Enantiomeric Resolution of Chiral Metallobis(porphyrin)s: Studies on Rotatability of Electronically Coupled Porphyrin Ligands

Authors


  • We thank Dr. N. Morisaki and Mr. J. Tsuchiya for HRMS and EPR measurements, respectively.

Abstract

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The porphyrin–prophyrin distance and the spatial requirements of the porphyrin substituents are parameters that influence the rotatability of the ligands in metal bis(porphyrinate)s (shown on the right): the chiral cerium complexes were much easier to racemize than the zirconium complexes. The porphyrin ligands in the latter rotate in response to H+.

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