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首页> 外文期刊>Zeitschrift fur Anorganische und Allgemeine Chemie >Copper(I) and Iron(II) Complexes of a Novel Tris(pyridyl)ethane-Derived N_4 Ligand: Aspects of Redox Behaviour and Bioinorganic Physicochemistry
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Copper(I) and Iron(II) Complexes of a Novel Tris(pyridyl)ethane-Derived N_4 Ligand: Aspects of Redox Behaviour and Bioinorganic Physicochemistry

机译:新型三(吡啶基)乙烷衍生的N_4配体的铜(I)和铁(II)配合物:氧化还原行为和生物无机物理化学的方面

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摘要

The N_4 ligand 1-{6-[1,1-bis(pyridin-2-yl)ethyl]pyridin-2- yl}-N,N-dimethylmethanamine (L) is presented. It has been used to obtain the copper(I) complex [CuL(MeCN)]PF_6 and the iron(II) complex [Fe(CN)_2L]. Aerobic oxidation of the copper(I) complex is unspecific at room temperature. Anaerobic oxidation in solution, which is very sluggish, occurs with formation of the copper(II) complex [Cu~(II)FL]PF_6, suggesting concomitant hydrolysis of hexafluorophosphate initiated by traces of water. The iron(II) complex adsorbed at a TiO_2 surface is an efficient photosensitiser of the support. Photoelectrochemical photocurrent switching (PEPS), which can be initiated by changing the electrochemical potential and photon energy, is very pronounced. The construction of a simple photoelectrochemical NOR logic gate has been demonstrated.
机译:提出了N_4配体1- {6- [1,1-双(吡啶-2-基)乙基]吡啶-2-基} -N,N-二甲基甲胺(L)。它已用于获得铜(I)络合物[CuL(MeCN)] PF_6和铁(II)络合物[Fe(CN)_2L]。铜(I)配合物的好氧氧化在室温下没有特异性。溶液中的厌氧氧化反应非常缓慢,会形成铜(II)络合物[Cu〜(II)FL] PF_6,这表明由微量水引发的六氟磷酸盐的伴随水解。吸附在TiO_2表面的铁(II)络合物是载体的有效光敏剂。可以通过改变电化学势和光子能量来启动的光电化学光电流切换(PEPS)非常显着。已经证明了简单的光电化学NOR逻辑门的构造。

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