Origin of core-to-core x-ray emission spectroscopy sensitivity to structural dynamics.

Recently, coherent structural dynamics in the excited state of an iron photosensitizer was observed through oscillations in the intensity of K x-ray emission spectroscopy (XES). Understanding the origin of the unexpected sensitivity of core-to-core transitions to structural dynamics is important for further development of femtosecond time-resolved XES methods and, we believe, generally necessary for interpretation of XES signals from highly non-equilibrium structures that are ubiquitous in photophysics and photochemistry. Here, we use multiconfigurational wavefunction calculations combined with atomic theory to analyze the emission process in detail. The sensitivity of core-to-core transitions to structural dynamics is due to a shift of the minimum energy metal-ligand bond distance between 1 and 2 core-hole states. A key effect is the additional contraction of the non-bonding 3 and 3 orbitals in 1 core-hole states, which decreases electron-electron repulsion and increases overlap in the metal-ligand bonds. The effect is believed to be general and especially pronounced for systems with strong bonds. The important role of 3 and 3 orbitals is consistent with the analysis of radial charge and spin densities and can be connected to the negative chemical shift observed for many transition metal complexes. The XES sensitivity to structural dynamics can be optimized by tuning the emission energy spectrometer, with oscillations up to ±4% of the maximum intensity for the current system. The theoretical predictions can be used to design experiments that separate electronic and nuclear degrees of freedom in ultrafast excited state dynamics.