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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Self-Assembly of Metal-Organic Coordination Polymers Constructed from a Bent Dicarboxylate Ligand: Diversity of Coordination Modes, Structures, and Gas Adsorption
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Self-Assembly of Metal-Organic Coordination Polymers Constructed from a Bent Dicarboxylate Ligand: Diversity of Coordination Modes, Structures, and Gas Adsorption

机译:由弯曲的二羧酸配体构成的金属有机配位聚合物的自组装:配位模式,结构和气体吸附的多样性。

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We have synthesized five new metal-organic coordination polymers incorporating the bent ligand H(2)hfipbb [4,4'-(hexafluoroisopropylidene)bis(benzoic acid)) with different transition metal ions and co-ligands via solvothermal reactions to give [Zn-2(hfipbb)(2)(Py)2] center dot DMF (1), [Zn-2(hfipbb)(2)(4,4'-bipy)(H2O)] (2), [Zn-2(hfipbb)(2)(bpdab)] center dot 2DMF (3), [Cd-2(hfipbb)(2)(DMF)(2)] center dot 2DMF (4), and [Co(hfipbb)(dpp)] center dot MeOH (5) (py = pyridine, 4,4'-bipy = 4,4'-bipyridine, bpdab = 1,4-bis(4-pyridyl)-2,3-diaza-1,3-butadiene, dpp = 1,3-di(4-pyridyl)propane). Compound 1 displays a 2-fold 2D -> 2D parallel interpenetrated layer network with one-dimensional (1D) helical channels, while 3 exhibits a three-dimensional pillared helical-layer open framework of alpha-Po topology based upon binuclear paddlewheel units. In compounds 2 and 5, binuclear motifs with double carboxylate bridges are linked by hfipbb(2-) ligands into a 1D ribbon, which are further assembled into two-dimensional non-interpenetrated (4,4) layers via bipyridyl co-ligands. However, the different bridging modes of hfipbb(2-) ligands and the different disposition of the coordinated co-ligands around metal ions result in subtle differences in the final architecture. Thus, 2 is based on a binuclear cluster node, double-stranded hfipbb(2-) linkers, and single-stranded 4,4'-bipy linkers, while 5 is based on a binuclear cluster node and hfipbb(2-) and dpp linkers which are both double-stranded. Among these compounds, the Cd(II) complex 4 is possibly the most interesting because it represents a rare example in which metal centers are linked by carboxylate groups into infinite chains further joined together by hfipbb(2-) spacers to form a 2D network with tubular helical channels. All these coordination polymers exhibit low solvent-accessible volumes, Both 3 and 4 retain structural integrity and permanent microporosity upon evacuation of guest molecules, with hydrogen uptakes of 0.57 and 0.78 wt %, respectively, at 20 bar and 77 K.
机译:我们已经合成了五种新的金属有机配位聚合物,它们通过溶剂热反应与不同的过渡金属离子和共配体结合了弯曲的配体H(2)hfipbb [4,4'-(六氟异亚丙基)双(苯甲酸)) -2(hfipbb)(2)(Py)2]中心点DMF(1),[Zn-2(hfipbb)(2)(4,4'-bipy)(H2O)](2),[Zn-2 (hfipbb)(2)(bpdab)]中心点2DMF(3),[Cd-2(hfipbb)(2)(DMF)(2)]中心点2DMF(4)和[Co(hfipbb)(dpp) ]中心点MeOH(5)(py =吡啶,4,4'-联吡啶= 4,4'-联吡啶,bpdab = 1,4-双(4-吡啶基)-2,3-二氮杂-1,3-丁二烯,dpp = 1,3-二(4-吡啶基)丙烷)。化合物1显示具有一维(1D)螺旋通道的2折2D-> 2D平行互穿层网络,而化合物3显示基于双桨叶轮单元的alpha-Po拓扑的三维柱状螺旋层开放框架。在化合物2和5中,具有双羧酸盐桥的双核基元通过hfipbb(2-)配体连接到一维带中,该带进一步通过联吡啶共配体组装成二维非互穿(4,4)层。但是,hfipbb(2-)配体的不同桥接模式以及金属离子周围配位共配体的不同位置导致最终结构的细微差别。因此,2基于双核群集节点,双链hfipbb(2-)链接器和单链4,4'-bipy链接器,而5基于双核群集节点以及hfipbb(2-)和dpp都是双链的接头。在这些化合物中,Cd(II)络合物4可能是最有趣的,因为它代表了一个罕见的例子,其中金属中心通过羧酸根基团连接成无限链,并通过hfipbb(2-)间隔基进一步连接在一起,形成2D网络,管状螺旋形通道。所有这些配位聚合物均显示出低的溶剂可及体积,3和4保留了排空客体分子后的结构完整性和永久的微孔性,在20 bar和77 K下的氢吸收分别为0.57和0.78 wt%。

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