- NOVEL LIGAND COMPOUND AND TRANSITION METAL COMPOUND
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The present invention relates to a novel ligand compound and a transition metal compound. According to the present invention, the ligand compound with a novel structure and the transition metal compound comprising the same can be usefully used as a polymerization catalyst, regarding the manufacture of a polyolefin-based polymer. In the present invention, provided is the ligand compound, which is represented by chemical formula 1.COPYRIGHT KIPO 2016
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Paragraph 0147; 0148; 0149; 0150; 0151
(2016/10/07)
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- METHOD OF PREPARING NOVEL LIGAND COMPOUND AND TRANSITION METAL COMPOUND
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The present invention relates to a novel ligand compound and a producing method of a transition metal compound. In the producing method according to one embodiment of the present invention, the novel ligand compound and the transition metal compound can be obtained by a simple method and high efficiency. In addition, the novel ligand compound and the transition metal compound obtained by the method of the present invention can be helpfully used as a catalyst of polymerization reaction in production of an olefin-based polymer.COPYRIGHT KIPO 2016
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Paragraph 0175; 0176; 0177; 0178; 0179
(2016/10/08)
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- CROSSLINKED METALLOCENE COMPOUND FOR OLEFIN POLYMERIZATION AND METHOD OF POLYMERIZING OLEFIN WITH THE SAME
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The bridged metallocene compound or the olefin polymerization catalyst which comprises the compound, enables high polymerization activity in polymerizing one or more monomers selected from ethylene and α-olefins. The bridged metallocene compound contains
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Page/Page column 28
(2010/02/12)
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- A sterically expanded "Constrained Geometry Catalyst" for highly active olefin polymerization and copolymerization: An unyielding comonomer effect
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The 14 A octamethyloctahydrodibenzofluorene moiety has been incorporated into a sterically expanded constrained geometry catalyst, Me2Si(η1-C29H36)(η1-N-tBu)ZrCl2·OEt2 (1). The solid-state structure suggests that the activated olefin polymerization catalyst is quite spatially accessible, rationalizing its extraordinary reactivity toward α-olefins. 1/MAO (MAO = methylaluminoxane) can be more reactive toward α-olefins than toward ethylene and exhibit activities that are linearly and continuously proportional to 4-methyl-1-pentene or 1-octene concentration in their copolymerizations with ethylene. Copyright
- Irwin, Levi J.,Reibenspies, Joseph H.,Miller, Stephen A.
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p. 16716 - 16717
(2007/10/03)
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- METALLOCENE COMPOUND, PROCESS FOR PRODUCING METALLOCENE COMPOUND, OLEFIN POLYMERIZATION CATALYST, PROCESS FOR PRODUCING POLYOLEFIN, AND POLYOLEFIN
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The metallocene compound according to the invention and the olefin polymerization catalyst containing the compound are intended to produce a catalyst capable of preparing an isotactic polymer with a high polymerization activity. The metallocene compound contains a substituted cyclopentadienyl group and a (substituted) fluorenyl group and has a structure wherein these groups are bridged by a hydrocarbon group or the like. The process for preparing a metallocene compound according to the invention is intended to selectively prepare a specific metallocene compound so as not to produce an isomer, and in this process an intermediate product is synthesized by a specific method. The process for preparing a polyolefin according to the invention is intended to prepare a polyolefin having excellent impact resistance and transparency, and this process comprises homopolymerizing an α-olefin of 3 to 8 carbon atoms or copolymerizing an olefin of 3 to 8 carbon atoms and another α-olefin in the presence of an olefin polymerization catalyst containing the above-mentioned metallocene compound.
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- Fonctionnalisation d'hydrocarbures aromatiques polycycliques. Introduction de fonctions alcool, acide ou amine sur le biphenyle, le fluorene ou le phenanthrene
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With aluminium chloride as a catalyst, 3-methyl-1,3-butanediol, a primary-tertiary diol, yielded Friedel-Crafts primary alcohols with fluorene and biphenyl.The monosubstituted derivatives have been characterized mainly by 13C nmr and polysubstituted products have been obtained with excess diol.With the same substrates and in the same conditions a tertiary-tertiary diol such as 2,5-dimethyl-2,5-hexanediol gave only mono or bicycloalkylated hydrocarbons.The reactions of phtalic anhydride with fluorene, biphenyl and phenanthrene have been studied and the monosubstituted products characterized mainly by 13C nmr by means of a relaxation reagent.Bifunctionalized derivatives were also obtained and identified in the case of fluorene and biphenyl.On the other hand, amino functional groups were introduced on fluorene either by transformation of acid functions or by more direct routes such as reaction with isatoic anhydride or p-toluenesulfonylanthranilic acid.Some results have been used for the functionalization of an industrial residue containing polycyclic aromatic hydrocarbons.
- Guilhemat, Robert,Pereyre, Michel,Petraud, Michel
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p. 334 - 344
(2007/10/02)
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