The figure shows the general structure of the C 1 -symmetric zirconocenes investigated in this work. We would like to apologize for any inconvenience this mistake may have caused.
Metallocene Catalysts for 1-Butene Polymerization
✍ Scribed by Luigi Resconi; Isabella Camurati; Federica Malizia
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 397 KB
- Volume
- 207
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Summary: Isotactic polybutenes of variable isotacticity and melting points of form I in the range 100–125 °C have been prepared with both C~2~‐ and C~1~‐symmetric zirconocenes. The C~1~‐symmetric zirconocenes bearing the bilateral symmetric 2,5‐dimethyl‐7__H__‐cyclopenta[1,2‐b:4,3‐b′]dithiophene ligand connected by a dimethylsilandiyl bridge to a substituted indenyl ligand produce iPB with higher molecular mass, up to 400 000 at polymerization temperature of 70 °C in liquid butene. The degree of isotacticity depends on the substitution pattern of the indenyl ligand. The correlations between microstructure and melting points of the crystalline forms I and II of iPB have been defined. Some relevant differences in catalyst selectivity between propylene and 1‐butene polymerizations have been identified.
Linear correlation of melting points of form I and form II in isotactic poly(1‐butene)s of different chain regularities.
magnified imageLinear correlation of melting points of form I and form II in isotactic poly(1‐butene)s of different chain regularities.
📜 SIMILAR VOLUMES
## Abstract 3‐Methyl‐1‐butene was polymerized in the presence of a number of homogeneous metallocene catalysts (co‐catalyst methylalumoxane). Contrary to literature reports, it was found that even the simplest __C__~2~‐symmetric metallocenes promote the isotactic polymerization of this monomer with
## Abstract 1‐Butene polyinsertion promoted by two typical __C__~2~‐symmetric zirconocene catalysts (i.e. __rac__‐ethylenebis(1‐indenyl)ZrCl~2~ (1) and __rac__‐dimethylsilylbis(1‐indenyl)ZrCl~2~) (2) was investigated under both hydrooligomerization and polymerization conditions and compared with th
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