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
โฆ LIBER โฆ
Intramolecular quenching of the excited singlet state of a naphthyl group by halogeno substituents
โ Scribed by R.Stephen Davidson; Roland Bonneau; Jacques Joussot-Dubien; Kenneth R. Trethewey
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- English
- Weight
- 238 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0009-2614
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## Abstract A C๏ฃฟOโbond cleavage of esters having a naphthyl group, NpCOโOR and RCOโONp (Np=ฮฑโ and ฮฒโnaphthyl (^ฮฑ^Np and ^ฮฒ^Np, respectively), R=Ph and Me), was found during the twoโcolor twoโlaser flash photolysis in acetonitrile. The C๏ฃฟOโbond cleavage occurred when NpCOโOR and RCOโONp were excited
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