Abstract

The excited state dynamics of a d0 vanadium(V) oxido ligand-to-metal charge transfer (LMCT) complex, VOLF, were investigated via a combination of static optical and X-ray absorption (XAS) spectroscopy, transient optical absorption spectroscopy, and time-dependent density functional theory (TD-DFT). Upon excitation of the LMCT in the visible region, transient absorption data reveal that internal conversion traps the excited carrier population into a long-lived charge transfer state of 3dxy electron character, S1(dxy). The internal conversion is substantiated by an isosbestic point in the transient absorption data, two nearby charge transfer states that couple well by TD-DFT, multiple rates in the ground state recovery, and the decay kinetics of an excited state absorption with the energy of a d-d transition in O K-edge XAS spectra. The long lifetime (∼420 ps) of S1(dxy) can be ascribed to its poor optical and vibrational coupling to a distorted ground state (S0*) via a negligible electronic dipole transiti...

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