1977
DOI: 10.1016/0009-2614(77)80074-2
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Triplet state of rhodamine dyes and its role in production of intermediates

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Cited by 58 publications
(44 citation statements)
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“…One is to examine the alternative de-excitation processes: intersystem crossing (ISC) to a triplet state and internal conversion back to the ground electronic state. The former is low in solution, estimated at less than 0.01 yield [88]. Kappes and coworkers have recently reported that gaseous rhodamine 6G cations have a long-lived triplet state, however they did not suggest an ISC yield higher than the solution-phase value.…”
Section: Discussionmentioning
confidence: 95%
“…One is to examine the alternative de-excitation processes: intersystem crossing (ISC) to a triplet state and internal conversion back to the ground electronic state. The former is low in solution, estimated at less than 0.01 yield [88]. Kappes and coworkers have recently reported that gaseous rhodamine 6G cations have a long-lived triplet state, however they did not suggest an ISC yield higher than the solution-phase value.…”
Section: Discussionmentioning
confidence: 95%
“…If there is any triplet-state absorption of the excitation laser light, the thermal energy coming out by the relaxation from the higher excited triplet state should also contribute to the thermal lens signal. The triplet states of Rhodamine B have been studied in aqueous and alcohol solutions by means of flash photolysis by Korobov et al 13 Their studies showed negligible, or no, T-T absorption for the wavelengths 514 nm and 532 nm, whereas the T-T absorption spectra overlaps the singlet fluorescence. Thus the influence of T-T absorption at the pump wavelengths used in our studies could be safely neglected.…”
Section: Resultsmentioning
confidence: 99%
“…It is noteworthy that under the conditions of our experiments with cw excitation of dye solutions the lifetime of the triplet state is much less than the duration of the modulated cw laser excitation. In this case, the concentration of triplet molecules is associated with the concentration of singlet excited molecules (S*) by the expression 13 of the triplet and singlet excited states, respectively, and φT is the quantum yield of the intersystem crossing. Hence, a slowly rising pump light pulse would transfer most of the molecules to the triplet state.…”
Section: Resultsmentioning
confidence: 99%
“…The formation of Cu(I) was assisted more efficiently by EY where the best yield for 3a was observed. The absence of 3a was noticed when R6G was used (Table 1, entry 9), attributed to two possible reasons: (i) inability to form Cu(I) from Cu(II) due to the negligible intersystem crossing quantum yield (F ISC ¼ 0.002), 26 or (ii) absence of free carboxyl groups which could act as ligands of the catalytically active cations. 27 Then, other Cu(II) sources such as Cu(NO 3 ) 2 , Cu(OAc) 2 , and CuCl 2 were used (Table 1, entries 11-13 respectively).…”
Section: Resultsmentioning
confidence: 99%