Polymerization of t‐butyl thiirane. II. Polymerization of enantiomerically enriched monomer. Mechanism of stereoelective process
- 1 June 1979
- journal article
- research article
- Published by Wiley in Journal of Polymer Science: Polymer Chemistry Edition
- Vol. 17 (6) , 1595-1604
- https://doi.org/10.1002/pol.1979.170170603
Abstract
The kinetics of enantiomerically enriched t‐butyl thiirane was studied. The stereoelectivity and the kinetic behavior are not changed when a monomer of an initial enantiomeric composition lower than a defined limit value is used. When the enantiomeric composition is higher than this value, the stereoelectivity increases. In agreement with kinetic results, a mechanism is proposed involving, in a first step, the complexation of monomer on preexisting sites of the initiator with formation of highly selective chiral active species on which propagation occurs.Keywords
This publication has 3 references indexed in Scilit:
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- Polymerization of t‐butyl thiirane. I. Stereoelective polymerization of the racemic monomerJournal of Polymer Science: Polymer Chemistry Edition, 1979
- Alcoolyse et glycolyse de derives organozinciques et organocadmiens par des composes chirauxJournal of Organometallic Chemistry, 1974