JPS62209111A - 新規な重合体およびその製造法 - Google Patents

新規な重合体およびその製造法

Info

Publication number: JPS62209111A
Authority: JP; Japan
Prior art keywords: formula; group; structural formula; molecular weight; polymer
Prior art date: 1986-03-11
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

JP5147686A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0441685B2 (cs

Inventor

Teiji Tsuruta

鶴田　禎二

Yukio Nagasaki

幸夫長崎

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.)

Individual

Original Assignee

Individual

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.)

1986-03-11

Filing date

1986-03-11

Publication date

1987-09-14

1986-03-11 Application filed by Individual filed Critical Individual

1986-03-11 Priority to JP5147686A priority Critical patent/JPS62209111A/ja

1987-09-14 Publication of JPS62209111A publication Critical patent/JPS62209111A/ja

1992-07-09 Publication of JPH0441685B2 publication Critical patent/JPH0441685B2/ja

Status Granted legal-status Critical Current

Links

229920000642 polymer Polymers 0.000 title claims abstract description 19
238000004519 manufacturing process Methods 0.000 title description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 8
239000000178 monomer Substances 0.000 claims abstract description 6
125000000217 alkyl group Chemical group 0.000 claims abstract description 5
125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 5
125000003118 aryl group Chemical group 0.000 claims abstract description 5
230000000379 polymerizing effect Effects 0.000 claims abstract description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
150000001875 compounds Chemical class 0.000 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
239000000126 substance Substances 0.000 claims 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
229910052799 carbon Inorganic materials 0.000 claims 2
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract description 11
-1 chlorosilane compound Chemical class 0.000 abstract description 7
238000000034 method Methods 0.000 abstract description 4
238000006116 polymerization reaction Methods 0.000 abstract description 4
239000003063 flame retardant Substances 0.000 abstract description 3
239000003505 polymerization initiator Substances 0.000 abstract description 3
150000003377 silicon compounds Chemical class 0.000 abstract description 3
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 abstract description 2
239000004342 Benzoyl peroxide Substances 0.000 abstract description 2
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract description 2
239000005046 Chlorosilane Substances 0.000 abstract description 2
235000019400 benzoyl peroxide Nutrition 0.000 abstract description 2
239000002131 composite material Substances 0.000 abstract description 2
150000002900 organolithium compounds Chemical class 0.000 abstract description 2
229920002120 photoresistant polymer Polymers 0.000 abstract description 2
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 abstract description 2
239000012442 inert solvent Substances 0.000 abstract 1
239000012528 membrane Substances 0.000 abstract 1
238000000862 absorption spectrum Methods 0.000 description 8
238000000921 elemental analysis Methods 0.000 description 8
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
LXLJJQUMSRUTQD-UHFFFAOYSA-N [(4-ethenylphenyl)-trimethylsilylmethyl]-trimethylsilane Chemical compound C[Si](C)(C)C([Si](C)(C)C)C1=CC=C(C=C)C=C1 LXLJJQUMSRUTQD-UHFFFAOYSA-N 0.000 description 5
239000007788 liquid Substances 0.000 description 5
239000000047 product Substances 0.000 description 5
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
239000001301 oxygen Substances 0.000 description 4
229910052760 oxygen Inorganic materials 0.000 description 4
125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000003440 styrenes Chemical class 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
239000003708 ampul Substances 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
239000011521 glass Substances 0.000 description 2
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
229920006254 polymer film Polymers 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
XOBKSJJDNFUZPF-UHFFFAOYSA-N Methoxyethane Chemical compound CCOC XOBKSJJDNFUZPF-UHFFFAOYSA-N 0.000 description 1
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
241000220317 Rosa Species 0.000 description 1
QZQAYMWKEUNFEH-UHFFFAOYSA-N [(4-ethenylphenyl)-triethylsilylmethyl]-triethylsilane Chemical compound CC[Si](CC)(CC)C([Si](CC)(CC)CC)C1=CC=C(C=C)C=C1 QZQAYMWKEUNFEH-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 1
238000011088 calibration curve Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000004020 conductor Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000010894 electron beam technology Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000001914 filtration Methods 0.000 description 1
WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
229920001002 functional polymer Polymers 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
238000005227 gel permeation chromatography Methods 0.000 description 1
239000003365 glass fiber Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
MHAJPDPJQMAIIY-UHFFFAOYSA-M hydroperoxide group Chemical group [O-]O MHAJPDPJQMAIIY-UHFFFAOYSA-M 0.000 description 1
150000002432 hydroperoxides Chemical class 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
FVFMYDCFRDYUCF-UHFFFAOYSA-N methyl(2-phenylethenyl)silane Chemical compound C[SiH2]C=CC1=CC=CC=C1 FVFMYDCFRDYUCF-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000000203 mixture Substances 0.000 description 1
239000003607 modifier Substances 0.000 description 1
QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
230000035699 permeability Effects 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
FWGNVBNJIIHYAR-UHFFFAOYSA-N phenyl(3-phenylbut-2-en-2-yl)silane Chemical compound CC(=C([SiH2]C1=CC=CC=C1)C)C1=CC=CC=C1 FWGNVBNJIIHYAR-UHFFFAOYSA-N 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
QSOKYXQHVHZSER-UHFFFAOYSA-N trimethyl(3-phenylprop-2-enyl)silane Chemical compound C[Si](C)(C)CC=CC1=CC=CC=C1 QSOKYXQHVHZSER-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
238000005406 washing Methods 0.000 description 1

