4.5 Article

Weak absolute helicity direction in Ni-salen by trans-cyclohexane-(1R,2R)-diamine

Journal

INORGANICA CHIMICA ACTA
Volume 364, Issue 1, Pages 259-260

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ica.2010.07.044

Keywords

Absolute helicity; Salen; Ni Catalyst; Enantioselective; Cyclohexane-diamine; Crystal structure

Funding

  1. NSF [CHE-0547865, CHE 0840401]

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Helical Ni-salen foldamers were synthesized from enantiomerically pure cyclohexane-(1R,2R)-diamine, N, N'-bis-(N-phenyl (4-diphenylphosphine)-3-salicylidenato carboxamide)-(1R,2R)-cyclohexanediamina-to-nickel(II). X-ray structural characterization of the absolute helicities observed confirms our earlier assertions, based on solution spectroscopic evidence, that trans-cyclohexane-diamine, a common component of chiral salen catalysts, is a weak director of absolute helicity for Ni-salen. (C) 2010 Elsevier B. V. All rights reserved.

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