Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21693
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dc.contributor.authorSingh, Anil K-
dc.contributor.authorHota, Prasanta K-
dc.date.accessioned2013-10-09T04:41:27Z-
dc.date.available2013-10-09T04:41:27Z-
dc.date.issued2003-09-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21693-
dc.description2048-2053en_US
dc.description.abstractWhile 3-(4-nitrophenyl ethenyl-E)-N-H indole is photochemically stable, and shows dramatically red-shifted solvatochromic fluorescence emission (λem 642 nm with λex 405 nm in acetonitrile), the corresponding p-aminophenyl derivative, 3-(4-amino phenyl ethenyl-E)-N-H indole undergoes photocyclodehydrogenation yielding a benzocarbazole photoproduct together with a moderately red-shifted fluorescence emission (λem 404/414 nm with λex 323 nm in acetonitrile).en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(09) [September 2003]en_US
dc.titlePhotoreactivity of donor- acceptor ethenesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(09) [September 2003]

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