Abstract
Complexes of the type [Rh(diolefin)(μ-X)]2 [X = Cl or Br; diolefin = cod (cycloocta-1,5-diene) or nbd (norbornadiene)] undergo dihalobridge cleavage with 2-substituted benzimidazoles to produce mononuclear complexes, RhX(diolefin)(R-BzlH) (R = α-Py or Ph), and N-heterocycle bridged dimers, [RhX(diolefin)]2(μ-N–N) (N–N = β-PyBzlH or γ-PyBzlH). Facile replacement ofone or both diolefins by CO occurs in the products to yield the corresponding di/tetracarbonyl complexes. Probable structures have been proposed for the complexes on the basis of physical, i.r., far-i.r. and 1H- and 13C-n.m.r. spectral techniques and FAB-MS.
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Gayathri, V., Leelamani, E.G., Gowda, N.M.N. et al. Organo-rhodium(I) complexes containing mono and bidentate N-heterocycles. Transition Metal Chemistry 25, 450–455 (2000). https://doi.org/10.1023/A:1007046228629
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DOI: https://doi.org/10.1023/A:1007046228629