Two Diastereomeric Oxalatobis(S-butane-1,3-diamine)cobalt(III) Complexes

Abstract
A study of the oxalatobis(S-butane-1,3-diamine)cobalt(III) system shows that the dissymmetric ligand imposes uniquely related geometric and configurational selectivity. The selectivity is in agreement with conformational prediction and the magnitudes of the Cotton effects lend some support to recently developed sector rules.

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