Ternary complexes of palladium(II) containing (Te,S) and (Te,N) hybrid organotellurium ligands: synthesis, spectra and cis-trans isomeric conversion
摘要:
Five ternary complexes of palladium(II) namely [Pd(L(1))(2)](ClO4)(2) (1), [Pd(L(1))(L(2))](ClO4)(2) (2), [(PPh(3))(2)Pd(L(1))](ClO4)(2) (3), [(DppE)Pd(L(2))](ClO4)(2) (4) and [Pd(L(1))(L(3))](ClO4)(2) (5) where L(1) = MeSCH(2)CH(2)TeAr, L(2) = Me(2)NCH(2)CH(2)TeAr (Ar = 4-MeOC(6)H(4)) and L(3) = MeSCH(2)CH(OH)CH(2)SMe were synthesized by treating [PdCl2 . (L(1))] or [(PPh(3))(2)/(DPPE)PdCl2)] with AgClO4 and the appropriate ligand. The ligands L(1), L(2) and L(3) in these complexes are judged to be coordinated in bidentate mode on the basis of (1)HNMR and IR spectral data. All the complexes behave as 1:2 electrolytes in CH3CN. The Te-125(H-1) NMR spectra of 1 and 2 indicate that the ligands L(1) and L(2) in them are in a cis disposition in fleshly prepared dimethylsulphoxide-d(6)-CD3CN solutions, implying a similar configuration in the solid state but within a few hours there is partial conversion into the trans isomer.