Tracking the Metal-Centered Triplet in Photoinduced Spin Crossover of Fe(phen) with Tabletop Femtosecond M-Edge X-ray Absorption Near-Edge Structure Spectroscopy.

Fe(II) coordination complexes are promising alternatives to Ru(II) and Ir(III) chromophores for photoredox chemistry and solar energy conversion, but rapid deactivation of the initial metal-to-ligand charge transfer (MLCT) state to low-lying (d,d) states limits their performance. Relaxation to a long-lived quintet state is postulated to occur via a metal-centered triplet state, but this mechanism remains controversial. We use femtosecond extreme ultraviolet (XUV) transient absorption spectroscopy to measure the excited-state relaxation of Fe(phen) and conclusively identify a T intermediate that forms in 170 fs and decays to a vibrationally hot T state in 39 fs. A coherent vibrational wavepacket with a period of 249 fs and damping time of 0.63 ps is observed on the T surface, and the spectrum of this oscillation serves as a fingerprint for the Fe-N symmetric stretch. The results show that the shape of the M-edge X-ray absorption near-edge structure (XANES) spectrum is sensitive to the electronic structure of the metal center, and the high-spin sensitivity, fast time resolution, and tabletop convenience of XUV transient absorption make it a powerful tool for studying the complex photophysics of transition metal complexes.