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Synthesis of 5-arylpyrimidine-2-carboxylic acids and the liquid-crystal characteristics of their aryl esters

Journal Article · · Chem. Heterocycl. Compd. (Engl. Transl.); (United States)
DOI:https://doi.org/10.1007/BF00515002· OSTI ID:6290946
5-Arylpyrimidine-2-carboxylic acids were synthesized by the hydrolysis of 5-aryl-2-cyanopyrimidines and the oxidation of 5-aryl-2-styrylpyrimidines under the conditions of phase-transfer catalysis. The aryl esters of the acids were obtained, and their liquid-crystal characteristics were studied. The p-substituted aryl esters of 5-phenylpyrimidine-2-carboxylic acid do not exhibit mesomorphism, but the introduction of a butyloxy group at the p position of the phenyl residue leads to the appearance of nematic characteristics. Aryl 5-phenylpyrimidinylcarbonyloxy-benzoates are nematic liquid crystals with a thermally stable meso phase and an existence range of 50-80/sup 0/C.
Research Organization:
Novosibirsk Institute of Organic Chemistry, USSR
OSTI ID:
6290946
Journal Information:
Chem. Heterocycl. Compd. (Engl. Transl.); (United States), Journal Name: Chem. Heterocycl. Compd. (Engl. Transl.); (United States) Vol. 22:3; ISSN CHCCA
Country of Publication:
United States
Language:
English

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