Facebook Twitter Instagram YouTube

Infrared Photodissociation Spectra of [Sn(CO2)n]- Cluster Ions

TitleInfrared Photodissociation Spectra of [Sn(CO2)n]- Cluster Ions
Publication TypeJournal Article
Year of Publication2018
AuthorsThompson, MC, J. Weber, M
JournalThe Journal of Physical Chemistry A
Pagination3772 - 3779
Date Published2018-03

We present infrared spectra and density functional theory calculations of mass selected [Sn(CO2)n] cluster anions (n = 2–6). The spectra and structures of these clusters exhibit less structural diversity than those of analogous clusters with first-row transition metals, but are more complex than those for the heavy coinage metals or for the related [Bi(CO2)n] clusters. The most favorable core ion structure for all cluster sizes can be characterized as a Sn-oxalate complex, Sn[C2O4]. Higher energy isomers based on a bidentate η2-(C,O) CO2 ligand tightly bound to the metal atom in SnCO2 complexes are also observed, even for the largest cluster sizes studied here. For n = 2, another high energy isomer is found, featuring a CO2 ligand weakly bound to the metal atom in a SnCO2 ion.


JILA follows the six University nodes' policies for ensuring harassment-free environments. For more detailed information regarding the University of Colorado policies, please read the Discrimination and Harassment Policy and Procedures.