Landscapes

Separation Using Semi-Permeable Membranes (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

JP5147686A 1986-03-11 1986-03-11 新規な重合体およびその製造法 Granted JPS62209111A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP5147686A JPS62209111A (ja)	1986-03-11	1986-03-11	新規な重合体およびその製造法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP5147686A JPS62209111A (ja)	1986-03-11	1986-03-11	新規な重合体およびその製造法

Publications (2)

Publication Number	Publication Date
JPS62209111A true JPS62209111A (ja)	1987-09-14
JPH0441685B2 JPH0441685B2 (cs)	1992-07-09

Family

ID=12888001

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP5147686A Granted JPS62209111A (ja)	1986-03-11	1986-03-11	新規な重合体およびその製造法

Country Status (1)

Country	Link
JP (1)	JPS62209111A (cs)

1986
- 1986-03-11 JP JP5147686A patent/JPS62209111A/ja active Granted

Also Published As

Publication number	Publication date
JPH0441685B2 (cs)	1992-07-09

Legal Events

Date	Code	Title	Description
2004-07-09	LAPS	Cancellation because of no payment of annual fees

Publication	Publication Date	Title
Horiguchi et al.	1988	High molecular weight polysilanes with phenol moieties
JPS6338379B2 (cs)	1988-07-29
Ito et al.	1996	Synthesis and properties of germanium‐containing poly (diphenylacetylenes)
JPS62209111A (ja)	1987-09-14	新規な重合体およびその製造法
Isobe et al.	1986	Polymerization of 1‐(trimethylsilyl)‐1‐propyne homologs containing two silicon atoms by tantalum‐and niobium‐based catalysts
JPH04134090A (ja)	1992-05-07	ホスファゼン誘導体及びその重合体
JPS62257908A (ja)	1987-11-10	新しい珪素を含む重合体及びその製造法
JPS62260808A (ja)	1987-11-13	オルト位に置換基を有するフエニルアセチレン重合体
JP2939016B2 (ja)	1999-08-25	３−（ビニルフェニルオキシ）プロピルシラン化合物の製造方法
JPS62215608A (ja)	1987-09-22	アルケニルシリル基含有高分子化合物の製法
JPS62257916A (ja)	1987-11-10	新しい珪素を含む共重合体及びその製造法
JPS58206611A (ja)	1983-12-01	トリアルキルシリルアセチレン類の重合方法
JPH0260925A (ja)	1990-03-01	ブロック−グラフト共重合体およびその製造方法
JPS62209117A (ja)	1987-09-14	新規な共重合体およびその製造法
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
JPS62292810A (ja)	1987-12-19	エチニル基を有する機能性重合体およびその製造法
JPS63141626A (ja)	1988-06-14	選択性気体透過膜
JPS6357644A (ja)	1988-03-12	ジメチルシロキサン系ブロツク共重合体の製造方法
JPS6356513A (ja)	1988-03-11	ポリ二置換アセチレンのシリル化物およびその製造方法
JPS6386725A (ja)	1988-04-18	グラフト共重合体の製造方法
JPS63295606A (ja)	1988-12-02	ハロゲンを含有する置換アセチレンポリマ−の製造方法
JPS60225606A (ja)	1985-11-09	選択性気体透過膜
SU311918A1 (ru)		Способ получения полилитийорганического инициатора анионной полимеризации
JPH0693039A (ja)	1994-04-05	珪素含有重合体およびその製造方法
JPS62209084A (ja)	1987-09-14	珪素を有する化合物