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Synthesis and structural studies of two pyridine-armed reinforced cyclen chelators and their transition metal complexes

机译:两种吡啶武装的增强环素螯合剂及其过渡金属配合物的合成与结构研究

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摘要

Two novel pyridine pendant-armed macrocycles structurally reinforced by an ethyl bridge, either between adjacent nitrogens (for side-bridged) or non-adjacent nitrogens (for cross-bridged), have been synthesized and complexed with a range of transition metal ions (Co2+, Ni2+, Cu2+ and Zn2+). X-ray crystal structures of selected cross-bridged complexes were obtained which showed the characteristic cis-V configuration with potential labile cis binding sites. The complexes have been characterized by their electronic spectra and magnetic moments, which show the expected high spin divalent metal complex in most cases. Exceptions are the nickel side-bridged complex, which shows a mixture of high-spin and low spin, and the cobalt cross-bridged complex which has oxidized to cobalt(III). Cyclic voltammetry in acetonitrile was carried out to assess the potential future use of these complexes in oxidation catalysis. Selected complexes offer significant catalytic potential enhanced by the addition of the pyridyl arm to a reinforced cyclen backbone.
机译:合成了两个在相邻氮原子之间(对于侧桥)或在不相邻氮原子之间(对于跨桥)在结构上由乙基桥增强的新型吡啶侧链大环,并与一系列过渡金属离子(Co 2 + ,Ni 2 + ,Cu 2 + 和Zn 2 + )。获得选定的跨桥复合物的X射线晶体结构,其显示出具有潜在的不稳定顺式结合位点的特征性顺式-V构型。配合物的特征在于其电子光谱和磁矩,在大多数情况下显示出预期的高自旋二价金属配合物。例外的是镍侧桥复合物(显示出高自旋和低自旋的混合物)和钴交叉桥复合物(已氧化成钴(III))。乙腈中的循环伏安法用于评估这些络合物在氧化催化中的潜在未来用途。选定的配合物通过将吡啶基臂添加到增强的Cyclen主链上,提供了显着的催化潜力。

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