S-Cholesteryl Alkanethioates

Abstract

A homologous series of S-cholesteryl alkanethioates was prepared by reaction of 3beta-mercaptocholest-5-ene with the imidazolides of alkanoic acids. The mesomorphic properties of 20 members, S-cholesteryl thioformate through eicosanethioate were determined. All alkanethioates are monotropic cholesteric except the cholesteryl thioformate. Cholesteryl thioheptanoate and all higher homologues in this series also exhibit a monotropic smectic mesophase. A comparison with the corresponding cholesteryl alkanoates shows that the replacement of the ester group by the thiol ester group leads to an increase in both the smectic-cholesteric and the cholesteric-isotropic transition temperatures.

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Document Details

Document Type
Technical Report
Publication Date
Jul 13, 1970
Accession Number
AD0754466

Entities

People

  • Juergen L. W. Pohlmann
  • Phillip R. Boyd
  • Wolfgang Elser

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  • Chemistry

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