http://www.cnr.it/ontology/cnr/individuo/prodotto/ID50439
Photocyclization of trans-1-(1-naphthyl)-2-(3-hydroxyphenyl)ethene: evidence for adiabatic 1trans*->1cis* photoisomerization (Articolo in rivista)
- Type
- Label
- Photocyclization of trans-1-(1-naphthyl)-2-(3-hydroxyphenyl)ethene: evidence for adiabatic 1trans*->1cis* photoisomerization (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/b404308a (literal)
- Alternative label
P. Bortolus, G. Galiazzo, G. Gennari, I. Manet, G. Marconi, S. Monti (2004)
Photocyclization of trans-1-(1-naphthyl)-2-(3-hydroxyphenyl)ethene: evidence for adiabatic 1trans*->1cis* photoisomerization
in Photochemical & photobiological sciences (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- P. Bortolus, G. Galiazzo, G. Gennari, I. Manet, G. Marconi, S. Monti (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
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- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- I. Manet, G. Marconi, S. Monti: ISOF-CNR (literal)
- Titolo
- Photocyclization of trans-1-(1-naphthyl)-2-(3-hydroxyphenyl)ethene: evidence for adiabatic 1trans*->1cis* photoisomerization (literal)
- Abstract
- The photochemistry of trans- and cis-1-(1'-naphthyl)-2-(3-hydroxyphenyl) ethene in cyclohexane and acetonitrile was examined. In cyclohexane fluorescence is the main deactivation channel for the (1)trans* isomer while photocyclization is the main reaction of the (1)cis* isomer. The weighty formation of hydroxychrysene following one photon absorption by the trans isomer furnished evidence of an adiabatic (1)trans*-->(1)cis* isomerization. The photoreactivity data in acetonitrile indicated the influence of solvent polarity on the shape of the excited state surface. (literal)
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