4.5 Article

Synthesis and Characterization of a Cobalt(III) Corrole with an S-Bound DMSO Ligand

Journal

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Volume 2021, Issue 35, Pages 3540-3548

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.202100524

Keywords

Ab initio calculations; Cobalt; Corrole; DMSO; Innocent

Funding

  1. Alexander von Humboldt Foundation
  2. University of Stuttgart
  3. ASACTEI, Provincia de Santa Fe, Argentina
  4. Projekt DEAL

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A low-spin Co(III) complex with an S-bound dimethylsulfoxide (DMSO) ligand was synthesized, and its coordination mode was determined for the first time through X-ray diffraction. Spectral data indicated that the DMSO ligand remains bound in solution, and calculations showed the influence of the S atom on the electronic structure and spin configuration of the complex.
We have synthesized a low-spin Co(III) complex of 5,15-bis(4-nitrophenyl)-10-(2-methylcarboxyphenyl)corrole with an S-bound dimethylsulfoxide (DMSO) ligand (1DMSO) and determined the coordination mode through X-ray diffraction for the first time. UV-vis-NIR spectral data show that the DMSO ligand does not dissociate in MeCN solution, and EPR results indicate that the first oxidation is ligand centered and suggest that not only DMSO remains bound but a second apical ligand, possibly MeCN, binds to the cobalt center. Multiconfigurational wavefunction electronic structure methods (CASSCF/NEVPT2) allowed us to determine that in the neutral complex the corrole behaves as an innocent trianionic ligand and that the sigma-donor effect of the S atom determines the low-spin configuration by raising the energy of the Co 3dz(2) orbital. While DFT calculations predict a ground open-shell singlet for both S-bound and O-bound DMSO variants, CASSCF/NEVPT2 calculations predict a closed-shell singlet ground state in both cases. These calculations reproduce considerably well the UV-vis-NIR spectrum of 1DMSO in solution, validating the closed-shell singlet description.

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