Unraveling Metal-Ligand Bonding in an HNO-Evolving {FeNO} 6 Complex with a Combined X-ray Spectroscopic Approach.

Photolytic delivery of nitric oxide and nitroxide has substantial biomedical and phototherapeutic applications. Here, we utilized hard X-ray spectroscopic methods to identify key geometric and electronic structural features of two photolabile {FeNO} 6 complexes where the compounds differ in the presence of a pendant thiol in [Fe(NO)( TMS PS2)( TMS PS2H)] and thioether in [Fe(NO)( TMS PS2)( TMS PS2CH 3 )] with the former complex being the only transition metal system to photolytically generate HNO. Fe Kβ XES identifies the photoreactant systems as essentially Fe(II)-NO + , while valence-to-core XES extracts a NO oxidation state of +0.5. Finally, the pre-edge of the Fe high-energy-resolution fluorescence detected (HERFD) XAS spectra is shown to be acutely sensitive to perturbation of the Fe-NO covalency enhanced by the 3d-4p orbital mixing dipole intensity contribution. Collectively, this X-ray spectroscopic approach enables future time-resolved insights in these systems and extensions to other challenging redox noninnocent {FeNO} x systems.