Kaneko Wakako, Ohba Masaaki, Kitagawa Susumu
Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto, Japan.
J Am Chem Soc. 2007 Nov 7;129(44):13706-12. doi: 10.1021/ja074915q. Epub 2007 Oct 11.
Structural flexibility is a remarkable characteristic of coordination polymers and significant for the attainment of environmental responsivity. We have prepared a 2D cyanide-bridged MnIICrIII coordination polymer, [Mn(NNdmenH)(H2O)][Cr(CN)6].H2O (1; NNdmen = N,N-dimethylethylenediamine), with sophisticatedly arranged removable water coligands. The compound clearly showed a reversible single-crystal-to-single-crystal transformation between the 2D sheet and a 3D pillared-sheet framework of dehydrated [Mn(NNdmenH)][Cr(CN)6] (1a). The structural change was reversible and accompanied with generation/cleavage of CN-Mn bonds between 2D sheets by dehydration/hydration. Compounds 1 and 1a also exhibited a ferrimagnetic ordering at 35.2 and 60.4 K, respectively, and the magnetic characteristics were reversibly converted by guest adsorption/desorption. In addition, the dehydrated 1a demonstrated a size-selective solvent adsorption linking chemi- and physisorption processes and shrinkage/expansion of its framework. The flexible magnetic framework incorporating removable coligands delivered multifunctions with chemical response.
结构灵活性是配位聚合物的一个显著特征,对于实现环境响应性具有重要意义。我们制备了一种二维氰基桥联的MnIIICrIII配位聚合物[Mn(NNdmenH)(H2O)][Cr(CN)6].H2O(1;NNdmen = N,N-二甲基乙二胺),其具有排列精巧的可去除水配体。该化合物在二维片层与脱水后的[Mn(NNdmenH)][Cr(CN)6](1a)的三维柱状片层框架之间清晰地展示了可逆的单晶到单晶转变。结构变化是可逆的,并且伴随着二维片层之间通过脱水/水合作用产生/断裂CN-Mn键。化合物1和1a分别在35.2 K和60.4 K表现出亚铁磁有序,并且磁特性通过客体吸附/解吸作用可逆地转变。此外,脱水后的1a展示了连接化学吸附和物理吸附过程的尺寸选择性溶剂吸附以及其框架的收缩/膨胀。包含可去除配体的柔性磁性框架展现出具有化学反应性的多功能性。