Journal of the Chemical Society. Perkin transactions II p. 465 - 472 (1982)
Update date:2022-08-05
Topics:
Behnam, Basil A.
Hall, D. Muriel
13 Azomethines have been prepared from 2-amino-9,10-dihydrophenanthrene by reaction with aromatic aldehydes.Those with p-alkoxy, p-cyano or p-phenyl substituents in the aldehydic ring have a nematic mesophase.U.v. spectra, 1H and 13C n.m.r. spectra, and mass spectra of the series are discussed.Mass spectra show that ortho-substituents in the aldehydic ring substantially modify the fragmentation pattern.
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Doi:10.1007/BF00506437
(1983)Doi:10.1246/bcsj.56.2527
(1983)Doi:10.1021/ja0470158
(2004)Doi:10.1016/j.tetasy.2004.11.023
(2004)Doi:10.1021/ml400462j
(2014)Doi:10.1021/ja01223a511
(1945)
