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Access to Ultra-High-Molecular Weight Poly(ethylene) and Activity Boost in the Presence of Cyclopentene With Group 4 Bis-Amido Complexes. | LitMetric

Access to Ultra-High-Molecular Weight Poly(ethylene) and Activity Boost in the Presence of Cyclopentene With Group 4 Bis-Amido Complexes.

Chempluschem

Institut für Polymerchemie, Lehrstuhl für Makromolekulare Stoffe und Faserchemie, Universität Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart (Germany), Fax: (+49) 711-685-64050.

Published: January 2014

Zr complexes of the type [Me Si{(NR)(6-{2-(diethylboryl)phenyl}pyridyl-2-yl-N)}ZrCl ⋅thf] (R=tBu (4), adamantyl (7 a); thf=tetrahydrofuran), [Me Si{(NAd)(6-{2-(diphenylboryl)phenyl}pyridyl-2-yl-N)}ZrCl ] (Ad=adamantyl (7 b)), the nonbridged half-titanocene complexes of the type [(N-{6-(2-diethylborylphenyl)pyrid-2-yl}-NR)Cp'TiCl ] (R=Me, Cp'=C H (12), Cp'=C Me (13)), and the titanium(IV)-based metallocene-type complex [bis{N-(6-{2-(diethylboryl)phenyl}pyrid-2-yl)NMe}TiCl ] (14) have been synthesized. The structures of complexes 7 b, 12, and 13 were determined by single-crystal X-ray diffraction analysis. In solution, complex 4 slowly rearranges to [Me Si{(N-tBu)(6-{2-(diethylboryl)phenyl}pyridyl-2-yl-N)} Zr] (4 a), the structure of which was unambiguously confirmed by single-crystal X-ray crystallography. Similarly, reaction of HfCl with Me Si({RNLi}{6-[2-(diethylboryl)phenyl]pyridyl-2-ylNLi}) yielded the corresponding Hf complexes [Me Si{(NR)(6-{2-(diethylboryl)phenyl}pyridyl-2-ylN)} Hf] (R=tBu (8) and Ad (9)). Upon activation of these complexes with methylalumoxane (MAO), complexes 4, 7 a, 7 b, and 12-14 showed activities up to 750 kg of polyethylene (PE)/mol  bar h in the homopolymerization of ethylene (E), producing mainly linear PE (high-density PE, HDPE) with molecular weights in the range of 1 800 000

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Source
http://dx.doi.org/10.1002/cplu.201300378DOI Listing

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