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Application of NMR spectroscopy of chiral association complexes. 13—electron donor–acceptor complexes between racemic carbazolo[3,4-c]carbazoles and an optically active acceptor

✍ Scribed by Siddik İçli; Thomas Burgemeister; Albrecht Mannschreck; Maximilian Zander


Publisher
John Wiley and Sons
Year
1982
Tongue
English
Weight
432 KB
Volume
20
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

Strong electron donor–acceptor (EDA) association between carbazolo[3,4‐c]carbazoles and an optically active tetranitrofluorenone derivative was detected by UV–visible spectroscopy and by ^1^H NMR shifts. ^1^H NMR splittings at low temperatures are due to diastereomeric association complexes and, thus, prove the chirality of carbazolocarbazoles.