912675-91-3Relevant academic research and scientific papers
Synthesis and structures of o-phenylene-bridged Cp/phosphinoamide titanium complexes
Ji Wu, Chun,Hoon Lee, Sang,Yun, Hoseop,Yeoul Lee, Bun
, p. 5638 - 5646 (2006)
Addition of R′2PCl to anilines substituted with di- or trimethylcyclopentadienyl unit at ortho-position affords ortho-phenylene-bridged Me2Cp or Me3Cp/phosophinoamide ligands, 2-(RMe2C5H2)C
Transition metal complexes, catalyst compositions containing the same, and olefin polymerization using the catalyst compositions
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Page/Page column 32, (2009/05/29)
Provided are a novel transition metal complex where a monocyclopentadienyl ligand to which an amido or alcoxy group is introduced is coordinated, a method of synthesizing the same, and olefin polymerization using the transition metal complex. Compared to
Transition metal complexes, catalyst compositions containing the same, and olefin polymerization using the catalyst compositions
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Page/Page column 10, (2008/06/13)
Provided are a novel transition metal complex where a monocyclopentadienyl ligand to which an amine-based group is introduced is coordinated, a method of synthesizing the same, and olefin polymerization using the transition metal complex In the novel tran
O-Phenylene-bridged Cp/sulfonamido titanium complexes for ethylene/1-octene copolymerization
Joe, Dae June,Wu, Chun Ji,Bok, Taekki,Lee, Eun Jung,Lee, Choong Hoon,Han, Won-Sik,Kang, Sang Ook,Lee, Bun Yeoul
, p. 4056 - 4062 (2007/10/03)
The Suzuki-coupling reaction of 2-(dihydroxyboryl)-3,4-dimethyl-2- cyclopenten-1-one (1) and 2-(dihydroxyboryl)-3-methyl-2-cyclopenten-1-one (2) with 2-bromoaniline derivatives affords cyclopentenone compounds (3-8) from which cyclopentadiene compounds, 4,6-R′2-2-(2,5-Me 2C5H3)C6H2NH2 (9-11) and 4,6-R′2-2-(2,3,5-Me3C5H 2)C6H2NH2 (12-14) are prepared. After sulfonation of the -NH2 group with p-TsCl, metallation is carried out by successive addition of Ti(NMe2)4 and Me2SiCl2 affording o-phenylene-bridged Cp/sulfonamido titanium dichloride complexes, [4,6-R′2-2-(2,5-Me 2C5H2)C6H2NSO 2C6H4CH3)]TiCl2 (R′ = H, 21; R′ = Me, 22; R′ = F, 23) and [4,6-R′2-2- (2,3,5-Me3C5H)C6H2NSO 2C6H4CH3)]TiCl2 (R′ = H, 24; R′ = Me, 25; R′ = F, 26). The molecular structures of 24 and [2-(2,5-Me2C5H2)C6H 4NSO2C6H4CH3)]Ti(NMe 2)2 (27) are determined by X-ray crystallography. The Cp(centroid)-Ti-N angle in 24 is smaller (100.90°) than that observed for the CGC (constrained-geometry catalyst), [Me2Si(η5- Me4Cp)(NtBu)]TiCl2 (107.6°) indicating a more "constrained feature" in 24 than in the CGC. Complex 24 shows the highest activity among the newly prepared complexes in ethylene/1-octene copolymerization but it is slightly inferior to the CGC in terms of activity, comonomer-incorporation ability, and molecular weight of the obtained polymers. The Royal Society of Chemistry 2006.
