Preparation and reactivity of platinathiadiazetidine 1,1-dioxide and platinadiazaphosphetidine 2-oxide complexes
摘要:
Treatment of the complexes cis-[PtCl2L2] (L = donor ligand) with either N,N'-diphenylsulfamide or N,N',P-triphenylphosphonic diamide in the presence of an excess of silver(I) oxide in refluxing dichloromethane yielded the new metallacycles [activated Pt{NPhS(O)2NPh}L2] and [activated Pt{NPhP(O)(Ph)NPh}L2] respectively. The X-ray crystal structure of [activated Pt{NPhS(O)2NPh}(cod)] (cod = cycloocta-1,5-diene) showed the presence of an entirely flat four-membered ring, whereas that of [activated Pt{NPhP(O)(Ph)NPh}-(PPh3)2] exhibits a small puckering angle, but with no substantial Pt...P transannular interaction. tert-Butyl isocyanide displaces a phosphine ligand from [activated Pt{NPhS(O)2NPh}(PPh3)2].