Issue 15, 2024

Phenoxazinyl Zn(ii) diradical complex formed via redox-driven cyclization of a 2-aminophenol-based N3O ligand. Isolation of the modified N3 ligand radical and its Ni(ii) complex

Abstract

Aerobic reaction between the pyridine-2-carboxamide-2-aminophenol N3O ligand (H3L1) and Zn(ClO4)2·6H2O in CH3CN affords an N3 phenoxazinylate coordinated Zn(II) complex; its diradical electronic structure [ZnII{(L1*)˙}2] has been elucidated from redox, spectroscopic (UV-VIS and EPR), and magnetic measurements and DFT calculations. Isolation and characterization of the metal-assisted redox-driven modified N3 ligand as a radical cation (H2L1*)˙+ and its Ni(II)-diradical complex [NiII{(L1*)˙}2] have also been achieved.

Graphical abstract: Phenoxazinyl Zn(ii) diradical complex formed via redox-driven cyclization of a 2-aminophenol-based N3O ligand. Isolation of the modified N3 ligand radical and its Ni(ii) complex

Supplementary files

Article information

Article type
Communication
Submitted
07 Feb 2024
Accepted
18 Mar 2024
First published
02 Apr 2024

Dalton Trans., 2024,53, 6515-6519

Phenoxazinyl Zn(II) diradical complex formed via redox-driven cyclization of a 2-aminophenol-based N3O ligand. Isolation of the modified N3 ligand radical and its Ni(II) complex

N. Mukhopadhyay, A. Sengupta, F. Lloret and R. Mukherjee, Dalton Trans., 2024, 53, 6515 DOI: 10.1039/D4DT00374H

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