JP2000063415A5 - - Google Patents
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- JP2000063415A5 JP2000063415A5 JP1998227992A JP22799298A JP2000063415A5 JP 2000063415 A5 JP2000063415 A5 JP 2000063415A5 JP 1998227992 A JP1998227992 A JP 1998227992A JP 22799298 A JP22799298 A JP 22799298A JP 2000063415 A5 JP2000063415 A5 JP 2000063415A5
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- compound
- aryl
- transition metal
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- -1 oxy compound Chemical class 0.000 claims description 9
- 150000002894 organic compounds Chemical class 0.000 claims description 2
- 150000003623 transition metal compounds Chemical class 0.000 claims 2
- 150000001336 alkenes Chemical class 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 150000002902 organometallic compounds Chemical class 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000004432 carbon atoms Chemical group C* 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 125000004104 aryloxy group Chemical group 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-Methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000002102 aryl alkyloxo group Chemical group 0.000 description 1
- 125000005110 aryl thio group Chemical group 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000001727 boranediyl group Chemical group [H]B(*)* 0.000 description 1
- 125000002515 boranetriyl group Chemical group *B(*)* 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 description 1
- 125000005587 carbonate group Chemical group 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical group 0.000 description 1
- 239000004643 cyanate ester Chemical group 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000005022 dithioester group Chemical group 0.000 description 1
- LDLDYFCCDKENPD-UHFFFAOYSA-N ethenylcyclohexane Chemical compound C=CC1CCCCC1 LDLDYFCCDKENPD-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- 150000002391 heterocyclic compounds Chemical group 0.000 description 1
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 description 1
- 125000005638 hydrazono group Chemical group 0.000 description 1
- 125000005462 imide group Chemical group 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 125000002462 isocyano group Chemical group *[N+]#[C-] 0.000 description 1
- ZBKFYXZXZJPWNQ-UHFFFAOYSA-N isothiocyanate group Chemical group [N-]=C=S ZBKFYXZXZJPWNQ-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000000109 phenylethoxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])O* 0.000 description 1
- FZTWZIMSKAGPSB-UHFFFAOYSA-N phosphide(3-) Chemical group [P-3] FZTWZIMSKAGPSB-UHFFFAOYSA-N 0.000 description 1
- 125000001863 phosphorothioyl group Chemical group *P(*)(*)=S 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000007970 thio esters Chemical group 0.000 description 1
- 125000003441 thioacyl group Chemical group 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M thiocyanate group Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- 125000000101 thioether group Chemical group 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N tin hydride Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Description
上記R55は水素原子または20個までの非水素原子をもつアルキル、アリール、シリル、ハロゲン化アルキル、ハロゲン化アリール基およびそれらの組合せから選ばれた基であり、R52は炭素原子数1〜10のアルキル、炭素原子数6〜10のアリール基若しくは炭素原子数7〜10のアラルキル基であるか、または1個若しくはそれ以上のR55と30個までの非水素原子の縮合環系を形成してもよい。
R 55 is a group selected from a hydrogen atom or an alkyl, aryl, silyl, halogenated alkyl, halogenated aryl group and combinations thereof having up to 20 non-hydrogen atoms, and R 52 is a group having 1 to 10 alkyls, aryl groups having 6 to 10 carbon atoms, or aralkyl groups having 7 to 10 carbon atoms, or forming a condensed ring system of one or more R 55 and up to 30 non-hydrogen atoms May be.
また、上記炭化水素基は、他の炭化水素基で置換されていてもよく、たとえば、ベンジル、クミルなどのアリール基置換アルキル基などが挙げられる。さらにまた、上記炭化水素基は、ヘテロ環式化合物残基;アルコキシ基、アリーロキシ基、エステル基、エーテル基、アシル基、カルボキシル基、カルボナート基、ヒドロキシ基、ペルオキシ基、カルボン酸無水物基などの酸素含有基;アミノ基、イミノ基、アミド基、イミド基、ヒドラジノ基、ヒドラゾノ基、ニトロ基、ニトロソ基、シアノ基、イソシアノ基、シアン酸エステル基、アミジノ基、ジアゾ基、アミノ基がアンモニウム塩となったものなどの窒素含有基;ボランジイル基、ボラントリイル基、ジボラニル基などのホウ素含有基;メルカプト基、チオエステル基、ジチオエステル基、アルキルチオ基、アリールチオ基、チオアシル基、
チオエーテル基、チオシアン酸エステル基、イソチアン酸エステル基、スルホンエステル基、スルホンアミド基、チオカルボキシル基、ジチオカルボキシル基、スルホ基、スルホニル基、スルフィニル基、スルフェニル基などのイオウ含有基;ホスフィド基、ホスホリル基、チオホスホリル基、ホスファト基などのリン含有基、ケイ素含有基、ゲルマニウム含有基、またはスズ含有基を有していてもよい。
The hydrocarbon group may be substituted with other hydrocarbon groups, and examples thereof include aryl group-substituted alkyl groups such as benzyl and cumyl. Furthermore, the hydrocarbon group is a heterocyclic compound residue; alkoxy group , aryloxy group, ester group, ether group, acyl group, carboxyl group, carbonate group, hydroxy group, peroxy group, carboxylic anhydride group, etc. Oxygen-containing group: amino group, imino group, amide group, imide group, hydrazino group, hydrazono group, nitro group, nitroso group, cyano group, isocyano group, cyanate ester group, amidino group, diazo group, amino group is ammonium salt Nitrogen-containing groups such as those obtained; boron-containing groups such as boranediyl group, boranetriyl group, diboranyl group; mercapto group, thioester group, dithioester group, alkylthio group, arylthio group, thioacyl group,
Sulfur-containing groups such as thioether groups, thiocyanate groups, isothiocyanate groups, sulfone ester groups, sulfonamido groups, thiocarboxyl groups, dithiocarboxyl groups, sulfo groups, sulfonyl groups, sulfinyl groups, sulfenyl groups; phosphide groups, It may have a phosphorus-containing group such as a phosphoryl group, a thiophosphoryl group, or a phosphato group, a silicon-containing group, a germanium-containing group, or a tin-containing group.
