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Article: Nanosecond time-resolved resonance Raman investigation of the radical cation of 4,4′-dibromobiphenyl and the T1→Tn transition of 4,4′-dibromobiphenyl

TitleNanosecond time-resolved resonance Raman investigation of the radical cation of 4,4′-dibromobiphenyl and the T1→Tn transition of 4,4′-dibromobiphenyl
Authors
Pan, DShoute, LCTPhillips, DL
Issue Date1998
PublisherElsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/cplett
Citation
Chemical Physics Letters, 1998, v. 292 n. 4-6, p. 677-685 How to Cite?
DOI: http://dx.doi.org/10.1016/S0009-2614(98)00735-0
AbstractWe have taken nanosecond time-resolved resonance Raman spectra of the T1 → Tn transition of 4,4′-dibromobiphenyl in cyclohexane solution and of the radical cation of 4,4′-dibromobiphenyl in acetonitrile solution. The resonance Raman spectrum of T1 4,4′-dibromobiphenyl is consistent with a planar quinoidal structure. The C-Br bond appears stronger in the T1 state than in the S0 ground state and this is in agreement with photochemistry studies done for 4-bromobiphenyl that indicate that the T1 state must be further excited by excimer formation and/or electron transfer with an appropriate donor prior to a debromination reaction.
Persistent Identifierhttp://hdl.handle.net/10722/167295
ISSN
0009-2614
2023 Impact Factor: 2.8
2023 SCImago Journal Rankings: 0.502
ISI Accession Number ID
WOS:000075482300048
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorPan, Den_US
dc.contributor.authorShoute, LCTen_US
dc.contributor.authorPhillips, DLen_US
dc.date.accessioned2012-10-08T03:05:22Z-
dc.date.available2012-10-08T03:05:22Z-
dc.date.issued1998en_US
dc.identifier.citationChemical Physics Letters, 1998, v. 292 n. 4-6, p. 677-685en_US
dc.identifier.issn0009-2614en_US
dc.identifier.urihttp://hdl.handle.net/10722/167295-
dc.description.abstractWe have taken nanosecond time-resolved resonance Raman spectra of the T1 → Tn transition of 4,4′-dibromobiphenyl in cyclohexane solution and of the radical cation of 4,4′-dibromobiphenyl in acetonitrile solution. The resonance Raman spectrum of T1 4,4′-dibromobiphenyl is consistent with a planar quinoidal structure. The C-Br bond appears stronger in the T1 state than in the S0 ground state and this is in agreement with photochemistry studies done for 4-bromobiphenyl that indicate that the T1 state must be further excited by excimer formation and/or electron transfer with an appropriate donor prior to a debromination reaction.en_US
dc.languageengen_US
dc.publisherElsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/cpletten_US
dc.relation.ispartofChemical Physics Lettersen_US
dc.titleNanosecond time-resolved resonance Raman investigation of the radical cation of 4,4′-dibromobiphenyl and the T1→Tn transition of 4,4′-dibromobiphenylen_US
dc.typeArticleen_US
dc.identifier.emailPhillips, DL:phillips@hku.hken_US
dc.identifier.authorityPhillips, DL=rp00770en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1016/S0009-2614(98)00735-0-
dc.identifier.scopuseid_2-s2.0-0000721068en_US
dc.identifier.hkuros40234-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0000721068&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume292en_US
dc.identifier.issue4-6en_US
dc.identifier.spage677en_US
dc.identifier.epage685en_US
dc.identifier.isiWOS:000075482300048-
dc.publisher.placeNetherlandsen_US
dc.identifier.scopusauthoridPan, D=7202085030en_US
dc.identifier.scopusauthoridShoute, LCT=6701331171en_US
dc.identifier.scopusauthoridPhillips, DL=7404519365en_US
dc.identifier.issnl0009-2614-

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