The dynamic nature of the quenching of the fluorescence of 1,4\_amino-and hydroxy-substituted 9, IO-anthraquinone, with benzene, alkylbenzenes and other aryl hydrocarbons as quenchers, indicates formation of exciplexes, where charge transfer (CT) occurs from the S, (quencher) to the S, (fluoropliore
Excited state pK*a values of naphthylamines: proton-induced fluorescence quenching
✍ Scribed by Kinzo Tsutsumi; Haruo Shizuka
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- English
- Weight
- 390 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
The dynamic bahavior of the excited singlet of naphthylamines involving proton-induced quenching in a sulfulic acidwater mixture has been studied by means of fluorometry and nanosecond time resolved spectroscopy. A significant tluorcsceace quenching of neutral (Y-and b-naphthylamines induced by protons was observed: 'k q = 8.9 (20.3) X 10' M-' s-l and Ikq = 3.3 (kO.2) X lo8 M-' s-l at 300 K, respectively. On the basis of kinetic analyses. the corrected values of pK,* were determined fo be -1.0 (20.2) and -0.8 (kO.1) for Q-and p-amines, respectively.
The isotope effect on the quenching was also examined.
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## Abstract An excited‐state proton transfer (ESPT) process, induced by both intermolecular and intramolecular hydrogen‐bonding interactions, is proposed to account for the fluorescence sensing mechanism of a fluoride chemosensor, phenyl‐1__H__‐anthra(1,2‐__d__)imidazole‐6,11‐dione. The time‐depend