Issue 36, 2020

A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange

Abstract

Successive chemical reductions of the heteroleptic complex [(tpy)CrIII(tphz)]3+ (tpy = terpyridine; tphz = tetrapyridophenazine) give rise to the mono- and di-radical redox isomers, [(tpy)CrIII(tphz˙)]2+ and [(tpy˙)CrIII(tphz˙)]+, respectively. As designed, the optimized overlap of the involved magnetic orbitals leads to extremely strong magnetic interactions between the S = 3/2 metal ion and S = 1/2 radical spins, affording well isolated ST = 1 and ST = 1/2 ground states at room temperature.

Graphical abstract: A heteroleptic diradical Cr(iii) complex with extended spin delocalization and large intramolecular magnetic exchange

Supplementary files

Article information

Article type
Communication
Submitted
20 Jan 2020
Accepted
19 Mar 2020
First published
24 Mar 2020

Chem. Commun., 2020,56, 4906-4909

A heteroleptic diradical Cr(III) complex with extended spin delocalization and large intramolecular magnetic exchange

X. Ma, E. A. Suturina, M. Rouzières, F. Wilhelm, A. Rogalev, R. Clérac and P. Dechambenoit, Chem. Commun., 2020, 56, 4906 DOI: 10.1039/D0CC00548G

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