83291-39-8Relevant academic research and scientific papers
Regio- and Stereo-selectivity in the Hydrogenation of Aryl Phosphines by Niobium Aryloxide Compounds
Potyen, Mark C.,Rothwell, Ian P.
, p. 849 - 852 (1995)
The sequential hydrogenation of the three aryl rings in PPh3 by the catalyst system /3BunLi occurs with relative rates of 39:28:1; NMR analysis of the PhPCy2 obtained from and shows a predominantly all cis hydrogenation of both aryl rings has occurred.
A new synthetic route to ligands of the general composition R2PCH2ER′2 (E = P, As) and some rhodium complexes derived thereof
Wolf, Justin,Manger, Matthias,Schmidt, Ulrich,Fries, Guido,Barth, Dietmar,Weberndoerfer, Birgit,Vicic, David A.,Jones, William D.,Werner, Helmut
, p. 1867 - 1875 (2007/10/03)
Symmetrical and unsymmetrical bis(phosphino)methanes R2PCH2PR′2 (8-16) as well as the arsino(phosphino) analogues R′2AsCH2PR2 (21-25) with bulky alkyl, cycloalkyl or aryl groups R and R′ were prepared from the stannylated phosphines R2PCH2SnR″3 (3-5, 6, 7) Via metalation with MeLi or PhLi in the presence of tetramethylethylenediamine and subsequent treatment with R′2PCl or R′2AsCl, respectively. Compound 25 [R′ = Cy, R = (R)-menthyl] is the first arsino(phosphino)methane which has been structurally characterized. The bis(phosphino)methanes R2PCH2PR2 (R = Pri 17, Cy 18) and R2PCH2PR′2 (12, 19, 20) were also obtained by thermal reaction of R2PCH2SnPh3 and the corresponding chlorophosphine R2PCl or R′2PCl in the absence of solvent. The bis(cyclooctene) derivative [RhCl(C8H14)2]2 26 reacted with excess Pri2PCH2PPri2 to give [Rh(κ2P,P′-Pri2PCH 2PPri2)2]Cl 27, while treatment of 26 with Ph2PCH2PPri2 yielded the chloro-bridged dimer [RhCl(κ2P,P′-Ph2PCH2PPr i2)]2 28. The reaction of the cationic species [Rh(C8H14)2(OCMe2) 2]PF6 29 with Cy2PCH2PPri2 in benzene or toluene afforded the half-sandwich-type complexes [(η6-C6H6)Rh(κ 2,P′-Cy2PCH2PPri 2)]PF6 30, [(η6-C6H5CH3)Rh(κ 2P,P′-Cy2PCH2PPri 2)]PF6 31, of which the latter was characterized by X-ray crystallography.
