Back to Search Start Over

Characterization of the vibrational properties of copper difluoride anion and neutral ground states via direct and indirect photodetachment spectroscopy.

Authors :
Lyle, Justin
Chandramoulee, Sudharson Ravishankar
Hamilton, Jacob R.
Traylor, Blaine A.
Guasco, Timothy L.
Jagau, Thomas-C.
Mabbs, Richard
Source :
Journal of Chemical Physics; 8/28/2018, Vol. 149 Issue 8, pN.PAG-N.PAG, 8p, 3 Charts, 3 Graphs
Publication Year :
2018

Abstract

Photoelectron spectra of <superscript>63</superscript>CuF<subscript>2</subscript><superscript>−</superscript> are reported at wavelengths 310 nm, 346.6 nm, and 350.1 nm, obtained via velocity map imaging. The photoelectron angular distributions allow for the unambiguous assignment of a <superscript>2</superscript>Σ<subscript>g</subscript><superscript>+</superscript> neutral CuF<subscript>2</subscript> ground state. Vibrational analysis of the direct detachment transitions in the spectra enables accurate determination of the anion and neutral bond length difference (0.073 Å), adiabatic electron affinity of CuF<subscript>2</subscript> (3.494 eV) and symmetric stretching (500 cm<superscript>−1</superscript>, anion, and 630 cm<superscript>−1</superscript>, neutral) and antisymmetric stretching (610 cm<superscript>−1</superscript>, anion, and 782 cm<superscript>−1</superscript> neutral) frequencies of the ground electronic states. Strongly photon energy dependent intensities are also observed for select transitions. Equation-of-motion coupled-cluster singles and doubles calculations augmented by a complex absorbing potential reveal a metastable <superscript>1</superscript>Π<subscript>g</subscript> anion state which is optically accessible due to Renner-Teller coupling. Mediation of the detachment process by this state allows measurement of the bending frequencies (177 cm<superscript>−1</superscript>, anion, and 200 cm<superscript>−1</superscript>, neutral) completing the inventory of experimentally measured vibrational properties of the ground electronic states. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219606
Volume :
149
Issue :
8
Database :
Complementary Index
Journal :
Journal of Chemical Physics
Publication Type :
Academic Journal
Accession number :
131635721
Full Text :
https://doi.org/10.1063/1.5040122