Correlation of singlet energies of aromatic hydrocarbons with the rates of protonation of their anion radicals
โ Scribed by Hahn Levanon; P. Neta; A.M. Trozzolo
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- English
- Weight
- 437 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
formation and protonatron of aromatrc anion radicals in 2-propanol were studred by kinetic spectrophotomctr:c pulse radiolysis. All polycychc hydrocarbons studied were found to react very rapidly wrth c;olv. Those with xlattvely h!gh elcctron affinity were also reduced by (CIls)&O-. The anion radicals formed uudcrgo protonation by direct reaction with the alcohol molecule. The rate constants for this protonation vary from =Z 6 X LO5 s-' for cis-stilbcne .md naphthalene down to 20 s-t for perylenc. The variations in rates arc discussed in terms of changes in siuglct cncrgy separation (GS, + Se). The logarithm of the protonation rate constant for alternant hydrocarbons I hnearly dcpcndcnt on A+,
๐ SIMILAR VOLUMES
1972: reoe1v.d In UK fw publication 2 Jan-1973) Aromatic radical anions react principally as reducing agent& or nucleophiles la,2 or combinations of these.
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