A computational study of the radical ring-opening polymerization of diphosphetanes

Michelle L. Coote; Mansoor Namazian; S. Bruce Wild

doi:10.1071/CH10085

A computational study of the radical ring-opening polymerization of diphosphetanes

Michelle L. Coote, Mansoor Namazian, S. Bruce Wild

Research output: Contribution to journal › Article › peer-review

4 Citations (Scopus)

Abstract

Radical ring-opening of four-membered 1,3-diphosphetanes appears to be a facile process of similar propensity and mechanism to that of the parent phosphetanes, but the greater kinetic stability of the diphosphetanes could make them more attractive precursors for polymerization.

Original language	English
Pages (from-to)	1189-1194
Number of pages	6
Journal	Australian Journal of Chemistry
Volume	63
Issue number	8
DOIs	https://doi.org/10.1071/CH10085
Publication status	Published - 2010

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10.1071/CH10085

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title = "A computational study of the radical ring-opening polymerization of diphosphetanes",

abstract = "Radical ring-opening of four-membered 1,3-diphosphetanes appears to be a facile process of similar propensity and mechanism to that of the parent phosphetanes, but the greater kinetic stability of the diphosphetanes could make them more attractive precursors for polymerization.",

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AB - Radical ring-opening of four-membered 1,3-diphosphetanes appears to be a facile process of similar propensity and mechanism to that of the parent phosphetanes, but the greater kinetic stability of the diphosphetanes could make them more attractive precursors for polymerization.

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JO - Australian Journal of Chemistry

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A computational study of the radical ring-opening polymerization of diphosphetanes

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