Synthesis, structure and spectroelectrochemistry of bis(η6-1,4-tri-tert-butyl-benzene)chromium(0) and bis(η5-1,2,4-tri-tert-butyl-cyclopentadienyl)cobalt(II). Dia- and paramagnetic sandwich complexes derived from sterically highly demanding π-ligands

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Abstract

Metal atom synthesis gives access to the bis(arene)chromium sandwich of 1,4 di-tert-butyl-benzene (5). 5 displays an axial sandwich structure with a linear arene-chromium-arene axis and a Cr-arene distance of 1.64 Å. Reduction of [{(η5-1,2,4 tri-tert-butyl-Cp)CoCl}2] with the trianion of decacyclene in THF produces the cobaltocene sandwich [(η5-1,2,4 tri-tert-butyl Cp)2Co] 2 as black crystals in 65% yield. Electrochemistry shows that the monocations 2+ and 5+ are able to support reversibly the one-electron reduction to their corresponding neutral congeners. © 1999 Elsevier Science S.A.

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Schneider, J. J., Czap, N., Spickermann, D., Lehmann, C. W., Fontani, M., Laschi, F., & Zanello, P. (1999). Synthesis, structure and spectroelectrochemistry of bis(η6-1,4-tri-tert-butyl-benzene)chromium(0) and bis(η5-1,2,4-tri-tert-butyl-cyclopentadienyl)cobalt(II). Dia- and paramagnetic sandwich complexes derived from sterically highly demanding π-ligands. Journal of Organometallic Chemistry, 590(1), 7–14. https://doi.org/10.1016/S0022-328X(99)00383-6

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