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Metal-organic coordination frameworks based on mixed methylmalonate and 4,4′-bipiridine ligands: synthesis, crystal structure and magnetic properties

机译:基于丙二酸甲酯和4,4'-联吡啶配体的金属-有机配位框架:合成,晶体结构和磁性

摘要

Five new complexes of formulae [M2(4,4′-bpy)(Memal)2X2]n [M = Fe(III) (2), Mn(II) (3), Co(II) (4), Ni(II) (5) and Zn(II) (6), and X = Cl−/OH− (2) and H2O (3–6); 4,4′-bpy = 4,4′-bipyridine and Memal = methylmalonate dianion] have been synthesized by following the previously reported procedure for [Cu2(4,4′-bpy)(Memal)2(H2O)2]n (1). Moreover, two new phases of the Cu(II)/Memal/4,4′-bpy system, namely {[Cu(4,4′-bpy)2][Cu(4,4′-bpy)2(Memal)(NO3)(H2O)]}n·nNO3·3.5nH2O (7) and [Cu(4,4′-bpy)2(Memal)(H2O)]n·nH2O (8), were obtained by varying the synthetic conditions. They were all structurally characterized by single crystal X-ray diffraction, and the magnetic properties of 2–5, 7 and 8 were investigated in the temperature range 1.9–295 K. 1–6 are isomorphous compounds whose structure consists of square grids of metal ions linked through anti–syn carboxylate bridges that grow in the crystallographic ac plane. These layers are pillared along the b axis by bis-monodentate 4,4′-bpy ligands to afford a [4466]-sqp three-dimensional net. Ferro- (1 and 5) and antiferromagnetic (2–4) interactions between the metal ions are mediated by the carboxylate bridge in the anti–syn conformation, the bis-monodentate 4,4′-bpy ligand being unable to transmit a significant magnetic coupling. The values of the magnetic coupling (J) for 2–5 are −0.269(3), −0.225(2), −0.05 and +0.272(3) cm−1 respectively, the isotropic spin Hamiltonian being . Complexes 7 and 8 exhibit quite a different structure, as driven by the 4,4′-bpy groups. A square-grid of [Cu(4,4′-bpy)2]2n+n occurs in 7, which grows in the ab plane and is pillared through anti–syn carboxylate bridges from [Cu(Memal)(4,4′-bpy)2(NO3)(H2O)] units along the c axis to build up a [41263]-pcu net. Analysis of the magnetic data for this compound shows an overall antiferromagnetic behaviour with the coexistence of ferro- and antiferromagnetic interactions. The structure of 8 consists of linear chains of copper(II) running along the c axis, where aquabis(4,4′-bipyridine)copper(II) units are connected by bis(monodentate) methylmalonate ligands. A significant intrachain antiferromagnetic interaction is observed in 8 through the extended Cu–OCCCO–Cu exchange pathway [J = −1.38(1) cm−1]. The assembling role of the 4,4′-bpy coligand in 1–8 and in previous malonate-containing complexes is analyzed and discussed.
机译:五个新的式[M2(4,4'-bpy)(Memal)2X2] n [M = Fe(III)(2),Mn(II)(3),Co(II)(4),Ni( II)(5)和Zn(II)(6),X = Cl- / OH-(2)和H2O(3-6);按照先前报道的[Cu2(4,4'-bpy)(Memal)2(H2O)2] n(4,4'-bpy = 4,4'-联吡啶和Memal =丙二酸二甲酯二价)( 1)。此外,Cu(II)/ Memal / 4,4'-bpy系统的两个新阶段,即{[Cu(4,4'-bpy)2] [Cu(4,4'-bpy)2(Memal) (NO3)(H2O)]} n·nNO3·3.5nH2O(7)和[Cu(4,4'-bpy)2(Memal)(H2O)] n·nH2O(8)通过改变合成条件获得。它们的结构均通过单晶X射线衍射表征,在1.9–295 K的温度范围内研究了2–5、7和8的磁性。1–6是同构化合物,其结构由金属的方格子组成离子通过在晶体学ac平面中生长的抗Syn羧酸盐桥连接。这些层沿b轴由双单齿4,4'-bpy配体支撑,以提供[4466] -sqp三维网。金属离子之间的铁(1和5)和反铁磁性(2-4)相互作用是由反正构象中的羧酸盐桥介导的,双单齿4,4'-bpy配体无法传递大量的磁性耦合。 2–5的磁耦合(J)值分别为-0.269(3),-0.225(2),-0.05和+0.272(3)cm-1,各向同性自旋哈密顿量为。配合物7和8表现出完全不同的结构,这受4,4'-bpy基团的驱动。 [Cu(4,4'-bpy)2] 2n + n的方格出现在7中,该方格在ab平面中生长,并通过[Cu(Memal)(4,4' -bpy)2(NO3)(H2O)]单位沿c轴构建[41263] -pcu网络。该化合物的磁数据分析表明,总体反铁磁行为与铁磁和反铁磁相互作用同时存在。 8的结构由沿c轴延伸的铜(II)的线性链组成,其中aquabis(4,4'-bipyridine)copper(II)单元通过双(单齿)丙二酸甲酯配体连接。通过扩展的Cu–OCCCO–Cu交换途径,在8中观察到了显着的链内反铁磁相互作用[J = −1.38(1)cm-1]。分析和讨论了4,4'-bpy大肠菌素在1–8和以前含丙二酸酯的复合物中的组装作用。

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