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    Wei Li, Jia-ye Jin, Hui Qu, Guan-jun Wang, Ming-fei Zhou. Infrared Photodissociation Spectroscopic and Theoretical Study of the HC2nO+ (n=3-6) Cations[J]. Chinese Journal of Chemical Physics , 2019, 32(1): 77-83. DOI: 10.1063/1674-0068/cjcp1811254
    Citation: Wei Li, Jia-ye Jin, Hui Qu, Guan-jun Wang, Ming-fei Zhou. Infrared Photodissociation Spectroscopic and Theoretical Study of the HC2nO+ (n=3-6) Cations[J]. Chinese Journal of Chemical Physics , 2019, 32(1): 77-83. DOI: 10.1063/1674-0068/cjcp1811254

    Infrared Photodissociation Spectroscopic and Theoretical Study of the HC2nO+ (n=3-6) Cations

    • The carbon chain cations, HC2nO+ (n=3-6) are produced via a pulsed laser vaporization supersonic expansion ion source in the gas phase. Their infrared spectra are measured via mass-selected infrared photodissociation spectroscopy of the CO “tagged” HC2nO·CO+ cation complexes in 1600-3500 cm-1 frequency range. The geometric and electronic structures of the HC2nO·CO+ complexes and the core HC2nO+ (n=3-6) cations are determined with the aid of density functional theory calculations. These HC2nO+(n=3-6) ions are identified to be linear carbon chain derivatives terminally capped by hydrogen and oxygen. The triplet ground states are 10-15 kcal/mol lower in energy than the singlet states, indicating cumulene-like carbon chain structures.
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