Abstract
The syntheses and transition temperatures of 2-(4-butylsulphanylphenyl)-6-isothiocyanatonaphthalene and 1-(4-butylsulphanylphenyl)-2-(6-isothiocyanato-2-naphthyl)ethyne are reported and discussed. These are the first examples of mesogenic isothiocyanatonaphthalenes to be reported in the literature. The transition temperatures of these compounds were compared and contrasted with compounds where the naphthalene and benzene rings had been interchanged and the analogous compounds where a cyano group replaced the isothiocyanate. The new compounds had high nematic phase thermal stabilities and relatively low melting points. As part of this work we present a new synthetic method for the synthesis of the key 2-alkylsulphanyl-6-bromonaphthalene building block that is a marked improvement over currently available methodology.
Acknowledgements
The authors would like to express their gratitude to Dr Mahinda Gangoda for assistance in obtaining the NMR spectra and to Professor Robert J. Twieg for the generous use of the DSC instrument. This work was carried out with generous funding from Hughes Research Laboratories and Kent State University.