Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/18481
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dc.contributor.authorRajendiran, N-
dc.contributor.authorRadha, N-
dc.contributor.authorSwaminathan, M-
dc.date.accessioned2013-05-29T04:40:36Z-
dc.date.available2013-05-29T04:40:36Z-
dc.date.issued2001-04-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/18481-
dc.description331-339en_US
dc.description.abstractA study of solvent and pH effects on absorption and fluorescence of 1,7- and 1,5-naphthalenediols has been carried out. The life-times of neutral and monoanionic forms of both naphthalenediols have been determined. Solvatochromic shift of 1,7-naphthalenediol (l,7ND) is different from that of 1,5-naphthalenediol (1,5ND) both in the ground and excited states. The difference is more in S1 state. In 1,5ND the -OH groups are α αʹ and placed symmetrically, but in 1,7ND the –OH groups are α, βʹ and their positions are not symmetrical. The large solvatochromic and Stoke's shifts are explained on the basis of the point group symmetry of naphthalenediols. The stretched sigmoidal fluorimetric titration curves obtained for the equilibrium between neutral form and monoanion of both NDs are analysed using Weller's steady state kinetics and lifetimes of the species. These curves meet only at the ground state pKa values. The excited state equilibrium constants determined from rate constants and by other methods are compared.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.40A(04) [April 2001]en_US
dc.titleSolvatochromism and proton transfer kinetics of 1,5- and 1,7-naphthalenediols in the excited singlet state: A study by electronic spectraen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.40A(04) [April 2001]

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