Redox properties of bis-cobalt(III) complex of 3,3′-linked N-confused porphyrin dimer with axial pyridine ligands

Author:

Iwanaga Osamu1,Yoshida Naoya1,Miyazaki Takaaki2,Tani Fumito3,Mori Shigeki4,Shimizu Soji1,Ishida Masatoshi5,Furuta Hiroyuki16

Affiliation:

1. Department of Applied Chemistry, Graduate School of Engineering, Kyushu University, Fukuoka 819-0395, Japan

2. Department of Chemistry, Faculty of Science, Fukuoka University, Fukuoka 814-0180, Japan

3. Institute for Materials Chemistry and Engineering, Kyushu University, Fukuoka 819-0395, Japan

4. Advanced Research Support Center, Ehime University, Matsuyama 790-8577, Japan

5. Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Hachioji 192-0397, Japan

6. Research Organization of Science and Technology, Ritsumeikan University, Kusatsu 525-8577, Japan

Abstract

Novel cobalt(III) complexes of N-confused porphyrin (5,10,15,20-tetrakis(penta-fluorophenyl)-2-aza-21-carbaporphyrin) and its 3,3[Formula: see text]-linked dimer, Co1 and Co2, were synthesized and their structures were elucidated by X-ray crystallographic analysis and NMR spectroscopy. The redox properties of the complexes were examined by electrochemical approaches, and the corresponding oxidized/reduced species were analyzed by spectroelectrochemistry and DFT calculations. Notably, due to the facile redox feature of the N-confused porphyrins, ligand-centered oxidative/reductive processes were assumed for Co1 and Co2 presumably as inferred from the spectral analyses. These results indicate the unique multi-electron reservoir capability of the metal complexes of the N-confused porphyrin dimer.

Funder

Japan Society for the Promotion of Science

JST PREST

Encouraging Young Scientists Research Fund

JST SPRING

Publisher

World Scientific Pub Co Pte Ltd

Subject

General Chemistry

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