Optically active polyamidoimides based on amino acids containing cyclohexane fragment

Optically active polyamidoimides based on amino acids containing cyclohexane fragment New amino carboxylic acids containing a cyclohexane fragment and an L-leucine or L-valine fragment were synthesized. The reactions of the synthesized amino acids with 4,4′-oxydiphthalic anhydride gave in quantitative yields the dicarboxylic acids, which were converted to the corresponding dichlorides. Low-temperature polycondensation of the synthesized dichlorides with 4,4′-diaminodiphenyl ether yielded optically active polyamidoimides, which are soluble in various organic solvents and exhibit enhanced heat resistance. The structures of the synthesized monomeric compounds and polymers were confirmed by elemental analysis, IR and 1H NMR spectroscopy, and high-resolution mass spectrometry. Specific rotation angles of the synthesized amino carboxylic acids and polyamidoimides were determined. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Russian Journal of Applied Chemistry Springer Journals

Optically active polyamidoimides based on amino acids containing cyclohexane fragment

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Publisher
Pleiades Publishing
Copyright
Copyright © 2015 by Pleiades Publishing, Ltd.
Subject
Chemistry; Chemistry/Food Science, general; Industrial Chemistry/Chemical Engineering
ISSN
1070-4272
eISSN
1608-3296
D.O.I.
10.1134/S1070427215100171
Publisher site
See Article on Publisher Site

Abstract

New amino carboxylic acids containing a cyclohexane fragment and an L-leucine or L-valine fragment were synthesized. The reactions of the synthesized amino acids with 4,4′-oxydiphthalic anhydride gave in quantitative yields the dicarboxylic acids, which were converted to the corresponding dichlorides. Low-temperature polycondensation of the synthesized dichlorides with 4,4′-diaminodiphenyl ether yielded optically active polyamidoimides, which are soluble in various organic solvents and exhibit enhanced heat resistance. The structures of the synthesized monomeric compounds and polymers were confirmed by elemental analysis, IR and 1H NMR spectroscopy, and high-resolution mass spectrometry. Specific rotation angles of the synthesized amino carboxylic acids and polyamidoimides were determined.

Journal

Russian Journal of Applied ChemistrySpringer Journals

Published: Jan 31, 2016

References

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