酸素含有基としては、前記R1〜R6で例示したものと同様のものが挙げられ、具体的には、ヒドロキシ基;メトキシ、エトキシ、プロポキシ、ブトキシなどのアルコキシ基;フェノキシ、メチルフェノキシ、ジメチルフェノキシ、ナフトキシなどのアリーロキシ基;フェニルメトキシ、フェニルエトキシなどのアリールアルコキシ基;アセトキシ基;カルボニル基などが挙げられるが、これらに限定されるものではない。
Examples of the oxygen-containing group include the same groups as those exemplified above for R 1 to R 6 , specifically, a hydroxy group; an alkoxy group such as methoxy, ethoxy, propoxy, butoxy; phenoxy, methylphenoxy, dimethyl Examples include, but are not limited to, aryloxy groups such as phenoxy and naphthoxy; arylalkoxy groups such as phenylmethoxy and phenylethoxy; acetoxy groups; carbonyl groups and the like.
有機化合物としては、粒径が10〜300μmの範囲にある顆粒状ないしは微粒子状固体を挙げることができる。具体的には、エチレン、プロピレン、1−ブテン、4−メチル−1−ペンテンなどの炭素原子数が2〜14のα−オレフィンを主成分として生成される(共)重合体またはビニルシクロヘキサン、スチレンを主成分として生成される(共)重合体、およびそれらの変成体を例示することができる。 Examples of the organic compound include granular or fine particle solids having a particle size in the range of 10 to 300 μm. Specifically, a (co) polymer produced mainly from an α-olefin having 2 to 14 carbon atoms such as ethylene, propylene, 1-butene, 4-methyl-1-pentene, vinylcyclohexane, styrene the generated as the main component (co) polymers can be exemplified by Oyo originator these metamorphic body.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22799298A JP3900699B2 (en) | 1998-08-12 | 1998-08-12 | Olefin polymerization catalyst and olefin polymerization method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22799298A JP3900699B2 (en) | 1998-08-12 | 1998-08-12 | Olefin polymerization catalyst and olefin polymerization method |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2000063415A JP2000063415A (en) | 2000-02-29 |
JP2000063415A5 true JP2000063415A5 (en) | 2005-05-19 |
JP3900699B2 JP3900699B2 (en) | 2007-04-04 |
Family
ID=16869484
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP22799298A Expired - Lifetime JP3900699B2 (en) | 1998-08-12 | 1998-08-12 | Olefin polymerization catalyst and olefin polymerization method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3900699B2 (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1303543A1 (en) * | 2000-07-17 | 2003-04-23 | Univation Technologies LLC | A catalyst system and its use in a polymerization process |
CN100482706C (en) * | 2000-07-26 | 2009-04-29 | 三井化学株式会社 | Polymer and process for producing same |
JP2002105132A (en) * | 2000-07-26 | 2002-04-10 | Mitsui Chemicals Inc | Polymer and method for producing the same |
US6897273B2 (en) | 2000-12-04 | 2005-05-24 | Univation Technologies, Llc | Catalyst composition, method of polymerization and polymer therefrom |
US7879950B2 (en) * | 2003-05-13 | 2011-02-01 | Mitsui Chemicals, Inc. | Solvent dispersion of composite resin and uses thereof |
JP5154754B2 (en) * | 2005-01-31 | 2013-02-27 | 三井化学株式会社 | Ethylene polymer and molded product obtained therefrom |
WO2011040753A2 (en) * | 2009-09-29 | 2011-04-07 | 주식회사 엘지화학 | Supported hybrid metallocene catalyst comprising three compounds, and method for preparing same |
JP5597102B2 (en) * | 2009-11-13 | 2014-10-01 | 三井化学株式会社 | Olefin polymerization catalyst and process for producing olefin polymer |
-
1998
- 1998-08-12 JP JP22799298A patent/JP3900699B2/en not_active Expired - Lifetime
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