Coriolis effects on “intermediate case” of intramolecular vibrational relaxation: Rotational-temperature dependence of energy- resolved fluorescence from jet-cooled perylene with 776–975 cm−1 excess energies
Identifieur interne : 004235 ( Main/Merge ); précédent : 004234; suivant : 004236Coriolis effects on “intermediate case” of intramolecular vibrational relaxation: Rotational-temperature dependence of energy- resolved fluorescence from jet-cooled perylene with 776–975 cm−1 excess energies
Auteurs : B. E. Forch [États-Unis] ; K. T. Chen [États-Unis] ; E. C. Lim [États-Unis]Source :
- Chemical Physics Letters [ 0009-2614 ] ; 1983.
Abstract
The rotational-temperature dependence of the energy-resolved fluorescence, combined with the calculated level density, indicates that the large variations in the rate of the intramolecular vibrational relaxation over a small excess energy in S1 perylene is due to the fluctuations in the density of accessible vibrational levels, resulting from the vibrational selection rules for second-order Coriolis coupling.
Url:
DOI: 10.1016/0009-2614(83)87335-7
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 003C31
- to stream Istex, to step Curation: 003963
- to stream Istex, to step Checkpoint: 003188
Links to Exploration step
ISTEX:75471EDB10C1B0717A6956F64259C9AC1D153C02Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Coriolis effects on “intermediate case” of intramolecular vibrational relaxation: Rotational-temperature dependence of energy- resolved fluorescence from jet-cooled perylene with 776–975 cm−1 excess energies</title>
<author><name sortKey="Forch, B E" sort="Forch, B E" uniqKey="Forch B" first="B. E." last="Forch">B. E. Forch</name>
</author>
<author><name sortKey="Chen, K T" sort="Chen, K T" uniqKey="Chen K" first="K. T." last="Chen">K. T. Chen</name>
</author>
<author><name sortKey="Lim, E C" sort="Lim, E C" uniqKey="Lim E" first="E. C." last="Lim">E. C. Lim</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:75471EDB10C1B0717A6956F64259C9AC1D153C02</idno>
<date when="1983" year="1983">1983</date>
<idno type="doi">10.1016/0009-2614(83)87335-7</idno>
<idno type="url">https://api.istex.fr/document/75471EDB10C1B0717A6956F64259C9AC1D153C02/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">003C31</idno>
<idno type="wicri:Area/Istex/Curation">003963</idno>
<idno type="wicri:Area/Istex/Checkpoint">003188</idno>
<idno type="wicri:doubleKey">0009-2614:1983:Forch B:coriolis:effects:on</idno>
<idno type="wicri:Area/Main/Merge">004235</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Coriolis effects on “intermediate case” of intramolecular vibrational relaxation: Rotational-temperature dependence of energy- resolved fluorescence from jet-cooled perylene with 776–975 cm−1 excess energies</title>
<author><name sortKey="Forch, B E" sort="Forch, B E" uniqKey="Forch B" first="B. E." last="Forch">B. E. Forch</name>
<affiliation wicri:level="1"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Chemistry, Wayne State University, Detroit, Michigan 48202</wicri:regionArea>
<wicri:noRegion>Michigan 48202</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Chen, K T" sort="Chen, K T" uniqKey="Chen K" first="K. T." last="Chen">K. T. Chen</name>
<affiliation wicri:level="1"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Chemistry, Wayne State University, Detroit, Michigan 48202</wicri:regionArea>
<wicri:noRegion>Michigan 48202</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Lim, E C" sort="Lim, E C" uniqKey="Lim E" first="E. C." last="Lim">E. C. Lim</name>
<affiliation wicri:level="1"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Chemistry, Wayne State University, Detroit, Michigan 48202</wicri:regionArea>
<wicri:noRegion>Michigan 48202</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Chemical Physics Letters</title>
<title level="j" type="abbrev">CPLETT</title>
<idno type="ISSN">0009-2614</idno>
<imprint><publisher>ELSEVIER</publisher>
<date type="published" when="1983">1983</date>
<biblScope unit="volume">100</biblScope>
<biblScope unit="issue">5</biblScope>
<biblScope unit="page" from="389">389</biblScope>
<biblScope unit="page" to="392">392</biblScope>
</imprint>
<idno type="ISSN">0009-2614</idno>
</series>
<idno type="istex">75471EDB10C1B0717A6956F64259C9AC1D153C02</idno>
<idno type="DOI">10.1016/0009-2614(83)87335-7</idno>
<idno type="PII">0009-2614(83)87335-7</idno>
<idno type="ArticleID">87335</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0009-2614</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass></textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">The rotational-temperature dependence of the energy-resolved fluorescence, combined with the calculated level density, indicates that the large variations in the rate of the intramolecular vibrational relaxation over a small excess energy in S1 perylene is due to the fluctuations in the density of accessible vibrational levels, resulting from the vibrational selection rules for second-order Coriolis coupling.</div>
</front>
</TEI>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Ticri/CIDE/explor/OcrV1/Data/Main/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 004235 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Merge/biblio.hfd -nk 004235 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Ticri/CIDE |area= OcrV1 |flux= Main |étape= Merge |type= RBID |clé= ISTEX:75471EDB10C1B0717A6956F64259C9AC1D153C02 |texte= Coriolis effects on “intermediate case” of intramolecular vibrational relaxation: Rotational-temperature dependence of energy- resolved fluorescence from jet-cooled perylene with 776–975 cm−1 excess energies }}
This area was generated with Dilib version V0.6.32. |