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首页> 外文期刊>Bulletin of the Korean Chemical Society >Studies on Reactions of a Nickel Complex of a New Completely Conjugated Macrocyclic Ligand
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Studies on Reactions of a Nickel Complex of a New Completely Conjugated Macrocyclic Ligand

机译:新型完全共轭的大环配体镍配合物的反应研究

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The macrocyclic nickel complex of the molecular formula[Ni(C32H26N4)] has been synthesized from the template condensation reaction between 1-benzoylacetone and o-phenylenediamine in the presence of nickel acetate. Protonation and deuterium exchange reactions of the demetallated macrocyclic ligand and the nickel complex have been carried out. The infrared, electronic and proton magnetic resonance spectral data of both compounds are compared and discussed; protonation of the macrocyclic ligand take place at the nitrogen atoms and all the amine protons undergo very rapid deuterium exchange while the methine protons undergo very slow exchange. On the other hand, protonation of the nickel complex occurs at the nitrogen atoms and only amine protons undergo rapid deuterium exchange. Protonation and deprotonation of the nickel complexes proceed reversibly.
机译:分子式[Ni(C32H26N4)]的大环镍配合物是由1-苯甲酰丙酮与邻苯二胺在乙酸镍存在下的模板缩合反应合成的。已进行了脱金属大环配体和镍络合物的质子化和氘交换反应。比较和讨论了这两种化合物的红外,电子和质子磁共振光谱数据。大环配体的质子化发生在氮原子上,所有胺质子经历非常快速的氘交换,而次甲基质子经历非常缓慢的交换。另一方面,镍络合物的质子化发生在氮原子上,只有胺质子发生快速氘交换。镍配合物的质子化和去质子化可逆地进行。

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