Cu3(O2C16H23)6·1.2 C6H12的晶体结构和磁性行为。一个意想不到的结构和旋转挫折的例子

Rodolphe Clérac, F.Albert Cotton, Kim R Dunbar, Elizabeth A Hillard, Marina A Petrukhina, Bradley W Smucker
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引用次数: 5

摘要

以碱式碳酸铜CuCO3·Cu(OH)2为原料,与2,4,6-三异丙基苯甲酸反应制得一种羧酸铜。它含有三重对称的三核Cu36+核,每对铜原子由两个羧酸配体桥接。Cu···Cu分离度为3.131(3)Å,不存在直接成键。在1 000 G下1.8 ~ 380 K的磁化率数据表明,在10 ~ 50 K (μeff = 1.80 μB)之间存在双重态基态(G≈2.1)。在50 K以上,在380 K时,磁矩增加到2.69 μB,与自旋载流子之间存在反铁磁相互作用的等边三角形CuII体系的磁矩一致。
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Crystal structure and magnetic behavior of Cu3(O2C16H23)6·1.2 C6H12. An unexpected structure and an example of spin frustration

A copper(II) carboxylate has been obtained from the reaction of basic copper carbonate, CuCO3·Cu(OH)2, with 2,4,6-triisopropylbenzoic acid. It contains a trinuclear Cu36+ core with three-fold symmetry, with each pair of copper atoms bridged by two carboxylate ligands. The Cu···Cu separations are 3.131(3) Å, precluding any direct bonding. Magnetic susceptibility data from 1.8 to 380 K at 1 000 G indicate a doublet ground state, (g ≈ 2.1) between 10–50 K (μeff = 1.80 μB). Above 50 K, the magnetic moment increases to 2.69 μB at 380 K, as expected for an equilateral triangular system of CuII with antiferromagnetic interactions between spin carriers.

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