Polymerization of t‐butyl thiirane. II. Polymerization of enantiomerically enriched monomer. Mechanism of stereoelective process

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.

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