Torsional features in the (3s)S-1 <- S-0 transition of N-methylpyrrole and C4D4NCH3

dc.contributor.authorPhilis, J. G.en
dc.date.accessioned2015-11-24T18:26:43Z
dc.date.available2015-11-24T18:26:43Z
dc.identifier.issn0022-2860-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/15939
dc.rightsDefault Licence-
dc.subjectn-methylpyrroleen
dc.subjectmethyl torsional transitionsen
dc.subjectrempien
dc.subjectelectronic excitationen
dc.subjectpyrroleen
dc.subjectfuranen
dc.subjectstatesen
dc.subjectcyclopentadieneen
dc.subjectspectraen
dc.subjectabsorptionen
dc.subjectmoleculesen
dc.subjectbanden
dc.subjects-0en
dc.titleTorsional features in the (3s)S-1 <- S-0 transition of N-methylpyrrole and C4D4NCH3en
heal.abstractThe one-photon and two-photon S-1 <-- S-0 REMPI spectra of jet-cooled N-methylpyrrole-ring-d(4) (C4D4NCH3, NMPd4) were studied and compared to the corresponding spectra of N-methylpyrrole (C4H4NCH3, NMP). This electronic transition is the electric dipole forbidden 3sA(2) <-- A(1) Rydberg excitation. The transition is allowed in two-photon spectroscopy and the origin was found in the two-photon spectra at 41,193 and 42,015 cm(-1) for NMP and NMPd4, respectively. Exactly the same low-frequency pattern is present close to the absent origin in the one-photon spectra of NMP and NMPd4. The assignment of these features to methyl internal rotational transitions is confirmed. (C) 2003 Elsevier Science B.V. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondary<Go to ISI>://000183424200075-
heal.journalNameJournal of Molecular Structureen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2003-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών και Τεχνολογιών. Τμήμα Βιολογικών Εφαρμογών και Τεχνολογιώνel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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