Chiral  C  and  S  conformers of aromatic diimide triads | Zendy

Gawroński J. | Zendy; Gawrońska K. | Zendy; Kacprzak K. | Zendy

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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.

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