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超氧阴离子与铵离子通过形成氢键激活氧的电子转移还原反应。

Activation of electron-transfer reduction of oxygen by hydrogen bond formation of superoxide anion with ammonium ion.

作者信息

Ohkubo Kei, Kitaguchi Hironori, Fukuzumi Shunichi

机构信息

Department of Material and Life Science, Division of Advanced Science and Biotechnology, Graduate School of Engineering, Osaka University, SORST, Japan Science and Technology Agency (JST), Suita, Osaka 565-0871, Japan.

出版信息

J Phys Chem A. 2006 Oct 19;110(41):11613-6. doi: 10.1021/jp064115m.

Abstract

A hydrogen bond formed between the superoxide anion and the ammonium ion (NH4+) accelerates electron transfer from the C60 radical anion to oxygen significantly, whereas the tetra-n-butylammonium ion has no ability to form a hydrogen bond with the superoxidie anion, exhibiting no acceleration of the electron-transfer reduction of oxygen. The second-order rate constant of electron transfer from C60*- to O2 increases linearly with increasing concentration of NH4+. This indicates that O2*- produced in the electron transfer from C60 to O2 is stabilized by 1:1 complex formation between O2*- and NH4+. The 1:1 complex formed between O2*- and NH4+ was detected by ESR. The binding of O2*- with NH4+ results in a positive shift of the reduction potential of O2 with increasing concentration of NH4+, leading to the acceleration of electron transfer from C60*- to O2.

摘要

超氧阴离子与铵离子(NH4+)之间形成的氢键显著加速了电子从C60自由基阴离子向氧的转移,而四正丁基铵离子没有能力与超氧阴离子形成氢键,因此未表现出对氧的电子转移还原的加速作用。从C60*-到O2的电子转移二级速率常数随NH4+浓度的增加而线性增加。这表明在从C60到O2的电子转移中产生的O2*-通过O2*-与NH4+之间1:1络合物的形成而得以稳定。通过电子自旋共振(ESR)检测到了O2*-与NH4+形成的1:1络合物。随着NH4+浓度的增加,O2*-与NH4+的结合导致O2还原电位正向移动,从而加速了电子从C60*-向O2的转移。

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