Manganese nitride complexes in oxidation states III, IV, and V: Synthesis and electronic structure

Kropp H, King AE, Khusniyarov M, Heinemann FW, Lancaster KM, Debeer S, Bill E, Meyer K (2012)


Publication Type: Journal article, Original article

Publication year: 2012

Journal

Original Authors: Kropp H., King A.E., Khusniyarov M.M., Heinemann F.W., Lancaster K.M., Debeer S., Bill E., Meyer K.

Publisher: American Chemical Society

Book Volume: 134

Pages Range: 15538-15544

Journal Issue: 37

DOI: 10.1021/ja306647c

Abstract

The synthesis and characterization of a series of manganese nitrides in a tripodal chelating tris(carbene) ligand framework is described. Photolysis of [(TIMEN)Mn(N)] (where TIMEN = tris[2-(3-xylylimidazol-2-ylidene)ethyl]amine) yields the isolable molecular Mn nitride, [(TIMEN)Mn(N)]. Spectroscopic and DFT studies indicate that this Mn d complex has a doublet electronic ground state. The metal-centered one-electron oxidation of this Mn species results in formation of the pentavalent Mn nitride, [(TIMEN)Mn(N)]. Unlike previously reported, tetragonal Mn nitrides with a d, nonmagnetic S = 0 ground state, this trigonal bipyramidal complex has a triplet ground state S = 1. One-electron reduction of [(TIMEN)Mn(N)] produces the neutral, nonmagnetic trivalent [(TIMEN )Mn(N)] species with a d low-spin, S = 0, ground state. © 2012 American Chemical Society.

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APA:

Kropp, H., King, A.E., Khusniyarov, M., Heinemann, F.W., Lancaster, K.M., Debeer, S.,... Meyer, K. (2012). Manganese nitride complexes in oxidation states III, IV, and V: Synthesis and electronic structure. Journal of the American Chemical Society, 134(37), 15538-15544. https://doi.org/10.1021/ja306647c

MLA:

Kropp, Henning, et al. "Manganese nitride complexes in oxidation states III, IV, and V: Synthesis and electronic structure." Journal of the American Chemical Society 134.37 (2012): 15538-15544.

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