Abstract
The influence of the nature of the metal (metallofragment) on the spin density distribution in radical anions ando-semiquinone metal complexes (derivatives of sterically hindered 5,5′-di-tert-butyl-2,2′-dimethylbiphenyl-3,4,3′,4′-diquinone) was studied by ESR spectroscopy. Despite the difference in the characters of the spin density distribution between the radical anion derivatives (M=Li, Na, K, and CoCp2) ando-semiquinone complexes (MLn=Tl, SnPh3, TlMe2, Cu(PPh3)2, Cu(CNR)2, and Mn(CO)4) in all cases significant delocalization of the spin density of an unpaired electron into theo-quinone ring is observed.
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Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 904–907, May, 1998.
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Abakumov, G.A., Cherkasov, V.K., Nevodchikov, V.I. et al. ESR study of radical anions ando-semiquinone metal complexes—5,5′-di-tert-butyl-2,2′-dimethylbiphenyl-3,4,3′,4′-diquinone derivatives. Russ Chem Bull 47, 875–878 (1998). https://doi.org/10.1007/BF02498155
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DOI: https://doi.org/10.1007/BF02498155