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dc.contributor.authorWu, Yu-Jongen_US
dc.contributor.authorLin, Meng-Yehen_US
dc.contributor.authorCheng, Bing-Mingen_US
dc.contributor.authorChen, Hui-Fenen_US
dc.contributor.authorLee, Yuan-Pernen_US
dc.date.accessioned2014-12-08T15:12:09Z-
dc.date.available2014-12-08T15:12:09Z-
dc.date.issued2008-05-28en_US
dc.identifier.issn0021-9606en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.2929826en_US
dc.identifier.urihttp://hdl.handle.net/11536/9319-
dc.description.abstractIrradiation of samples of solid Ne near 3.0 K containing ethene (C(2)H(4)) with vacuum ultraviolet radiation at 120 nm from synchrotron yielded new spectral lines at 3141.0, 2953.6, 2911.5, 1357.4, 677.1, 895.3, and 857.0 cm(-1). These features are assigned to alpha-CH stretching (nu(1)), CH(2) antisymmetric stretching (nu(2)), CH(2) symmetric stretching (nu(3)), CH(2)-bending (nu(5)), HCCH cis bending (nu(7)), CH(2) out-of-plane bending (nu(8)), and alpha-CH out-of-plane bending (nu(9)) modes of C(2)H(3), respectively, based on results of (13)C- and D-isotopic experiments and quantum-chemical calculations. These calculations using density-functional theory (B3LYP and PW91PW91/aug-cc-pVTZ) predict vibrational wavenumbers, IR intensities, and isotopic ratios of vinyl radical that agree satisfactorily with our experimental results. (C) 2008 American Institute of Physics.en_US
dc.language.isoen_USen_US
dc.titleInfrared absorption spectra of vinyl radicals isolated in solid Neen_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.2929826en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.citation.volume128en_US
dc.citation.issue20en_US
dc.citation.epageen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000256304200035-
dc.citation.woscount18-
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