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Chiral C and S conformers of aromatic diimide triads
Author(s) -
Gawroński J.,
Gawrońska K.,
Kacprzak K.
Publication year - 2001
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/chir.1038
Subject(s) - chemistry , conformational isomerism , diimide , chirality (physics) , moiety , circular dichroism , stereochemistry , molecule , asymmetric carbon , crystallography , perylene , organic chemistry , chiral symmetry , physics , optically active , quantum mechanics , nambu–jona lasinio model , quark
Chiral triads composed of a central aromatic diimide moiety and two outer aromatic molecules connected by one‐ or two‐carbon linkers exist in an equilibrium of C and S conformers, as inferred from analysis of circular dichroism and nuclear magnetic resonance spectra, as well as from molecular modeling. Chirality 13:322–328, 2001. © 2001 Wiley‐Liss, Inc.