Matrix Isolation Spectroscopic and Relativistic Quantum Chemical Study of Molecular Platinum Fluorides PtFn (n=1-6) Reveals Magnetic Bistability of PtF4.

Molecular platinum fluorides PtFn , n=1-6, are prepared by two different routes, photo-initiated fluorine elimination from PtF6 embedded in solid noble-gas matrices, and the reaction of elemental fluorine with laser-ablated platinum atoms. IR spectra of the reaction products isolated in rare-gas matrices under cryogenic conditions provide, for the first time, experimental vibrational frequencies of molecular PtF3 , PtF4 and PtF5 . Photolysis of PtF6 enabled a highly efficient and almost quantitative formation of molecular PtF4 , whereas both PtF5 and PtF3 were formed simultaneously by subsequent UV irradiation of PtF4 . The vibrational spectra of these molecular platinum fluorides were assigned with the help of one- and two-component quasirelativistic DFT computation to account for scalar relativistic and spin-orbit coupling effects. Competing Jahn-Teller and spin-orbit coupling effects result in a magnetic bistability of PtF4 , for which a spin-triplet (3 B2g , D2h ) coexists with an electronic singlet state (1 A1g , D4h ) in solid neon matrices.