Reactions of π-cyclopentadienyltriphenylphosphinemetal diiodides and π-cyclopentadienylcarbonylmetal diiodides (M = Co,Rh, Ir) with 1,4-dilithio-1,2,3,4-tetraphenylbutadiene |
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Authors: | Sylvia A. Gardner Marvin D. Rausch |
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Affiliation: | Department of Chemistry, University of Massachusetts, Amherst, Massachusetts 01002 U.S.A. |
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Abstract: | Reactions between π-cyclopentadienyltriphenylphosphinemetàl diiodides (M = Rh and Ir) and 1,4-dilithio-l,2,3,4-tetraphenylbutadiene result in the formation of 1-(π-cyclopentadienyl)-l-triphenylphosphine-2,3,4,5-tetraphenylrhodole and 1-(π-cyclopentadienyl)-1-triphenylphosphine-2,3,4,5-tetraphenyliridole, respectively, in low yield. Reactions between π-cyclopentadienyltriphenylphosphinecobalt diiodide or π-cyclopentadienylcarbonylcobalt diiodide do not produce the expected cobaltacyclopentadiene complexes, but instead a low yield of π-cyclopentadienyl-(π-tetraphenylcyclobutadiene)cobalt. The trimeric rhodium complex (π-C5H5Rh)3(CO)(PhCCPh) has been isolated from a reaction between 1,4-dilithio-l,2,3,4-tetraphenylbutadiene and π-cyclopentadienylcarbonylrhodium diiodide. The importance of metallocyclic intermediates in the formation of polynuclear complexes of this type is discussed. |
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Keywords: | Address correspondence to this author Alfred P. Sloan Foundation Fellow 1972–1974. |
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