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Communication: Electronic transition of the l-C6 + cation at 417 nm.
Colley, Jason E; Orr, Dylan S; Duncan, Michael A.
Afiliación
  • Colley JE; Department of Chemistry, University of Georgia, Athens, Georgia 30602, USA.
  • Orr DS; Department of Chemistry, University of Georgia, Athens, Georgia 30602, USA.
  • Duncan MA; Department of Chemistry, University of Georgia, Athens, Georgia 30602, USA.
J Chem Phys ; 157(12): 121102, 2022 Sep 28.
Article en En | MEDLINE | ID: mdl-36182433
ABSTRACT
A new electronic transition is reported for the linear C6 + cation with an origin at 416.8 nm. This spectrum can be compared to the matrix isolation spectra at lower energies reported previously by Fulara et al. [J. Chem. Phys. 123, 044305 (2005)], which assigned linear and cyclic isomers, and to the gas phase spectrum reported previously by Campbell and Dunk [Rev. Sci. Instrum. 90, 103101 (2019)], which detected the same cyclic-isomer spectrum reported by Fulara. Comparisons to electronically excited states and vibrations predicted by various forms of theory allow assignment of the spectrum to a new electronic state of linear C6 +. The spectrum consists of a strong origin band, two vibronic progression members at higher energy and four hot bands at lower energies. The hot bands provide the first gas phase information on ground state vibrational frequencies. The vibrational and electronic structure of C6 + provide a severe challenge to computational chemistry.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Chem Phys Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Chem Phys Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos