Ultrafast Photochemistry of the [Cr(NCS)] Complex in Dimethyl Sulfoxide and Dimethylformamide upon Excitation into Ligand-Field Electronic State.

The ultrafast photochemistry of the [Cr(NCS)] complex upon excitation to the T ligand-field (LF) state was studied in dimethyl sulfoxide (DMSO) and ,-dimethylformamide (DMF) in a wide temporal range (100 fs to 9 ms) by a combination of femtosecond and nanosecond transient absorption spectroscopy techniques and supported by quantum-chemical DFT/TD-DFT calculations. The initially excited T state undergoes intersystem crossing to the vibrationally hot E state with time constants of 1.1 ± 0.2 and 1.8 ± 0.1 ps in DMSO and DMF, respectively. Vibrational relaxation occurs in the same time scale and takes 1-5 ps. A major part of the [Cr(NCS)] complex in the E state undergoes intersystem crossing to the ground state with time constants of 65 ± 5 and 85 ± 5 ns in DMSO and DMF, respectively. A minor part of electronically excited [Cr(NCS)] undergoes irreversible photochemical decomposition. In DMSO, the photolysis of the [Cr(NCS)] complex results in single or double isothiocyanate ion release followed by the coordination of the solvent molecules with a time constant of 1 ± 0.2 ms.