Issue 5, 1994

Redox-linked pyrrole NH deprotonation in a dicopper azacryptate system

Abstract

The pyrrole-based cryptand L, has asymmetric conformation when coordinated to dicopper(I); one-electron oxidation yields a localized mixed-valence dicopper cryptate of the singly deprotonated ligand and two-electron oxidation a dicopper(II) cryptate of the triply deprotonated ligand; single crystal X-ray structure determination shows two different irregular sites for CuII.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 649-651

Redox-linked pyrrole NH deprotonation in a dicopper azacryptate system

Q. Lu, V. McKee and J. Nelson, J. Chem. Soc., Chem. Commun., 1994, 649 DOI: 10.1039/C39940000649

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