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The chiral crown conformation in paddlewheel complexes.

ABSTRACT: Bimetallic paddlewheel complexes derived from imides of (S)-tert-leucine adopt 'chiral crown' configurations in which the four imide groups are projected in a chiral arrangement on one face, and the four tert-butyl groups are projected on the opposite face. In this contribution, the generality of the chiral crown conformation is examined through crystallographic studies where the metal and the nature of the chiral ligands are altered. Based upon these observations, a model is proposed to explain the factors which create bias for the chiral crown configuration.

SUBMITTER: DeAngelis A

PROVIDER: S-EPMC3908875 | biostudies-literature | 2010 Jul

REPOSITORIES: biostudies-literature

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The chiral crown conformation in paddlewheel complexes.

DeAngelis Andrew A Boruta David T DT Lubin Jean-Bernard JB Plampin James N JN Yap Glenn P A GP Fox Joseph M JM

Chemical communications (Cambridge, England) 20100511 25

Bimetallic paddlewheel complexes derived from imides of (S)-tert-leucine adopt 'chiral crown' configurations in which the four imide groups are projected in a chiral arrangement on one face, and the four tert-butyl groups are projected on the opposite face. In this contribution, the generality of the chiral crown conformation is examined through crystallographic studies where the metal and the nature of the chiral ligands are altered. Based upon these observations, a model is proposed to explain ...[more]

PMID: 20458417

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