Electronic spectra of carbon chain anions: C2nH- (n=5-12)

D. A. Kirkwood*, M. Tulej, M. V. Pachkov, M. Schnaiter, F. Güthe, M. Grutter, M. Wyss, J. P. Maier, G. Fischer

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    20 Citations (Scopus)

    Abstract

    The electronic absorption spectra of mono-hydrogenated carbon chain anions C2nH- (n=5-10) have been measured in the gas-phase and in 6 K neon matrices (n=8-12). The techniques of resonant two-color electron photodetachment in the gas-phase and absorption spectroscopy of mass-selected anions in neon matrix were used. A homologous series is observed, with band system origins shifting from 304 nm for C10H- to 590 nm for C20H-. In conjunction with ab initio calculations the band systems are attributed 1+ ← + X 1+ transition of linear acetylenic anions. Another near lying electronic transition due to a second isomer is also apparent for C10H- up to C24H-. Comparison with tables of the known diffuse interstellar bands indicates possible matches for the origin bands of the C18H- and C20H- isomers.

    Original languageEnglish
    Pages (from-to)9280-9286
    Number of pages7
    JournalJournal of Chemical Physics
    Volume111
    Issue number20
    DOIs
    Publication statusPublished - 22 Nov 1999

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