A sulfur monoxide complex of platinum fluoride with a positively charged ligand

A sulfur monoxide complex of platinum fluoride in the form of PtF(2)(η(1)-SO) was generated via the isomerization of a molecular complex Pt(SOF(2)) in cryogenic matrixes under UV-vis irradiation. The infrared absorptions observed at 1205.4, 619.8 and 594.9 cm(−1) are assigned to the S–O, antisymmetric and symmetric F–Pt–F stretching vibrations of the PtF(2)(η(1)-SO) complex, which possesses nonplanar C(s) symmetry with a singlet ground state according to density functional theory calculations. The experimental vibrational frequency and computed distance (1.449 Å) of the SO ligand indicate that the SO ligand features a positively charged character, which is further confirmed by natural bond orbital analysis and Mayer bond order. Such character is completely different from that for early transition metal–SO complexes and dioxygen complexes of platinum. Formation of the PtF(2)(η(1)-SO) complex was found to occur via the consecutive transfer of the two fluorine atoms from SOF(2) to Pt in the sulfur bound Pt(SOF(2)) complex, which involves a series of intermediates on the basis of the mechanism study at the B3LYP level. Although the whole process is hindered by the large energy barrier encountered during the transfer of the first fluorine atom, UV-vis irradiation can provide sufficient energy to surmount this barrier and facilitates the formation of the nonplanar PtF(2)(η(1)-SO) complex stabilized in matrix.