NMR study of mononuclear, binuclear and trinuclear tris(hydroxymethyl)phosphine-platinum(II) complexes with aquo or hydroxo ligands
作者:Emiliana Costa、Martin Murray、Paul G. Pringle、Martin B. Smith
DOI:10.1016/s0020-1693(00)83810-4
日期:1993.11
Treatment of [PtX(2)P(CH2OH)(3)}(2)] (X=Cl or Br) with AgY (Y=NO3, BF4, PF6 or ClO4,) in water gives three species A, B and C. Addition of HY to this mixture gives A exclusively which is identified as the bis(aquo) cation [Pt(OH2)(2)P(CH2OH)(3)}(2)](2+). The aquo ligands can be substituted by pyridine, 2,2'-bipyridine or 9,10-phenanthroline to give the corresponding [PtL(2)P(CH2OH)(3)}(2)](2+). Treatment of [Pt(OH2)(2)P(CH2OH)(3)}(2)](2+) with NEt(3), gives B which is identified as the binuclear species [Pt-2(mu-OH)(2)P(CH2OH)(3)}(4)](2+). After 24 h in acid solution in the presence of Ag+, the third species C is the main product which is trinuclear (as evidenced by P-31 and Pt-195 NMR spectroscopy) and is assigned the structure [Pt-3(mu-OH)(3)P(CH2OH)(3)}(6)](3+). The products are very soluble in water and have been characterised only by P-31 and Pt-195 NMR spectroscopy. The chemistry of these P(CH2OH)(3) complexes is compared with the chemistry of the analogous PMe(3), complexes.