RESUMO
ion of chloride from [W(CO)5{PPhCl2}] with AgOSO2CF3 leads to the phosphine triflate complex [W(CO)5{PPhCl(OSO2CF3)}] which undergoes electrophilic substitution reactions with N,N-diethylaniline, anisole, N,N-dimethyl-p-toluidine, toluene, biphenyl, naphthalene, 2,7,9,9-tetramethyl xanthene, and allyltrimethylsilane to form the chlorophosphine complexes [W(CO)5{PPhClR}], where R = p-diethylanilinyl, p-anisyl, 2-(N,N-dimethyl-4-methylphenyl), p-tolyl, p-phenylphenyl, 1-naphthyl, 4-(2,7,9,9-tetramethylxanthyl), and allyl. Abstraction of the second chloride with AgOSO2CF3 leads, in most cases, to the respective phosphine triflates [W(CO)5{PPhR(OSO2CF3)}], which react with ferrocene to form the ferrocenyl phosphine complexes [W(CO)5{PPhR(C10H9Fe)}]. The W(CO)5 unit can be removed via photolysis in the presence of bis(diphenylphosphino)ethane to form metal-free phosphines.
RESUMO
In the presence of chloride abstractors, metal-coordinated chlorophosphines undergo facile room-temperature electrophilic substitution reactions with unsaturated organic substrates, leading to P-C bond formation. This methodology can be applied sequentially two or three times, stepwise or in one-pot reactions, to form phosphines with three different substituents. The reactions are rapid and high-yielding, and can be applied to a wide range of organic substrates, making them valuable tools for P-C bond formation.
