We measured the electronic spectra of mass-selected [M(bpy)3]2+ (M = Fe and Os, bpy = 2,2′-bipyridine) ions in vacuo by photodissociation spectroscopy of their N2 adducts, [M(bpy)3]2+·N2. Extensive band systems in the visible (predominantly charge transfer) and near-ultraviolet (ππ*) spectral regions are reported. The [M(bpy)3]2+·N2 target ions were prepared by condensing N2 onto electrosprayed ions in a cryogenic ion trap at ca. 25 K and then mass-selected by time-of-flight mass spectrometry. The electronic photodissociation spectra of the cold, gas-phase ions closely reflect their intrinsic properties, i.e., without perturbation by solvent effects. The spectra are interpreted using time-dependent density functional theory calculations both with and without accounting for relativistic effects.
DOI: 10.1021/acs.inorgchem.7b00620
Shuang Xu†, James E. T. Smith‡, and J. Mathias Weber‡
† JILA and Department of Physics, University of Colorado, Boulder, Colorado 80309-0440, United States
‡ JILA and Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309-0440, United States