1979
DOI: 10.1016/0022-2313(79)90182-0
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Absorption and fluorescence spectra of methyl salicylate in the vapor phase

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1983
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Cited by 42 publications
(21 citation statements)
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“…Since then, a substantial literature has discussed MS dual fluorescence. [10][11][12][13][14][15][16][17][18][19][20][21] Also along the way, the different isomers of MS have received a) Electronic mail: blaisten@gmu.edu. different names.…”
Section: Introductionmentioning
confidence: 99%
“…Since then, a substantial literature has discussed MS dual fluorescence. [10][11][12][13][14][15][16][17][18][19][20][21] Also along the way, the different isomers of MS have received a) Electronic mail: blaisten@gmu.edu. different names.…”
Section: Introductionmentioning
confidence: 99%
“…The tautomeric forms of compounds under study appearing in solvents [7,[20][21][22][23] possess electric dipole moments showing large differences (see Table 2). It induces a retirement of large differences of the orientation energy of the excited normal, S 1 (LE), and tautomer, S 1 (PT), species, thus a non-equilibrium distribution of solvent polarization effects may occur, i.e., noted as inhomogeneous band broadening [6,30], red shift of the phosphorescence band maximum, difference in the band shape of fluorescence excitation and absorption spectra and as the intensity ratio changes I Fl (PT)/I Fl (LE) determined for different l exc or l det values.…”
Section: Discussionmentioning
confidence: 99%
“…Taking into consideration the results of our earlier spectroscopic studies [15,[17][18][19]37] and other authors [1][2][3][4][5][6][7][8][9][10][11][12][13]16,[20][21][22][23][24][25][26][27][28][29]38], we suppose that the molecules under study can appear as: keto rotamers a and b, zwitterionic and enolic tautomeric forms. Some of them already appear in the S 0 state, others are formed in a photoinduced proton-transfer reaction and appear in S 1 state only.…”
Section: Quantum Chemical Calculationmentioning
confidence: 99%
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