製造方法
JPS6312636A (ja)	1988-01-20	ジメチルフエニルシリルメチルポリシランおよびその製造法
JPH01252637A (ja)	1989-10-09	有機金属高分子化合物の製造方法
JPS6312637A (ja)	1988-01-20	１，２，２−トリメチル−１−フエニルポリジシランおよびその製造方法
JP2634430B2 (ja)	1997-07-23	はしご状ポリシラン類及びその製造方法
JPH0341123A (ja)	1991-02-21	ポリ（ジシレン―エチレン）類の製造方法
JP3083614B2 (ja)	2000-09-04	有機ポリゲルマンの製法
JPH06306040A (ja)	1994-11-01	光重合性ジアセチレン化合物
JPS603409B2 (ja)	1985-01-28	ポリアシルヒドラゾン及びその製造方法
JP2773362B2 (ja)	1998-07-09	キノキサリン―パラジウム錯体およびその製造方法
JPS5938957B2 (ja)	1984-09-20	シラトラン誘導体の合成法
JPS63260925A (ja)	1988-10-27	主鎖にジシラン結合を有するポリシロキサンおよびその製造法
JPH05202077A (ja)	1993-08-10	ビス（シロキシ）芳香環骨格、ビス（シロキシ）アルケン骨格を有するケイ素化合物、それらの製造方法、およびそれらを用いた感光性および／または耐熱性材料
JPS63310860A (ja)	1988-12-19	新規アゾアミジン化合物及びその塩
JPS63115869A (ja)	1988-05-20	新規環状アゾアミジン化合物及びその塩
US3422130A (en)	1969-01-14	(perfluoroaryl)ferrocenes and the synthesis thereof
SU1325053A1 (ru)	1987-07-23	Способ получени 3,3Ъ,4,4Ъ,5,5Ъ гексахлор-2,2Ъ-дитиенила
JP3506759B2 (ja)	2004-03-15	オキサジノン環含有化合物の製造方法
JPS6388189A (ja)	1988-04-19	トリメチルシリル基を有する２−オキサゾリン類
JPH05320354A (ja)	1993-12-03	短波長吸収帯を有するポリシラン
JPS62290729A (ja)	1987-12-17	ジクロロシランのビス（クロロシリル）メタンとの共重合による生成物とその利用

JPH0341122A - アリール置換ポリカルボシラン類の製造方法 - Google Patents

Info

Links

Landscapes

Priority Applications (1)

Applications Claiming Priority (1)

Publications (2)

Family

ID=16006949

Family Applications (1)

Country Status (1)

Cited By (1)

Citations (1)

Patent Citations (1)

Cited By (1)

Also Published As

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