## Abstract ^13^C NMR analysis of relatively low‐molecular‐weight polypropylenes prepared using the catalyst system MgCl~2~/TiCl~4~/phthalate ester‐AlEt~3~‐external Lewis base has revealed the presence of up to around 20% butyl (__n__‐Bu) chain ends, indicative of regioirregular (2,1‐) monomer inse
Propene polymerization in the presence of MgCl2-supported Ziegler-Natta catalysts, 5. Microstructural characterization of the “isotactic” (heptane-insoluble) polypropene fractions
✍ Scribed by Vincenzo Busico; Roberta Cipullo; Paolo Corradini; Rosanna De Biasio
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 392 KB
- Volume
- 196
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
The stereosequence distribution in the heptane‐insoluble fraction of polypropene samples prepared with a number of MgCl~2~‐supported catalysts was analyzed in detail by means of ^13^CNMR. The results indicate that what is conventionally taken as “isotactic” polypropene is normally a stereoblock polymer, in which at least part of the macromolecules contain long isotactic blocks spaced by much shorter “syndiotactoid” sequences. This implies that the active sites responsible for the formation of the two types of stereosequences are able to interconvert reversibly on the surface of the MgCl~2~ support in times which may be shorter than the average growth times of the polymer molecules. Possible models of active sites apt to explain the observed polymerization behavior are also briefly discussed.
📜 SIMILAR VOLUMES
Investigation of the effects of hydrogen and different external donors on the stereoregularity and chain-end distribution of polypropylene prepared using MgCl,/TiCl,/phthalate ester-AIEt,alkoxysilane catalyst systems has not only confirmed the importance of regiospecificity in relation to hydrogen a