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作 者:张华[1] 王国雄[2] 季峰 王谷丰[2] 王德 胡宏纹[2] 姚天扬[2]
机构地区:[1]北京大学化学与分子工程学院智能材料研究中心 [2]南京大学化学系
出 处:《高等学校化学学报》1998年第3期331-334,共4页Chemical Journal of Chinese Universities
摘 要:测定了双臂套索冠醚双核铜(Ⅱ)配合物[Cu2L(OH)](ClO4)3Me2CO(L=N,N′-二(8-喹啉甲基)-1,4,10,13-四氧-7,16-二氮环八环)的变温磁化率(4~300K),所加场强为5.0×105A/m.拟合了变温磁化率数据,得到J=-279.4cm-1;加上分子场校正后,得J=-257.7cm-1,Zj′=-30.1cm-1.拟合结果表明,分子间存在反铁磁性交换作用,而分子内的磁交换(J<500cm-1)还未大到使其反铁磁性交换作用变为抗磁性.用自旋倾斜体系解释了其反常的χm-H图.晶体结构和Cu2+3d轨道的分析表明,磁交换作用是通过OH桥进行的.比较了另外2个类似的双核铜(Ⅱ)大环OH桥联配合物。The variable temperature(4 ̄300 K) magnetic susceptibility of binuclear copper(Ⅱ) complex of the bibracchial lariat ether Cu 2L(OH) (ClO 4) 3Me 2CO(L= N,N ′ bis(8 quinolylmethyl) 1,4,10,13 tetraoxa 7,16 diazacyclooctadecane) (1) was measured in an appropriate magnetic field of 500 000 A/m. The strongly antiferromagnetic interaction constants are as follows: J =-257.7 cm -1 , Zj′ =-30.1 cm -1 . It is shown that there is an antiferromagnetic interaction between molecules. The | J | value (<500 cm -1 ) is not large enough to lead to the diamagnetic coupling. The plot of χ m H , which is different from the normal plot of χ m H , is explained through the spin canting phenomenon. By analyzing the crystal structure of the complex and 3 d orbitals of two Cu 2+ cations, we suggest that the exchange path is through OH bridge. Compared with the other two analogous binuclear copper(Ⅱ) complexes coordinated by macrocycle ligand and bridged by OH, we analyzed the correlation between J value and the overlap of orbitals.
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