PALLADIUM-COPPER CATALYZED COUPLING OF IRON SIGMA-METALLA-ALKYNES WITH ARYL HALIDES - A SIMPLE WAY TO LINK ELECTROACTIVE ORGANOIRON COMPLEXES WITH AROMATIC STRUCTURES
R. Denis et al., PALLADIUM-COPPER CATALYZED COUPLING OF IRON SIGMA-METALLA-ALKYNES WITH ARYL HALIDES - A SIMPLE WAY TO LINK ELECTROACTIVE ORGANOIRON COMPLEXES WITH AROMATIC STRUCTURES, Journal of organometallic chemistry, 546, 1997, pp. 615-618
In the presence of catalytic amounts of bis(triphenylphosphine)dichlor
opalladium(II) [(Ph3P)(2)PdCl2] and copper iodide (CuI) in di-iso-prop
ylamine, the terminal iron acetylide complex 1 [(Cp)(dppe)Fe(C=CH)] (
dppe = 1,2-bis(diphenylphosphino)ethane) can be coupled with various p
ara- or meta-substituted aryl bromides or iodides 2a-g to give the cor
responding functionalized complexes 3a-g [(Cp)(dppe)Fe(C=C-C6H4-G)] w
ith fair yields (G = NO2, CN, H, Br, Bu-t, OMe). (C) 1997 Elsevier Sci
ence S.A.