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Studies of Pyridinyl-Containing 14-Membered Macrocyclic Copper(ii) Complexes

机译:含吡啶基的14元大环铜(ii)配合物的研究

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Six copper(ii) complexes of tetracoordinating, pyridinyl-containing 14-membered macrocycles with varying ratios of nitrogen and oxygen donor atoms were prepared and characterized by IR, UV/Vis, and EPR spectroscopy and cyclic voltammetry. A distorted tetragonal coordination of the copper center in the solid-state was established by X-ray crystallography for the tetraazamacrocyclic complex Cu-3 carrying a methoxybenzyl pendent arm and the trioxaaza complex Cu-6. The superoxide dismutase-like activity of the Cu~(II) complexes was investigated by inhibition of NADH oxidation. Although the UV/Vis and EPR spectra of the complexes were strongly affected when the coordinating nitrogen atoms were successively replaced by oxygen atoms, no significant change in their reactivity towards superoxide was observed. In all cases a 1:1 or 1:2 stoichiometry for the reaction with superoxide was found, with the exception of the methoxybenzyl-substituted tetraaza complex, which showed a low catalytic activity with a turnover number of about 10.
机译:制备了六种含氮原子和氧原子供体原子比例不同的四配位吡啶基含14元大环的铜(ii)配合物,并通过IR,UV / Vis和EPR光谱和循环伏安法进行了表征。通过X射线晶体学,确定了带有甲氧基苄基侧臂的四氮杂大环配合物Cu-3和三氧杂氮杂配合物Cu-6的固态铜中心的扭曲四方配位。通过抑制NADH的氧化来研究Cu〜(II)配合物的超氧化物歧化酶样活性。尽管当配位氮原子被氧原子连续取代时,配合物的UV / Vis和EPR光谱受到很大影响,但未观察到它们对超氧化物的反应性发生显着变化。在所有情况下,发现与超氧化物反应的化学计量比为1:1或1:2,但甲氧基苄基取代的四氮杂配合物除外,该配合物显示出较低的催化活性,周转数约为10。

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