Chelating or bridging Pd(II) and Pt(II) metalloligands from the functional phosphine ligand N-(diphenylphosphino)-1,3,4-thiadiazol-2-amine. New heterometallic Pd(II)/Pt(II) and Pt(II)/Au(I) complexes

The reaction of two equivalents of the functional phosphine ligand N-(diphenylphosphino)-1,3,4-thiadiazol-2-amine Ph2PNHC=NNCHS (2) with PdCl2(NCPh)2] in the presence of NEt3 gives the neutral, P,N-chelated complex cis-Pd(Ph2PN=CNN=CHS)2] (Pd(2-H)2], 3b), which is analogous to the Pt(II) analogue cis-Pt (Ph2PN=CNN=CHS)2] (Pt(2-H)2], 3a) reported previously. These complexes function as chelating metalloligands when further coordinated to a metal through each of the CH-N atoms. In the resulting complexes, each endo-cyclic N donor of the thiadiazole rings is bonded to a different metal centre. Thus, the heterodinuclear palladium/platinum complexes cis-Pt(Ph2PN=CNN=CHS)2PdCl2](Pt(2-H)2·PdCl2], 4a) and cis-Pd(Ph2PN=CNN=CHS)2PtCl2](Pd(2-H)2·PtCl2], 4b) were obtained by reaction with PdCl2(NCPh)2] and PtCl2(NCPh)2], respectively. In contrast, reaction of 3a with AuCl(tht)] occurred instead at the P-bound N atom, and afforded the platinum/digold complex cis-Pt{Ph2PN(AuCl)=CNN=CHS}2] (Pt(2-H)2(AuCl)2], 5). For comparison, reaction of 4a with HBF4 yielded cis-Pt(Ph2PNH=CNN=CHS)2PdCl2](BF4)2(H24a](BF4)2, 6), in which the chelated PdCl2 moiety is retained. Complexes 3b, 4a·CH2Cl2, 4b·0.5C7H8, 5·4CHCl3 and 6 have been structurally characterized by X-ray diffraction.