<link rel="stylesheet" href="styles.cf390c6bfbe7555f.css"> Skip to main content

Synthesis and mesomorphic properties of Schiff base esters possessing terminal chloro substituent

Loading...
Thumbnail Image

Journal Title

Journal ISSN

Volume Title

Publisher

DOI

10.1016/j.cclet.2010.01.023

Abstract

A homologous series of Schiff base esters, 4-chlorobenzylidene-4'-n-alkanoyloxyanilines, containing even number of carbons at the end groups of the molecules (C(n-1)H(2n-1)COO-, n = 4, 6, 8, 10, 12, 14, 16) were synthesized. The mesomorphic properties were investigated by differential scanning calorimetry (DSC) and polarizing optical microscopy (POM). It was found that the end groups of the molecules had an effect on the mesomorphic properties. n-Butanoyloxy was found non-mesogenic, whilst n-hexanoyloxy exhibited monotropic smectic phase. The higher members in this homologous series were enantiotropic smectogens. (C) 2010 Sie Tiong Ha. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

Description

Citation

Endorsement

Review

Supplemented By

Referenced By