首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Water-induced reversible structural phase transformation with chromotropism in metal supramolecular frameworks containing aminopyrazine and sulfate anions
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Water-induced reversible structural phase transformation with chromotropism in metal supramolecular frameworks containing aminopyrazine and sulfate anions

机译:在含氨基吡嗪和硫酸根阴离子的金属超分子骨架中水致变色的水诱导可逆结构相变

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Three new supramolecular metal-coordination architectures [M(H _2O)_4(ampyz)_2][M(H_2O) _6](SO_4)_2(H_2O)_2 (M = Co (1), Fe (2), and mixed Co/Fe (3); ampyz = 2-aminopyrazine) and a Cd(ii) coordination polymer [Cd(ampyz)(H_2O)_2(SO _4)]_n(H_2O)_n (4) were synthesized by layered diffusion and structurally characterized. Compounds 1-3 are isomorphous. Monomeric complex units [M(H_2O)_4(ampyz)_2] ~(2+) are assembled by intermolecular hydrogen bonding and π-π stacking via ampyz moieties to build 2D sheets. These layers are linked by intermolecular hydrogen bonding via ampyz ligand, [M(H_2O) _6]~(2+) unit, sulfate anion and lattice and coordinated water molecules to stabilize 3D supramolecular structure. Compound 4 shows a 2D coordination network where the sulfato connector and the bridging ampyz link Cd(ii) ions. Lattice water molecules are filled in between the layers via the hydrogen bonds stabilizing 3D supramolecular network of 4. Interestingly, compounds 1-3 exhibit water-induced reversible crystal-to-amorphous transformations with chromotropism and compound 4 also shows water-induced reversible structural phase transformation confirmed by spectroscopic techniques, elemental analyses, TGA, and XRPD. These results demonstrate the significant role between coordination bridges and weaker intermolecular interactions for the structural conversion even though 1-3 lack coordination bridges for the maintenance of their structures, however, the weak intermolecular interactions, especially hydrogen bonding, play a key role to the recovery of the crystalline phase.
机译:三种新的超分子金属配位体系结构[M(H _2O)_4(ampyz)_2] [M(H_2O)_6](SO_4)_2(H_2O)_2(M = Co(1),Fe(2)和混合Co / Fe(3); ampyz = 2-aminopyrazine)和Cd(ii)配位聚合物[Cd(ampyz)(H_2O)_2(SO _4)] _ n(H_2O)_n(4)合成并进行结构表征。化合物1-3是同构的。单体复合单元[M(H_2O)_4(ampyz)_2]〜(2+)通过分子间氢键键合和通过ampyz部分进行π-π堆积来构建2D薄片。这些层通过氨吡唑配体,[M(H_2O)_6]〜(2+)单元,硫酸根阴离子和晶格以及配位的水分子通过分子间氢键连接,以稳定3D超分子结构。化合物4显示了2D配位网络,其中的sulfato连接器和架桥的ampyz连接Cd(ii)离子。晶格水分子通过稳定4的3D超分子网络通过氢键填充在各层之间。有趣的是,化合物1-3表现出水致色性可逆的晶体到非晶转变,化合物4也显示出水致可逆的结构相光谱技术,元素分析,TGA和XRPD证实了转化。这些结果表明,即使1-3缺乏用于维持其结构的配位桥,配位桥和较弱的分子间相互作用对于结构转化也具有重要作用,但是,弱的分子间相互作用(尤其是氢键)在回收中起关键作用。结晶相。

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