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首页> 外文期刊>ChemPlusChem >Catalytic Oxygen Evolution from Manganese Complexes with an Oxidation-Resistant N,N,O-Donor Ligand
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Catalytic Oxygen Evolution from Manganese Complexes with an Oxidation-Resistant N,N,O-Donor Ligand

机译:用抗氧化N,N,O-供体配体的锰配合物的催化氧量进化

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摘要

There is great interest in developing Mn water-splitting catalysts due to their low cost, abundance, and relevance to the oxygen-evolving complex (OEC). Three ligands with highly donating pyridine alkoxide moieties, including 2-(pyridin-2-yl)propan-2-ol (pyalkH), 2,2-(pyridine-2,6-diyl)bis(propan-2-ol) (py-dialkH(2)), and 2-[(2,2-bipyridin)-6-yl]propan-2-ol (bipy-alkH), have been screened with Mn for oxygen-evolution catalysis. Complexes with the ligand bipy-alkH were shown to evolve O-2 when driven by Oxone (potassium peroxymonosulfate). The catalytic mixture generated from the precursor complex [Mn(bipy-alkH)Cl-2] retained activity in unbuffered solution beyond 160h.
机译:由于它们的低成本,丰度和与氧化复合物(OEC)的相关性,对开发Mn水分裂催化剂的兴趣非常兴趣。 三种配体,具有高度吡啶醇盐部分,包括2-(吡啶-2-基)丙烷-2-醇(PyalkH),2,2-(吡啶-2,6-二基)双(Propan-2-Ol)( 用MN筛选丙烷-2-醇(BiPy-AlkH),丙烷-2-醇(2))和2 - [(2,2-Biphyridin)-6-Y1],用于氧化催化。 当由赭石(过氧化钾硫酸钾)驱动时,显示与配体BiPy-AlkH的复合物。 从前体复合物[Mn(BiPy-AlkH)Cl-2产生的催化混合物在超过160h的不缓解溶液中保留活性。

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