The absorption and fluorescence spectra of 2-[4-(dimethylamino)phenyl]-3-hydroxy-4H-chromene-4-one in benzene or toluene and in the presence of methanol (proton donor) or the highly polar dimethylsulfoxide (proton acceptor) were measured and analyzed from the point of view of the potential influence
Heavy-atom effect on emission from free and hydrogen-bonded complexes of excited 1,2,3,4-tetrahydroquinoline
✍ Scribed by P. Jana; G.K. Mallik; T. Ganguly; S.B. Banerjee
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 386 KB
- Volume
- 172
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
At 77 K, 1,2,3+tetrahydroquinoline (THQ) forms a simple hydrogen bond with ethanol while at 300 K, a hydrogen-bonded ion pair is formed. Both intermolecular intersystem crossing and intramolecular singlet-triplet energy-transfer processes induced by heavy-atomquencher dihalobenzenes are weak in ethanol at 300 K, and the overall fluorescence quenching is smaller in ethanol than in cyclohexane. In methylcyclohexane rigid glass at 77 K, a triplet-state exciplex is formed between THQ and dihalobenzenes.
In ethanol medium at 77 K, there is no reaction between the THQ-ethanol exciplex and dihalobcnzenes involving the triplet state of THQ.
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