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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Reduction of oxygen catalyzed by nickel diphosphine complexes with positioned pendant amines
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Reduction of oxygen catalyzed by nickel diphosphine complexes with positioned pendant amines

机译:带有定位的侧链胺的镍二膦配合物催化的氧还原

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摘要

Nickel(II) bis(diphosphine) complexes that contain positioned bases in the second coordination sphere have been found to catalyze the reduction of O-2 with H-2 to selectively form water. The complexes also serve as electrocatalysts for the reduction of O-2 with the addition of a weak acid. In contrast, a closely related nickel diphosphine complex without the positioned bases is catalytically inactive for O-2 reduction. These results indicate that pendant bases in synthetic catalysts for O-2 reduction can play a similar role to proton relays in enzymes, and that such relays should be considered in the design of catalysts for multi-electron and multi-proton reactions.
机译:已发现在第二配位球中含有定位碱基的镍(II)双(二膦)配合物可催化H-2还原O-2,从而选择性地形成水。配合物还可以作为电催化剂,通过添加弱酸来还原O-2。相反,没有相关碱基的紧密相关的镍二膦配合物对于O-2还原具有催化活性。这些结果表明,用于O-2还原的合成催化剂中的侧基可与酶中的质子继电器起相似的作用,并且在设计用于多电子和多质子反应的催化剂时应考虑使用此类继电器。

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