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.
Russian Journal of Applied Chemistry – Springer Journals
Published: Jan 31, 2016
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