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Trinuclear Cu(ii) complexes of a chiral N _6O _3 amine

机译:N _6O _3手性胺的三核Cu(ii)配合物

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摘要

Enantiopure trinuclear Cu(ii) complexes 3 and 4 of macrocyclic amine 1 derived from the 3 + 3 condensation of 2,6-diformyl-4-methylphenol and (1S,2S)-1,2-diaminocyclohexane have been synthesized and characterized by ESI MS and NMR spectroscopy. The X-ray crystal structures of both complexes have been determined. The structure of the chloride derivative 3 indicates unusual combination of distorted tetragonal bipyramidal, square pyramidal and square geometries of the three Cu(ii) ions bound by macrocycle 1. The acetate complex 4 also exhibits unsymmetrical trinuclear core with the bridging and terminal acetate anions. The complexation of Cu(ii) ions by macrocycle 1 has been studied using potentiometric methods and both protonation and binding constants of 1 have been determined. The distribution of the complex forms indicates cooperative binding of three metal ions by 1. The overall magnetic behaviour for 3 corresponds to an antiferromagnetically coupled triangular system. Compound 4 shows the presence of antiferromagnetic coupling (J = -74.9(1) cm ~(-1)) between the metal centers in equilateral triangular array.
机译:由ESI合成并表征了2,6-二甲酰基-4-甲基苯酚与(1S,2S)-1,2-二氨基环己烷的3 + 3缩合反应得到的大环胺1对映体三核Cu(ii)配合物3和4 MS和NMR光谱。已经确定了两种配合物的X射线晶体结构。氯化物衍生物3的结构表明大环1结合的三个Cu(ii)离子的扭曲的四边形双锥体,方形锥体和方形几何结构的异常组合。乙酸盐络合物4还显示具有桥联和末端乙酸根阴离子的不对称三核核。已使用电位法研究了大环1络合Cu(ii)离子的过程,并确定了质子化常数和结合常数1。复数形式的分布表明三个金属离子之间的协同键合为1。3的总体磁性能对应于反铁磁耦合的三角系统。化合物4显示在等边三角形阵列的金属中心之间存在反铁磁耦合(J = -74.9(1)cm〜(-1))。

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