Synthesis and liquid crystal properties of substituted 5-(arylcarbonyloxy)-2-(<i>p</i>-cyanophenyl)pyrimidines

Authors

  • М. А. Михалева Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090
  • Г. А. Игонина Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090
  • B. А. Савельeв Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090

Abstract

Liquid crystal p-substituted benzoates, biphenylcarboxylates, and benzoyloxybenzoates were obtained on the basis of 5-hydroxy-2-(p-cyanophenyl)pyrimidine. The development of nematogenicity by the esters due to the p-cyanophenyl grouping was noted, and the appearance of the smectic mesophase by the variation of the ring framework of the acid fragment of the molecule was investigated.

How to Cite
Mikhaleva, M. A.; Igonina, G. A.; Savel'ev, V. A. Chem. Heterocycl. Compd. 1995, 31, 320. [Khim. Geterotsikl. Soedin. 1995, 371.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01373550

Downloads

Published

1995-03-25

Issue

No. 3 (1995)

Section

Original Papers