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dc.contributor.authorWang, Yi-Yingen_US
dc.contributor.authorChung, Chao-Yuen_US
dc.contributor.authorLee, Yuan-Pernen_US
dc.date.accessioned2017-04-21T06:55:53Z-
dc.date.available2017-04-21T06:55:53Z-
dc.date.issued2016-10-21en_US
dc.identifier.issn0021-9606en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.4964658en_US
dc.identifier.urihttp://hdl.handle.net/11536/132880-
dc.description.abstractCriegee intermediates are carbonyl oxides that play critical roles in the ozonolysis of alkenes in the atmosphere. So far, the infrared spectra of only the simplest Criegee intermediates CH2OO and CH3CHOO are reported. We report the transient infrared spectrum of the next member (CH3)(2)COO, produced from ultraviolet irradiation of a mixture of (CH3)(2)CI2 + O-2 in a flow reactor and detected with a step-scan Fourier-transform spectrometer. The four observed bands near 1424, 1368, 1040, and 887.4 cm(-1) provide definitive identification of (CH3)(2)COO. The observed vibrational wavenumbers and rotational contours agree with those predicted with quantum-chemical calculations; contributions of the hot bands from excited states of the low-lying torsional modes are significant. The rapid decay yields an estimate of the rate coefficient similar to 1.6 x 10(-10) cm(3) molecule(-1) s(-1) for the self-reaction of (CH3)(2)COO. The direct IR detection of (CH3)(2)COO should prove useful for field measurements and laboratory investigations of related Criegee mechanism. Published by AIP Publishing.en_US
dc.language.isoen_USen_US
dc.titleInfrared spectral identification of the Criegee intermediate (CH3)(2)COOen_US
dc.identifier.doi10.1063/1.4964658en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.citation.volume145en_US
dc.citation.issue15en_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:000386916500023en_US
Appears in Collections:Articles