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含烷基咪唑的三足配体铜(II)配合物的离子液体。

Ionic liquids from copper(II) complexes with alkylimidazole-containing tripodal ligands.

机构信息

Department of Chemistry, Graduate School of Science, Kobe University, Rokkodai, Nada, Hyogo 657-8501, Japan.

出版信息

Dalton Trans. 2013 Jul 28;42(28):10138-43. doi: 10.1039/c3dt50976a.

Abstract

Five-coordinate copper(II) complexes [Cu(L)Cl]X bearing alkylimidazole-containing tripodal ligands were prepared, where L = bis(2-dimethylaminoethyl)-((1-alkylimidazol-2-yl)methyl)amine and X = bis(trifluoromethanesulfonyl)amide (Tf2N) and PF6. The salts with hexyl ([1]X), propyl ([2]X), and methyl ([3]X) substituents in the ligand were prepared, of which [1]Tf2N and [2]Tf2N were ionic liquids with high viscosity at room temperature. X-ray crystal structure determination at low temperature revealed that the coordination geometry around the metal ion in [3]Tf2N was distorted trigonal bipyramidal, whereas that in [2]PF6 was close to square pyramidal. UV-vis absorption spectra of these salts were consistent with the coordination structures.

摘要

五配位的铜(II)配合物[Cu(L)Cl]X,其中 L 是双(2-二甲氨基乙基)-((1-烷基咪唑-2-基)甲基)胺,X 是双(三氟甲磺酰基)酰胺(Tf2N)和 PF6。在配体中具有己基([1]X)、丙基([2]X)和甲基([3]X)取代基的盐被制备,其中[1]Tf2N 和[2]Tf2N 是室温下具有高粘度的离子液体。低温下的 X 射线晶体结构测定表明,[3]Tf2N 中金属离子的配位几何形状为扭曲的三角双锥,而[2]PF6 则接近于四方锥。这些盐的紫外可见吸收光谱与配位结构一致。

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