Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46391
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dc.contributor.authorSarpal, Ranjit S-
dc.contributor.authorDogra, Sneh K-
dc.date.accessioned2019-03-22T07:26:15Z-
dc.date.available2019-03-22T07:26:15Z-
dc.date.issued1990-06-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46391-
dc.description535-540en_US
dc.description.abstractEffects of solvents on the absorption and fluorescence spectra of 5-hydroxy-1-naphthylamine and 4-hydroxy-l-naphthylamine have indicated that the absorbing and emitting states are the same. The long wavelength spectral band is due to 1A → 1La transition. The proto tropic species observed in the ground and excited singlet states are five and six respectively. The ground state precursor for the zwitterion is the monocation and it is an excited state phenomenon. The dianion of 5-hydroxy-l-naphthylamine and monoanion of 5-methoxy-l-naphthylamine are formed by the deprotonation of -OH group and - C- H bond respectively.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-A Vol.29A(06) [June 1990]en_US
dc.titleEffects of solvents and acid concentration on absorption and fluorescence spectra of 1,4- and 1,5-aminonaphtholsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.29A(06) [June 1990]

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