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Article: Picosecond time-resolved resonance Raman observation of the iso-CH2Cl-I and iso-CH2I-Cl photoproducts from the "photoisomerization" reactions of CH 2ICl in the solution phase

TitlePicosecond time-resolved resonance Raman observation of the iso-CH2Cl-I and iso-CH2I-Cl photoproducts from the "photoisomerization" reactions of CH 2ICl in the solution phase
Authors
Kwok, WMMa, CParker, AWPhillips, DTowrie, MMatousek, PZheng, XPhillips, DL
KeywordsPhysics chemistry
Issue Date2001
PublisherAmerican Institute of Physics. The Journal's web site is located at http://jcp.aip.org/jcp/staff.jsp
Citation
Journal of Chemical Physics, 2001, v. 114 n. 17, p. 7536-7543 How to Cite?
DOI: http://dx.doi.org/10.1063/1.1362178
AbstractA preliminary pecosecond Stokes time-resolved resonance Raman investigation was made of the initial formation and subsequent decay of the photoproduct produced following 267 nm excitaiton of CH 2ClI in acetonitrile solution. A coparision was made between density-functional theroy computations for portable photoproduct species and the results from a femtosecond transient absorption study to Raman spectra. This comparision indicated that the iso-CH 2ClI was aminly produced and associated with the 460 nm transient absorption band.
Persistent Identifierhttp://hdl.handle.net/10722/42355
ISSN
0021-9606
2023 Impact Factor: 3.1
2023 SCImago Journal Rankings: 1.101
ISI Accession Number ID
WOS:000168168100027
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorKwok, WMen_HK
dc.contributor.authorMa, Cen_HK
dc.contributor.authorParker, AWen_HK
dc.contributor.authorPhillips, Den_HK
dc.contributor.authorTowrie, Men_HK
dc.contributor.authorMatousek, Pen_HK
dc.contributor.authorZheng, Xen_HK
dc.contributor.authorPhillips, DLen_HK
dc.date.accessioned2007-01-29T08:47:38Z-
dc.date.available2007-01-29T08:47:38Z-
dc.date.issued2001en_HK
dc.identifier.citationJournal of Chemical Physics, 2001, v. 114 n. 17, p. 7536-7543-
dc.identifier.issn0021-9606en_HK
dc.identifier.urihttp://hdl.handle.net/10722/42355-
dc.description.abstractA preliminary pecosecond Stokes time-resolved resonance Raman investigation was made of the initial formation and subsequent decay of the photoproduct produced following 267 nm excitaiton of CH 2ClI in acetonitrile solution. A coparision was made between density-functional theroy computations for portable photoproduct species and the results from a femtosecond transient absorption study to Raman spectra. This comparision indicated that the iso-CH 2ClI was aminly produced and associated with the 460 nm transient absorption band.en_HK
dc.format.extent110091 bytes-
dc.format.extent30208 bytes-
dc.format.mimetypeapplication/pdf-
dc.format.mimetypeapplication/msword-
dc.languageengen_HK
dc.publisherAmerican Institute of Physics. The Journal's web site is located at http://jcp.aip.org/jcp/staff.jspen_HK
dc.relation.ispartofJournal of Chemical Physicsen_HK
dc.rightsCopyright 2001 American Institute of Physics. This article may be downloaded for personal use only. Any other use requires prior permission of the author and the American Institute of Physics. The following article appeared in Journal of Chemical Physics, 2001, v. 114 n. 17, p. 7536-7543 and may be found at https://doi.org/10.1063/1.1362178-
dc.subjectPhysics chemistryen_HK
dc.titlePicosecond time-resolved resonance Raman observation of the iso-CH2Cl-I and iso-CH2I-Cl photoproducts from the "photoisomerization" reactions of CH 2ICl in the solution phaseen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0021-9606&volume=114&issue=17&spage=7536&epage=7543&date=2001&atitle=Picosecond+time-resolved+resonance+Raman+observation+of+the+iso-CH2Cl-l+and+iso-CH2I-Cl+photoproducts+from+the+%27photoisomerization%27+reactions+of+CH2ICl+in+the+solution+phaseen_HK
dc.identifier.emailMa, C:macs@hkucc.hku.hken_HK
dc.identifier.emailPhillips, DL:phillips@hku.hken_HK
dc.identifier.authorityMa, C=rp00758en_HK
dc.identifier.authorityPhillips, DL=rp00770en_HK
dc.embargo.remarkduplicate of handle # 42351-
dc.description.naturepublished_or_final_versionen_HK
dc.identifier.doi10.1063/1.1362178en_HK
dc.identifier.scopuseid_2-s2.0-0035335285en_HK
dc.identifier.hkuros73844-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0035335285&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume114en_HK
dc.identifier.issue17en_HK
dc.identifier.spage7536en_HK
dc.identifier.epage7543en_HK
dc.identifier.isiWOS:000168168100027-
dc.publisher.placeUnited Statesen_HK
dc.identifier.scopusauthoridKwok, WM=7103129332en_HK
dc.identifier.scopusauthoridMa, C=7402924979en_HK
dc.identifier.scopusauthoridParker, AW=7403267977en_HK
dc.identifier.scopusauthoridPhillips, D=22998496000en_HK
dc.identifier.scopusauthoridTowrie, M=7004415080en_HK
dc.identifier.scopusauthoridMatousek, P=7005659005en_HK
dc.identifier.scopusauthoridZheng, X=7404090253en_HK
dc.identifier.scopusauthoridPhillips, DL=7404519365en_HK
dc.identifier.issnl0021-9606-

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