The Effect of Tacticity on the Conformational Properties of Poly(1-olefin sulfone)s

Karl Malcolm, John Callan, Allan H. Fawcett

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

The effect of tacticity on the conformational properties of poly(olefin sulfone)s was studied. Tactic polymers, prepared from racemic thiirane monomers using chiral inititators were compared with atactic polymers prepared by free radical co-polymerisation of the 1-olefin with sulfur dioxide. Analysis of the XRD patterns showed that the tactic polymers formed more ordered structures in the bulk with longer layer spacings, consistent with a model in which their side chains meet at the tips in contrast with the atactic polymers whose side chains interdigitate. 13C MAS nmr experiments suggest that as tacticity increases so too does the proportion of C-S bonds in the gauche conformation, however the proportion of S-C bonds in the trans conformation falls, in contrast to a reported molecular mechanics study. Finally, DSC measurements on the polymers with longer side chains showed the presence of two endotherms on heating, illustrating definite liquid crystalline behaviour.
Original languageEnglish
Pages (from-to)107-113
Number of pages7
JournalJournal of polymer Research
Volume15 (2)
Issue number2
DOIs
Publication statusPublished - Apr 2008

ASJC Scopus subject areas

  • Materials Chemistry
  • Polymers and Plastics

Fingerprint Dive into the research topics of 'The Effect of Tacticity on the Conformational Properties of Poly(1-olefin sulfone)s'. Together they form a unique fingerprint.

  • Cite this