Inokuchi, YoshiyaKaneko, MasashiHonda, TakumiNakashima, SatoruEbata, TakayukiRizzo, Thomas R.2017-02-232017-02-232017-02-23201710.1021/acs.inorgchem.6b02134https://infoscience.epfl.ch/handle/20.500.14299/134720WOS:000391248900032We measure UV and IR spectra in the gas phase for EuOH+, EuCl+, and TbO+ ions, which are produced by an electrospray ionization source and cooled to similar to 10 K in a cold, 22-pole ion trap. The UV photodissociation (UVPD) spectra of these ions show a number of sharp, well-resolved bands in the 30000-38000 cm(-1) region, although a definite assignment of the spectra is difficult because of a high degree of congestion. We also measure an IR spectrum of the EuOH+ ion in the 3500-3800 cm(-1) region by IR-UV double-resonance spectroscopy, which reveals an OH stretching band at 3732 cm(-1). We perform density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations of these ions in order to examine the nature of the transitions. The DFT results indicate that the states of highest-spin multiplicity (octet for EuOH+ and EuCl+ and septet for TbO+) are substantially more stable than other states of lower-spin multiplicity. The TD-DFT calculations suggest that UV absorption of the EuOH+ and EuCl+ ions arises from Eu(4f) -> Eu(5d,6p) transitions, whereas electronic transitions of the TbO+ ion are mainly due to the electron promotion of O(2p) -> Tb(4f,6s). The UVPD results of the lanthanide-containing ions in this study suggest the possibility of using lanthanide ions as "conformation reporters" for gas-phase spectroscopy for large molecules.text::journal::journal article::research article