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Metallocene catalysts for olefin polymerization: Annual review for 1996

โœ Scribed by Gregory G. Hlatky

Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
579 KB
Volume
181
Category
Article
ISSN
0010-8545

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โœฆ Synopsis

This review covers research in olefin polymerization by metallocene catalysts published in 1996. While metallocenes are generally defined as metal complexes with two cyclopentadienyl rings, this review will additionally cover catalysts containing only one cyclopentadienyl ring, as well as catalysts with ligands isolobal to cyclopentadienide. Included will be certain disclosures concerning cocatalyst preparation and use. Polymer properties and uses will not be covered.

๐Ÿ“œ SIMILAR VOLUMES

Post-Metallocene Catalysts for Olefin Po
Post-Metallocene Catalysts for Olefin Polymerization
โœ K. P. Bryliakov ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons โš– 11 KB ๐Ÿ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Single-site catalysts for olefin polymer
Single-site catalysts for olefin polymerization:: Annual review for 1997
โœ Gregory G Hlatky ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 992 KB

Papers, patents, and published patent applications from 1997 on olefin polymerization by single-site catalysts and processes in which they are used are reviewed. Included are disclosures on cocatalyst preparation, and the copolymerization of a-olefins and carbon monoxide by metal complexes.

Metallacyclic metallocene complexes as c
Metallacyclic metallocene complexes as catalysts for olefin polymerization
โœ Helmut G. Alt; Erik H. Licht; Andrea I. Licht; Katharina J. Schneider ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 553 KB

Metallacyclic metallocene complexes of titanium, zirconium and hafnium can be prepared by hydrogen elimination processes of suitable substituents such as -phenylalkyl or -alkenyl at the aromatic ligands. In some cases, the intermediates containing agostic hydride ligands can be isolated and characte