JPH0341123A - ポリ（ジシレン―エチレン）類の製造方法 - Google Patents

ポリ（ジシレン―エチレン）類の製造方法

Info

Publication number: JPH0341123A
Authority: JP; Japan
Prior art keywords: ethylene; polymer; poly; formula; disilene
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

JP1176057A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0547567B2 (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 JP1176057A priority Critical patent/JPH0341123A/ja

1991-02-21 Publication of JPH0341123A publication Critical patent/JPH0341123A/ja

1993-07-19 Publication of JPH0547567B2 publication Critical patent/JPH0547567B2/ja

Status Granted legal-status Critical Current

Links

239000005977 Ethylene Substances 0.000 title claims abstract description 23
238000004519 manufacturing process Methods 0.000 title claims description 10
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 title abstract description 8
229910052783 alkali metal Inorganic materials 0.000 claims abstract description 11
150000001340 alkali metals Chemical class 0.000 claims abstract description 11
125000000217 alkyl group Chemical group 0.000 claims abstract description 9
125000001424 substituent group Chemical group 0.000 claims abstract description 9
239000003085 diluting agent Substances 0.000 claims abstract description 7
239000000126 substance Substances 0.000 claims abstract description 6
229910052740 iodine Inorganic materials 0.000 claims abstract description 4
229910052801 chlorine Inorganic materials 0.000 claims abstract description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
229910052710 silicon Inorganic materials 0.000 claims description 3
239000010703 silicon Substances 0.000 claims description 3
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
229920000642 polymer Polymers 0.000 abstract description 13
238000000034 method Methods 0.000 abstract description 10
IVSPVXKJEGPQJP-UHFFFAOYSA-N 2-silylethylsilane Chemical compound [SiH3]CC[SiH3] IVSPVXKJEGPQJP-UHFFFAOYSA-N 0.000 abstract description 5
239000000919 ceramic Substances 0.000 abstract description 2
229920001002 functional polymer Polymers 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
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract 1
239000000463 material Substances 0.000 abstract 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
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 4
-1 ethylsilyl Chemical group 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000011734 sodium Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 3
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
VGQOKOYKFDUPPJ-UHFFFAOYSA-N chloro-[2-[chloro(dimethyl)silyl]ethyl]-dimethylsilane Chemical group C[Si](C)(Cl)CC[Si](C)(C)Cl VGQOKOYKFDUPPJ-UHFFFAOYSA-N 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
239000000203 mixture Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
229910052700 potassium Inorganic materials 0.000 description 3
239000011591 potassium Substances 0.000 description 3
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
238000000605 extraction Methods 0.000 description 2
239000002904 solvent Substances 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
CJWVKODUKBMKGN-UHFFFAOYSA-N CC[SiH](CC[SiH](CC)CCl)CCl Chemical compound CC[SiH](CC[SiH](CC)CCl)CCl CJWVKODUKBMKGN-UHFFFAOYSA-N 0.000 description 1
BSKSKJHGLWDKSC-UHFFFAOYSA-N I[Si](CC[Si](C)(C)I)(C)C Chemical compound I[Si](CC[Si](C)(C)I)(C)C BSKSKJHGLWDKSC-UHFFFAOYSA-N 0.000 description 1
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
241000206766 Pavlova Species 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
238000009835 boiling Methods 0.000 description 1
VKSREWXQBUQJCH-UHFFFAOYSA-N bromo-[2-[bromo(dimethyl)silyl]ethyl]-dimethylsilane Chemical compound C[Si](C)(Br)CC[Si](C)(C)Br VKSREWXQBUQJCH-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
238000001816 cooling Methods 0.000 description 1
YUFQWDZOCUTRAW-UHFFFAOYSA-N disiletane Chemical compound C1C[SiH2][SiH2]1 YUFQWDZOCUTRAW-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000010574 gas phase reaction Methods 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
239000011630 iodine Chemical group 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
229910052760 oxygen Inorganic materials 0.000 description 1
235000012162 pavlova Nutrition 0.000 description 1
229920003257 polycarbosilane Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Landscapes

Ceramic Products (AREA)
Silicon Polymers (AREA)

JP1176057A 1989-07-07 1989-07-07 ポリ（ジシレン―エチレン）類の製造方法 Granted JPH0341123A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP1176057A JPH0341123A (ja)	1989-07-07	1989-07-07	ポリ（ジシレン―エチレン）類の製造方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP1176057A JPH0341123A (ja)	1989-07-07	1989-07-07	ポリ（ジシレン―エチレン）類の製造方法

Publications (2)

