Two novel 3D metalâorganic frameworks, [ML]n (M = Co, 1; Mn, 2) were successfully prepared in solvothermal conditions using 3,3â²-dimethoxy-4,4â²-biphenyldicarboxylic acid (H2L) as the ligand. X-Ray crystallography analysis reveals that MOF 1 crystallizes in the monoclinic system, space group P21/c in contrast to MOF 2 in the tetragonal system, space group I. MOF 1 contains an elongated [CoO6] octahedron with two bound methoxy groups in the trans position, whereas MOF 2 has a compressed [MnO6] octahedron with two coordinated methoxy groups in the cis arrangement. The ligand L shows a novel bis(tridentate) bridging coordination mode. MOF 1 exhibits a 3D framework with CdSO4 (cds) topology consisting of two different nodes and good thermal stability (313 °C). MOF 2 is a doubly interpenetrated 3D α-Po framework with a higher thermal stability (368 °C). The study of magnetic properties in the temperature range of 1.8â300 K shows the occurrence of weak ferromagnetic interactions (J = 0.15 K) between the high-spin Co(II) ions in 1, but a weak antiferromagnetic coupling (J = â0.15 cmâ1) between Mn(II) ions in 2 due to the syn-anti carboxylate bridge.
以 3,3â²-二甲氧基-4,4â²-
联苯二
甲酸(H2L)为
配体,在溶热条件下成功制备了两种新型三维
金属有机框架 [ML]n(M = Co, 1; Mn, 2)。X 射线晶体学分析表明,MOF 1 晶型为单斜晶系,空间群为 P21/c,而 MOF 2 晶型为四方晶系,空间群为 I。MOF 1 包含一个拉长的[CoO6]八面体,其反式位置上有两个结合的甲氧基,而 MOF 2 则包含一个压缩的[MnO6]八面体,其顺式排列上有两个配位的甲氧基。
配体 L 显示出一种新颖的双(三叉)桥接配位模式。MOF 1 具有三维框架,CdSO4(cds)拓扑结构由两个不同的节点组成,具有良好的热稳定性(313 °C)。MOF 2 是一个双互穿三维δ-±-Po 框架,具有更高的热稳定性(368 °C)。在1.8â300 K温度范围内对磁性的研究表明,1中的高自旋Co(II)离子之间存在微弱的
铁磁相互作用(J = 0.15 K),而2中的Mn(II)离子之间则存在微弱的反
铁磁耦合(J = â0.15 cmâ1),这是由于合成-反
羧酸桥造成的。