Issue 8, 1993

Synthesis, transition temperatures and optical anisotropy of some isothiocyanato-substituted biphenyls

Abstract

A range of alkyl-, alkoxy- and alkylsulfanyl-substituted biphenyls with terminal isothiocyanato substituents have been prepared and their suitability as dopants in nematic mixtures of high optical anisotropy evaluated. Palladium-catalysed cross-coupling reactions involving arylboronic acids have been used to synthesize the biphenyl core unit, followed by functional-group interconversions to give the desired isothiocyanato-substituted materials. The –NCS terminal group is in conjugation with the biphenyl core and this combination was expected to provide materials of high optical anisotropy. Mesogenic and optical properties have been determined and are discussed.

Article information

Article type
Paper

J. Mater. Chem., 1993,3, 851-859

Synthesis, transition temperatures and optical anisotropy of some isothiocyanato-substituted biphenyls

M. Hird, A. J. Seed, K. J. Toyne, J. W. Goodby, G. W. Gray and D. G. McDonnell, J. Mater. Chem., 1993, 3, 851 DOI: 10.1039/JM9930300851

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements