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A Reversible Phase Transition of 2D Coordination Layers by B–H∙∙∙Cu(II) Interactions in a Coordination Polymer

机译:配位聚合物中B–H∙∙∙Cu(II)相互作用引起的二维配位层的可逆相变

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摘要

Materials that combine flexibility and open metal sites are crucial for myriad applications. In this article, we report a 2D coordination polymer (CP) assembled from CuII ions and a flexible meta-carborane-based linker [Cu2(L1)2(Solv)2]•xSolv (1-DMA, 1-DMF, and 1-MeOH; L1: 1,7-di(4-carboxyphenyl)-1,7-dicarba-closo-dodecaborane). 1-DMF undergoes an unusual example of reversible phase transition on solvent treatment (i.e., MeOH and CH2Cl2). Solvent exchange, followed by thermal activation provided a new porous phase that exhibits an estimated Brunauer-Emmett-Teller (BET) surface area of 301 m2 g−1 and is capable of a CO2 uptake of 41 cm3 g−1. The transformation is reversible and 1-DMF is reformed on addition of DMF to the porous phase. We provide evidence for the reversible process being the result of the formation/cleavage of weak but attractive B–H∙∙∙Cu interactions by a combination of single-crystal (SCXRD), powder (PXRD) X-ray diffraction, Raman spectroscopy, and DFT calculations.
机译:结合了灵活性和开放金属部位的材料对于多种应用至关重要。在本文中,我们报告了一种由CuII离子和一种柔性的基于间碳环的连接基[Cu2(L1)2(Solv)2]•xSolv(1-DMA,1-DMF和1 -MeOH; L 1:1,7-二(4-羧苯基)-1,7-二氨基甲酰-叔十二硼烷。 1-DMF在溶剂处理(即MeOH和CH2Cl2)上经历了不寻常的可逆相变示例。进行溶剂交换,然后进行热活化,提供了一种新的多孔相,该相具有约301 m 2 g -1 的Brunauer-Emmett-Teller(BET)表面积。的二氧化碳吸收量为41 cm 3 g -1 。该转化是可逆的,并且在向多孔相中添加DMF时可以重新形成1-DMF。我们通过单晶(SCXRD),粉末(PXRD)X射线衍射,拉曼光谱分析,结合形成弱的但有吸引力的B–H∙∙∙Cu相互作用的结果,证明了可逆过程的发生。和DFT计算。

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