ARYLMAGNESIUM TO ARYLCOPPER CONVERSION MONITORED BY SOLID-STATE CHARACTERIZATION OF HALIDE INTERMEDIATES - SYNTHESIS OF HOMOLEPTIC (O-VINYLPHENYL)COPPER
H. Eriksson et al., ARYLMAGNESIUM TO ARYLCOPPER CONVERSION MONITORED BY SOLID-STATE CHARACTERIZATION OF HALIDE INTERMEDIATES - SYNTHESIS OF HOMOLEPTIC (O-VINYLPHENYL)COPPER, Organometallics, 15(22), 1996, pp. 4823-4831
The reaction between Mg(viph)(2) (viph = o-vinylphenyl) and copper(I)
chloride has been found to be the best way of preparing the homoleptic
tetramer [Cu-4(viph)(4)]. The MgR(2) reagent crystallizes as monomeri
c [Mg(THF)(2)(viph)(2)] from a THF solution. In the reaction between t
he Grignard reagent (viph)MgBr and copper(I) chloride, two unstable mi
xed halide/aryl intermediates, [Mg(THF)(6)][Cu-5(viph)(2)Br-4](2) . TH
F (3) and [Mg(THF)(5)Cl][Cu-5(viph)(4)Br-2].-THF (4), were isolated an
d found to reduce the yield of [Cu-4(viph)(4)] markedly. The crystal s
tructures of 3 and 4 were determined and were found to exhibit unusual
coordination geometries for copper(I) and provide mechanistic informa
tion. Compound 3 was found to react with excess triphenylphosphine in
THF, yielding [Cu(PPh(3))(3)Br]. THF. It is suggested that [Cu-4(viph)
(4)], which is not pi-coordinated in the solid state or in THF solutio
n, may have important precursor qualities for the preparation of new o
rganocopper compounds.