Bulletin of the Chemical Society of Japan
Online ISSN : 1348-0634
Print ISSN : 0009-2673
ISSN-L : 0009-2673
Primary Processes in the Photoreduction of Acridine in Various Alcohols
Masao KoizumiYoshinori IkedaHiroshi Yamashita
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1968 Volume 41 Issue 5 Pages 1056-1063

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Abstract

The effect of the addition of biacetyl on the quantum yield of photoreduction of acridine in methanol, ethanol, n- and iso-propanol has been studied under the aerated and deaerated conditions. From the analysis of the results, the quantum yields for four mechanisms ΦMS(S means that a reactive state is singlet excited states, S*, and M denotes a molecular mechanism), ΦMS (R denotes a radical mechanism), ΦMT (T indicates that a reactive state is a state other than S* and T(π–π*), most likely T(n–π*) and ΦRT have been decided, assuming that oxygen does not deactivate T(n–π*). The values are
5&for methanol, & &Φ_M^S(0.027) & &Φ_R^S(0.039) & &Φ_M^T(0.006) & &Φ_R^T(0.057)
&for ethanol, & &Φ_M^S(0.043) & &Φ_R^S(0.067) & &Φ_M^T(0) & &Φ_R^T(0.019)
&for n-propanol, & &Φ_M^S(0.030) & &Φ_R^S(0.036) & &Φ_M^T(0) & &Φ_M^T(0.022)
&for isopropanol, & &Φ_M^S(0.03) & &Φ_R^S(0.058) & &Φ_M^T(0) & &Φ_R^T(0)
The quenching constants of biacetyl on the fluorescence of acridine have been found to agree with the ones on the reaction at S* in all alcohols; the rate constants approximate diffusion controlled. In addition it has been confirmed by a flash method that biacetyl does not attack the T(π–π*) nor the semi-reduced acridine; this justifies the present method of analysis.

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