70530-40-4Relevant academic research and scientific papers
Influence of aromatic ring substituents and co-ligand on the binding mode of a phosphine-borane-stabilized carbanion; crystal structures of [[(Me3Si)2{Ph2P(BH3)}C]KLn]2[Ln = (OEt
Izod, Keith,Wills, Corinne,Clegg, William,Harrington, Ross W.
, p. 5060 - 5064 (2007)
The phosphine-borane adduct (Me3Si)2CHPPh2(BH3) (1) is readily prepared from the reaction between (Me3Si)2CHPCl2 and 2 equiv of PhMgBr in refluxing THF, followed by treatment wit
Desilylation and cyclometallation reactions of diphenylphosphine with platinum(II) compounds. Crystal structure of trans->
Al-Juaid, Salih S.,Eaborn, Colin,Hitchock, Peter B.,Smith, J. David,Zanotto, Livio,Kapoor, Pramesh N.
, p. 69 - 75 (2007/10/02)
The yellow complex trans- (L = PPh2CH(SiMe3)2) has been characterised.At attempt to make a similar complex with the more sterically hindered phosphine PPh2C(SiMe3)3 resulted in the loss of a trimethylsilyl group from one phosphine ligand and activation of a C-H bond in another to give the white complex , the structure of which was established by X-ray diffraction.
Ambivalent Reactions of Phosphanes Metallated in α-Position with n-Butyllithium
Appel, Rolf,Haubrich, Gerhard,Knoch, Falk
, p. 2063 - 2075 (2007/10/02)
The reaction of diphenyl(trimethylsilylmethyl)phosphane (1) with n-butyllithium yields the lithium methanide 2, which reacts with chlorotrimethylsilane to form diphenylphosphane (3).Repeated lithiation yields the ambivalent inte
Some phosphorus Derivatives
Eaborn, Colin,Retta, Negussie,Smith, J. David
, p. 905 - 910 (2007/10/02)
Treatment of Li with PPh2Cl gave the phosphine PPh2, which, in spite of the steric crowding caused by the silicon ligand, was readily converted into the phosphonium salts Ph2H>I and Ph2Me>I; the latter on heating gave the ylid MePh2PC(SiMe3)2.In methanol at room temperature the phosphine PPh2 readily loses one Me3Si group to give PPh2; the remaining Me3Si groups are lost successively, with decreasing ease, giving finally PPh2Me.These Si-C bond cleavages are catalysed by acid but inhibited by base, and it is suggested that the initial step is protonation of the phosphine.The quaternary salt Ph2Me>I successively loses its Me3Si groups very readily in methanol, ultimately to give I.
