Abstract

A new homologous series (ten compounds) of 2-hydroxy azo compounds SRn (where n:1–10) were synthesized. Their structures were elucidated using spectroscopic techniques such as IR (Infrared), 1H-NMR as well as elemental analysis. Mesomorphic properties and phase transitions were studied using polarized hot stage optical microscopy and differential scanning calorimetry (DSC), and are discussed as a function of the number of carbon atoms in the thioalkyl chain. It has been found that all compounds in the series are pure nematogens.

Highlights

  • IntroductionLiquid crystalline materials are of great interest for materials science as well as for life science

  • Liquid crystalline materials are of great interest for materials science as well as for life science.Their properties can be tuned by appropriate molecular design

  • A literature survey indicates that liquid crystalline azo esters with thioalkyl chains comprising different kinds of terminal groups are very rare, so, in the present work, we have prepared ten members (Figure 1) of homologous series of (SRn) in order to establish the effect of introducing sulfur atom instead of oxygen atom with the increase in the terminal thioalkyl chain on liquid crystalline properties

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Summary

Introduction

Liquid crystalline materials are of great interest for materials science as well as for life science Their properties can be tuned by appropriate molecular design. It is well known that the mesomorphic properties of calamitic liquid crystals can largely be influenced by the structural variation in terminal substituents, like alkyl, alkyloxy and thioalkyl groups [1,2,3,4,5]. This can influence the melting points and mesophase types, etc. A literature survey indicates that liquid crystalline azo esters with thioalkyl chains comprising different kinds of terminal groups are very rare, so, in the present work, we have prepared ten members (Figure 1) of homologous series of (SRn) in order to establish the effect of introducing sulfur atom instead of oxygen atom with the increase in the terminal thioalkyl chain on liquid crystalline properties

Result and Discussion
General
Diazotization of p-Toluidine
Coupling with Phenol
Synthesis of Esters E-SRn
Conclusions
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