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苄基紫精的还原电位:氧化/自由基氧化还原对的重要参考化合物。

The reduction potential of benzyl viologen: an important reference compound for oxidant/radical redox couples.

作者信息

Wardman P

机构信息

Cancer Research Campaign, Mount Vernon Hospital, Northwood, Middlesex, U.K.

出版信息

Free Radic Res Commun. 1991;14(1):57-67. doi: 10.3109/10715769109088942.

Abstract

Bipyridinium compounds such as the viologens (V2+) have been used extensively as redox indicators, but radical dimerization leads to reduction potentials of the oxidant/radical one-electron couple, E(V2+/V2+) varying with radical concentration: a particular problem with benzyl viologen. Pulse radiolysis has been used to characterize the one-electron transfer equilibria between methyl (MV2+) or benzyl (BV2+) viologen and a 2-nitroimidazole (misonidazole), and between methyl and benzyl viologens directly. Total radical concentrations were typically approximately 0.4 mumol dm-3 to minimize dimerization. Based on E(MV2+/MV2+) = -450 mV, a value of E(BV2+/BV2+) = -374 mV is now recommended. The implications for other 'reference' redox couples are discussed.

摘要

联吡啶化合物如紫精(V2+)已被广泛用作氧化还原指示剂,但自由基二聚化导致氧化剂/自由基单电子偶合的还原电位,即E(V2+/V2+)随自由基浓度而变化:这是苄基紫精的一个特殊问题。脉冲辐解已用于表征甲基紫精(MV2+)或苄基紫精(BV2+)与2-硝基咪唑(米索硝唑)之间以及甲基紫精和苄基紫精之间的单电子转移平衡。总自由基浓度通常约为0.4 μmol dm-3,以尽量减少二聚化。基于E(MV2+/MV2+) = -450 mV,现推荐E(BV2+/BV2+) = -374 mV的值。还讨论了对其他“参考”氧化还原偶合的影响。

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