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dc.contributor.authorBahou, Mohammeden_US
dc.contributor.authorChou, Sheng-Lungen_US
dc.contributor.authorWu, Yu-Jongen_US
dc.date.accessioned2020-07-01T05:22:09Z-
dc.date.available2020-07-01T05:22:09Z-
dc.date.issued2020-06-05en_US
dc.identifier.issn0022-2860en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.molstruc.2020.127995en_US
dc.identifier.urihttp://hdl.handle.net/11536/154564-
dc.description.abstractWe recorded the IR spectra of 2-C16R11 and 4-C16R11 trapped in solid para-hydrogen (p-H-2). These species were produced on the electron bombardment of p-H-2 containing pyrene (C16H10) in a small proportion during matrix deposition. IR absorption features of 1-C16H11+ and 1-C16H11 in solid p-H-2 were previously identified [J. Phys. Chem. Lett. 4 (2013) 1989]. Here, the irradiation of a similar matrix sample at 365 nm depleted 1-C(16)H(11)(+ )and 2-C16H11 and produced 1-C16H11 and 4-C16H11. In contrast, irradiation at 405 nm decreased 1-C16H11+, 2-C16H11 and 4-C16H11. The identification of the observed lines of 2-C16H11, and 4-C16H11 was supported by predictions of the vibrational wavenumbers and relative IR intensities at the B3PW91/6-311++G(2d,2p) level of theory. (C) 2020 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleFormation and infrared spectra of monohydrogenated pyrenes 2-C16H11 and 4-C16H11 trapped in solid para-hydrogenen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.molstruc.2020.127995en_US
dc.identifier.journalJOURNAL OF MOLECULAR STRUCTUREen_US
dc.citation.volume1209en_US
dc.citation.spage0en_US
dc.citation.epage0en_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:000522727600019en_US
dc.citation.woscount1en_US
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