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dc.contributor.authorChiang, SYen_US
dc.contributor.authorFang, YSen_US
dc.contributor.authorSankaran, Ken_US
dc.contributor.authorLee, YPen_US
dc.date.accessioned2014-12-08T15:39:36Z-
dc.date.available2014-12-08T15:39:36Z-
dc.date.issued2004-02-15en_US
dc.identifier.issn0021-9606en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.1641010en_US
dc.identifier.urihttp://hdl.handle.net/11536/27035-
dc.description.abstractThe dissociative photoionization of CH2Br2 in a region similar to10-24 eV was investigated with photoionization mass spectroscopy using a synchrotron radiation source. An adiabatic ionization energy of 10.25 eV determined for CH2Br2 agrees satisfactorily with predictions of 10.26 and 10.25 eV with G2 and G3 methods, respectively. Observed major fragment ions CH2Br+, CHBr+, and CBr+ show appearance energies at 11.22, 12.59, and 15.42 eV, respectively; minor fragment ions CHBr2+, Br+, and CH2+ appear at 12.64, 15.31, and 16.80 eV, respectively. Energies for formation of observed fragment ions and their neutral counterparts upon ionization of CH2Br2 are computed with G2 and G3 methods. Dissociative photoionization channels associated with six observed fragment ions are proposed based on comparison of determined appearance energies and predicted energies. An upper limit of DeltaH(f,298)(0)(CHBr+)less than or equal to300.7+/-1.5 kcal mol(-1) is derived experimentally; the adiabatic ionization energy of CHBr is thus derived to be less than or equal to9.17+/-0.23 eV. Literature values for DeltaH(f,298)(0)(CBr+)=362.5 kcal mol(-1) and ionization energy of 10.43 eV for CBr are revised to be less than 332 kcal mol(-1) and 9.11 eV, respectively. Also based on a new experimental ionization energy, DeltaH(f,298)(0)(CH2Br2+) is revised to be 236.4+/-1.5 kcal mol(-1). (C) 2004 American Institute of Physics.en_US
dc.language.isoen_USen_US
dc.titleExperimental and quantum-chemical studies on photoionization and dissociative photoionization of CH2Br2en_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.1641010en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.citation.volume120en_US
dc.citation.issue7en_US
dc.citation.spage3270en_US
dc.citation.epage3276en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000188880900027-
dc.citation.woscount13-
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