Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/40342
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dc.contributor.authorDas, Ranjan-
dc.contributor.authorMitra, Sivaprasad-
dc.contributor.authorNath, Debnarayan-
dc.contributor.authorMukherjee, Samaresh-
dc.date.accessioned2017-02-10T07:28:11Z-
dc.date.available2017-02-10T07:28:11Z-
dc.date.issued1995-11-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/40342-
dc.description850-856en_US
dc.description.abstractThe proton transfer processes of the ground and excited states of 4-methyl-2, 6-diacetylphenol (MAOH) have been investigated by means of absorption, emission, nanosecond and picosecond transient emission spectroscopy at different temperatures. The fluorescence quantum yields are found to be dependent on temperature, excitation energy and added base. Unlike 4-methyl-2, 6-diformylphenol (MFOH), MAOH shows a single fluorescence band at room temperature in dimethyl sulphoxide and N,N-dimethylformamide and at 77K it does not exhibit any phosphorescence emission. The fluorescence lifetime and decay. rates of MAOH are temperature dependent and are relatively faster than those of MFOH. The solute-solvent interaction appears to play an important role in the proton transfer reaction of MAOH.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.34A(11) [November 1995]en_US
dc.titleGround and excited state proton transfer of 4-methyl- 2,6-diacetylphenol in some highly polar aprotic solvents: Interaction with baseen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.34A(11) [November 1995]

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