Publication Number	Publication Date
JPH0341123A true JPH0341123A (ja)	1991-02-21
JPH0547567B2 JPH0547567B2 (fr)	1993-07-19

Family

ID=16006966

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP1176057A Granted JPH0341123A (ja)	1989-07-07	1989-07-07	ポリ（ジシレン―エチレン）類の製造方法

Country Status (1)

Country	Link
JP (1)	JPH0341123A (fr)

Cited By (3)

* 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
KR100398947B1 (ko) *	2000-11-28	2003-09-22	금호석유화학 주식회사	폴리알킬렌글리콜로 치환된 다가반응성（ｍｕｌｔｉ－ｒｅａｃｔｉｖｅ）규소화합물 및 그제조방법
KR20140107341A (ko)	2011-12-28	2014-09-04	니뽄 서모스탯 가부시키가이샤	유체 제어 밸브

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 JP1176057A patent/JPH0341123A/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 (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR100398947B1 (ko) *	2000-11-28	2003-09-22	금호석유화학 주식회사	폴리알킬렌글리콜로 치환된 다가반응성（ｍｕｌｔｉ－ｒｅａｃｔｉｖｅ）규소화합물 및 그제조방법
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
KR20140107341A (ko)	2011-12-28	2014-09-04	니뽄 서모스탯 가부시키가이샤	유체 제어 밸브

Also Published As

Publication number	Publication date
JPH0547567B2 (fr)	1993-07-19

Similar Documents

Publication	Publication Date	Title
Foucher et al.	1994	Synthesis, characterization, and properties of high molecular weight unsymmetrically substituted poly (ferrocenylsilanes)
JPS63309526A (ja)	1988-12-16	新規ポリシラザン及びその製造方法
JPH0341123A (ja)	1991-02-21	ポリ（ジシレン―エチレン）類の製造方法
US5204434A (en)	1993-04-20	Polycarbosilanes and process for preparing them
Bucca et al.	1997	Thermally and oxidatively stable thermosets derived from preceramic monomers
JP6938265B2 (ja)	2021-09-22	金属錯体およびその製造方法、当該金属錯体を含むオレフィン重合用触媒成分およびオレフィン重合用触媒、並びに、当該オレフィン重合用触媒を用いたα−オレフィン重合体の製造方法
JP6867761B2 (ja)	2021-05-12	金属錯体およびその製造方法、当該金属錯体を含むオレフィン重合用触媒成分およびオレフィン重合用触媒、並びに、当該オレフィン重合用触媒を用いたα−オレフィン重合体の製造方法
JP6938264B2 (ja)	2021-09-22	金属錯体およびその製造方法、当該金属錯体を含むオレフィン重合用触媒成分およびオレフィン重合用触媒、並びに、当該オレフィン重合用触媒を用いたα−オレフィン重合体及び共重合体の製造方法
Schroeder et al.	1969	Icosahedral carboranes. XI. Germanium and tin derivatives of o-, m-, and p-carborane and their polymers
KR101677734B1 (ko)	2016-11-18	전이 금속 화합물 및 폴리올레핀 합성용 촉매 조성물
JPH01252637A (ja)	1989-10-09	有機金属高分子化合物の製造方法
JP3631213B2 (ja)	2005-03-23	官能基を有するフェロセニレンシリレンポリマー及びその製造方法
JP2621310B2 (ja)	1997-06-18	ポリシランポリマーの製造法
JPS6049643B2 (ja)	1985-11-02	４−ヒドロキシ−４′−ビニルビフエニル重合体およびその製造法
JP4857475B2 (ja)	2012-01-18	遷移金属化合物、オレフィン重合用触媒およびオレフィンの重合方法
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
JPH0188A (ja)	1989-01-05	ジクロロシラン類の製造方法
JPH01292034A (ja)	1989-11-24	ポリ（アミドベンゾオキサゾール）樹脂の製造方法
JPS62263189A (ja)	1987-11-16	ジアリ−ルジハロシランの製造方法
JP2615420B2 (ja)	1997-05-28	ポリシラン類の製造法
JPS62292806A (ja)	1987-12-19	原子団移動重合法およびリビングポリマ−
US3422130A (en)	1969-01-14	(perfluoroaryl)ferrocenes and the synthesis thereof
Butler et al.	1969	The formation of linear polymers from diene monomers by the cyclic polymerization mechanism. IX. Further polymerization studies on silane monomers
JP2017203053A (ja)	2017-11-16	光学活性基を有する置換ポリアセチレン及びその製造方法
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

Legal Events

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