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首页> 外文期刊>Science of advanced materials >A Crystal Structures, Dielectric, and CO2-Adsorption Properties of One-Dimensional [Cu(II)(2)(Adamantane-1-carboxylate)(4)(pyrazine)](infinity) Coordination Polymers with Polar Ligands
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A Crystal Structures, Dielectric, and CO2-Adsorption Properties of One-Dimensional [Cu(II)(2)(Adamantane-1-carboxylate)(4)(pyrazine)](infinity) Coordination Polymers with Polar Ligands

机译:一维[Cu(II)(2)(金刚烷-1-羧酸盐)(4)(吡嗪)](无穷大)配位聚合物与极性配体的晶体结构,介电和CO2吸附特性

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摘要

Cu(II) binuclear coordination polymers of [Cu(II)(ADCOO)(4)(pz)](infinity) (1), [Cu(II)(ADCOO)(4)(F-pz)](infinity) (2), and [Cu(II)(Cl-ADCOO)(4)(pz)](infinity) (3) were prepared, where ADCOO, Cl-ADCOO, pz, and F-pz are adamantane-1-carboxylate, 3-chloroadamantane-1-carboxylate, pyrazine, and 2-fluoropyrazine, respectively. The Cu(II) binuclear units of [Cu(II)(ADCOO)(4)] and [Cu(II)(Cl-ADCOO)(4)] were formed by the four bridging ligands of ADCOO and Cl-ADCOO to the two Cu(II) ions, respectively, which were further connected by the axial bidentate ligands of pz or F-pz, to form one-dimensional (1D) coordination polymers. Although the 1D coordination polymers were observed in the typical structures of crystals 1, 2, and 3, the packing structure of polymer 3 was different from those of crystals 1 and 2. Three-dimensional (3D) interdigitated polymer arrays were observed in 1 and 2 as cubic crystal systems with the I-43d space group, whereas the two-dimensional array of 1D polymers of 3 was the same as that of the [Cu(II)(C6H5COO)(4)(pz)](infinity) crystal. The crystal structure of 2 was not affected by the introduction of a polar F group into the axial pz ligand, whereas the introduction of the Cl-substituent into the ADCOO ligand significantly modified the packing structure of the coordination polymers. The polar ligands of F-pz in 2 and Cl-ADCOO in 3 were static at 110 K according to X-ray crystal structural analyses. The absolute magnitude of the dielectric constants was decreased in the order of 3, 2, and 1, which is consistent with the dipole moments of the ligands. No CO2 gas adsorption-desorption processes were observed in crystals 1, 2, and 3 at 195 K. The 3D interdigitated polymer arrangements in 1 and 2, and the strong dipole-dipole interaction between Cl-ADCOO ligands, were not responsible for the structural changes in the CO2 gas adsorption-desorption.
机译:[Cu(II)(ADCOO)(4)(pz)](无穷)(1),[Cu(II)(ADCOO)(4)(F-pz)](无穷)的Cu(II)双核配位聚合物(2)和[Cu(II)(Cl-ADCOO)(4)(pz)](无穷大)(3)制备,其中ADCOO,Cl-ADCOO,pz和F-pz为金刚烷-1-羧酸分别是3-氯金刚烷-1-羧酸盐,吡嗪和2-氟吡嗪。 [Cu(II)(ADCOO)(4)]和[Cu(II)(Cl-ADCOO)(4)]的Cu(II)双核单元是由ADCOO和Cl-ADCOO的四个桥连配体形成的。两个分别通过pz或F-pz的轴向双齿配体进一步连接的Cu(II)离子形成一维(1D)配位聚合物。尽管在晶体1、2和3的典型结构中观察到1D配位聚合物,但聚合物3的堆积结构与晶体1和2的堆积结构不同。在晶体1和2中观察到三维(3D)叉指型聚合物阵列。 2是具有I-43d空间群的立方晶体系统,而3的1D聚合物的二维阵列与[Cu(II)(C6H5COO)(4)(pz)](无穷大)晶体相同。 2的晶体结构不受向轴向pz配体中引入极性F基团的影响,而将Cl取代基引入ADCOO配体中则显着改变了配位聚合物的堆积结构。根据X射线晶体结构分析,在2K中的F-pz和在3中的Cl-ADCOO的极性配体在110K下是静态的。介电常数的绝对值按3、2和1的顺序减小,这与配体的偶极矩一致。在195 K的晶体1、2和3中未观察到CO2气体的吸附-解吸过程。1和2中的3D叉指状聚合物排列以及Cl-ADCOO配体之间的强偶极-偶极相互作用对结构没有影响。二氧化碳气体吸附-解吸的变化。

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