Arrested disproportionation in trivalent, mononuclear, and non-metallocene complexes of Zr(III) and Hf(III)

Grant LN, Miehlich M, Meyer K, Mindiola DJ (2018)


Publication Type: Journal article

Publication year: 2018

Journal

Book Volume: 54

Pages Range: 2052-2055

Journal Issue: 16

DOI: 10.1039/c7cc08815a

Abstract

Reduction of the group 4 transition metal precursors [(PN)2MCl2] (M = Zr (1), and Hf (2)); PN- = (N-(2-(diisopropylphosphino)-4-methylphenyl)-2,4,6-trimethylanilide), both readily prepared by transmetallation of 2 LiPN with [MCl4(THF)2], with a slight excess of KC8, resulted in the isolation of the trivalent complexes [(PN)2MCl] (M = Zr (3), and Hf (4)). Complexes 1-4 were all identified by solid-state X-ray diffraction analysis, whereas in the case of 3 and 4 low temperature X-band EPR spectroscopy allowed for the identification of these metal-centered d1 radicals. A comparison with the isostructural and isoelectronic but more stable [(PN)2TiCl] is also presented.

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APA:

Grant, L.N., Miehlich, M., Meyer, K., & Mindiola, D.J. (2018). Arrested disproportionation in trivalent, mononuclear, and non-metallocene complexes of Zr(III) and Hf(III). Chemical Communications, 54(16), 2052-2055. https://dx.doi.org/10.1039/c7cc08815a

MLA:

Grant, Lauren N., et al. "Arrested disproportionation in trivalent, mononuclear, and non-metallocene complexes of Zr(III) and Hf(III)." Chemical Communications 54.16 (2018): 2052-2055.

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