Department of Chemistry, University College of Science, University of Calcutta, 92, A.P.C. Road, Kolkata-700 009, India.
Inorg Chem. 2013 Feb 4;52(3):1640-9. doi: 10.1021/ic302548z. Epub 2013 Jan 17.
Two new polynuclear manganese(II) complexes Mn(dptz)(N(3))(2) (1) and Mn(azpy)(N(3))(2) (2) (where dptz = dipyridyl-tetrazine and azpy = 4,4'-azobis(pyridine)) have been synthesized by self-assembly of the ligand azide, together with dptz and azpy as secondary spacers. The compounds are characterized by single-crystal X-ray diffraction analyses and variable-temperature magnetic measurements. The structural analyses reveal that in complex 1, which is the first reported Mn(II) complex with the ligand dptz, two μ(1,3) bridging azides connect neighboring manganese ions in a zigzag manner to generate a neutral two-dimensional (2D) sheet which is further connected by the dptz ligands to form a three-dimensional (3D) framework. By contrast, complex 2 contains dimeric Mn(2)(μ(1,1)-N(3))(2) fragments linked to four identical motifs by means of four single μ(1,3)-N(3) bridges, that generates a neutral 2D Mn(II)-azide sheet which is further interconnected by azpy ligands to neighboring manganese ions forming an unprecedented 3D network. Variable-temperature (2-300 K) magnetic susceptibility measurements show the presence of predominantly antiferromagnetic coupling for both complexes that has been reproduced with a regular antiferromagnetic S = 5/2 chain (J) with interchain interactions (j) modeled with the molecular field approximation with J = -7.1 cm(-1) and j' = -0.8 cm(-1) for 1 and J = -4.2 cm(-1) and j' = 0.1 cm(-1) for 2.
两个新的多核锰(II)配合物[Mn(dptz)(N(3))(2)](n)(1)和[Mn(azpy)(N(3))(2)](n)(2)(其中 dptz = 二吡啶-四嗪和 azpy = 4,4'-偶氮吡啶)已通过配体叠氮化物与 dptz 和 azpy 作为二级间隔物的自组装合成。这些化合物通过单晶 X 射线衍射分析和变温磁测量进行了表征。结构分析表明,在配合物 1 中,这是第一个报道的具有配体 dptz 的 Mn(II)配合物,两个μ(1,3)桥接叠氮化物以之字形方式连接相邻的锰离子,生成中性二维(2D)薄片,然后由 dptz 配体进一步连接形成三维(3D)骨架。相比之下,配合物 2 包含二聚体[Mn(2)(μ(1,1)-N(3))(2)](2+)片段,通过四个单μ(1,3)-N(3)桥连接到四个相同的基序,生成中性 2D Mn(II)-叠氮化物薄片,然后通过 azpy 配体与相邻的锰离子进一步相互连接,形成一个前所未有的 3D 网络。变温(2-300 K)磁化率测量表明,两个配合物中都存在主要的反铁磁耦合,这是通过用分子场近似模拟的具有链间相互作用的规则反铁磁 S = 5/2 链(J)来重现的,对于 1,J = -7.1 cm(-1)和 j' = -0.8 cm(-1),对于 2,J = -4.2 cm(-1)和 j' = 0.1 cm(-1)。