The Full d3-d5Redox Series of Mononuclear Manganese Complexes: Geometries and Electronic Structures of [Mn(dgpy)2]n+

East NR, Forster C, Carrella LM, Rentschler E, Heinze K (2022)


Publication Type: Journal article

Publication year: 2022

Journal

Book Volume: 61

Pages Range: 14616-14625

Journal Issue: 37

DOI: 10.1021/acs.inorgchem.2c01680

Abstract

Although manganese ions exhibit a rich redox chemistry, redox processes are often accompanied by structural reorganization and a high propensity for ligand substitution, so that no complete structurally characterized manganese(II,III,IV) complex series without significant ligand sphere reorganization akin to the manganese(II,III,IV) oxides exists. We present here the series of pseudo-octahedral homoleptic manganese complexes [Mn(dgpy)2]n+(n = 2-4) with the adaptable tridentate push-pull ligand 2,6-diguanidylpyridine (dgpy). Mn-N bond lengths and N-Mn-N bond angles change characteristically from n = 2 to n = 4, while the overall [MnN6] coordination sphere is preserved. The manganese(III) complex [Mn(dgpy)2]3+exhibits a Jahn-Teller elongated octahedron and a negative D = -3.84 cm-1. Concomitantly with the consecutive oxidation of [Mn(dgpy)2]2+to [Mn(dgpy)2]4+, the optical properties evolve with increasing ligand-to-metal charge transfer character of the absorption bands culminating in the panchromatic absorption of the purple-black manganese(IV) complex [Mn(dgpy)2]4+

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How to cite

APA:

East, N.R., Forster, C., Carrella, L.M., Rentschler, E., & Heinze, K. (2022). The Full d3-d5Redox Series of Mononuclear Manganese Complexes: Geometries and Electronic Structures of [Mn(dgpy)2]n+. Inorganic Chemistry, 61(37), 14616-14625. https://dx.doi.org/10.1021/acs.inorgchem.2c01680

MLA:

East, Nathan R., et al. "The Full d3-d5Redox Series of Mononuclear Manganese Complexes: Geometries and Electronic Structures of [Mn(dgpy)2]n+." Inorganic Chemistry 61.37 (2022): 14616-14625.

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