Self-Assembly of 1D Double-Chain and 3D Diamondoid Networks of Lanthanide Coordination Polymers through In Situ-Generated Ligands: High-Pressure CO(2) Adsorption and Photoluminescence Properties

通过原位生成配体自组装镧系配位聚合物的一维双链和三维金刚石型网络:高压CO₂吸附和光致发光性能

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Abstract

Two new lanthanide-based coordination polymers, [Sm(2)(bzz)(ben)(6)(H(2)O)(3)]·0.5H(2)O (1) and [Eu(bbz)(ben)(3)] (2), were synthesized and characterized. The described products were formed from in situ-generated benzoate (ben) and N'-benzoylbenzohydrazide (bbz) ligands, which were the products of transformation of originally added benzhydrazide (bzz) under hydrothermal conditions. Compound 1 exhibits a one-dimensional (1D) double-chain structure built up from the connection of the central Sm(3+) ions with a mixture of bzz and ben ligands. On the other hand, 2 features a 3D network with a 4-connected (6(6)) dia topology constructed from dinuclear [Eu(2)(ben)(6)] secondary building units and bbz linkers. High-pressure CO(2) sorption studies of activated 1 show that maximum uptake increases to exceptionally high values of 376.7 cm(3) g(-1) (42.5 wt%) under a pressure of 50 bar at 298 K with good recyclability. Meanwhile, 2 shows a typical red emission in the solid state at room temperature with the decay lifetime of 1.2 ms.

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