科研之友
微信
新浪微博
Facebook
分享链接
摘要
Herein, the synthesis, crystal structure, and full characterization of a new soft porous coordination polymer (PCP) of ([Cu2(dmcapz)2(OH2)]DMF1.5)n (1) formulation, which is easily obtained in the reaction of CuX2 (X=Cl, NO3) salts with 3,5-dimethyl-4-carboxypyrazole (H2dmcapz) is present. Compound 1 shows a copper(II) dinuclear secondary building unit (SBU), which is supported by two pyrazolate bridges and an unprecedented H2O bridge. The dinuclear SBUs are further bridged by the carboxylate ligands to build a diamondoid porous network. The structural transformations taking place in 1 framework upon guest removal/uptake has been studied in detail. Indeed, the removal of the bridging water molecules gives rise to a metastable evacuated phase (1?b) that transforms into an extremely stable porous material (1?c) after freezing at liquid-nitrogen temperature. The soaking of 1?c into water allows the complete and instantaneous recover of the water-exchanged material (1?a%26apos;). Remarkably, 1?b and 1?c materials possess structural bistability, which results in the switchable adsorptive functions. Therefore, the gas-adsorption properties of both materials have been studied by means of single-component gas adsorption isotherms as well as by variable-temperature pulse-gas chromatography. Both materials present permanent porosity and selective gas-adsorption properties towards a variety of gases and vapors of environmental and industrial interest. Moreover, the flexible nature of the coordination network and the presence of highly active convergent open metal sites confer on these materials intriguing gas-adsorption properties with guest-triggered framework-breathing phenomena being observed. The plasticity of CuII metal center and its ability to form stable complexes with different coordination numbers is at the origin of the structural transformations and the selective-adsorption properties of the studied materials.
- 出版日期2012-10
