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晶态卤代(氰基)铜酸盐家族的离子热设计:结构多样性、固态发光及光催化性能

Ionothermal Design of Crystalline Halogeno(cyano)cuprate Family: Structure Diversity, Solid-State Luminescence, and Photocatalytic Performance.

作者信息

Zhang Ya-Li, Ding Rui, Li Shu-Ni, Jiang Yu-Cheng, Hu Man-Cheng, Zhai Quan-Guo

机构信息

Key Laboratory of Macromolecular Science of Shaanxi Province, School of Chemistry & Chemical Engineering, Shaanxi Normal University , Xi'an, Shaanxi 710062, China.

出版信息

Inorg Chem. 2017 Jun 19;56(12):7161-7174. doi: 10.1021/acs.inorgchem.7b00814. Epub 2017 May 31.

Abstract

A general preparative method for multifunctional halogeno(cyano)cuprate materials in ionic liquids is developed in this work. Under ionothermal conditions, alkylimidazolium-based ionic liquids serving as solvent, charge-compensating, and structure-directing agent, as well as reactant lead to 12 members of the novel hybrid halogeno(cyano)cuprate family with a general formula of [RRRIM][CuX(CN)] (RRRIM = alkylimidazolium cations, X = halide anions). X-ray single-crystal diffractions show that diverse inorganic halogeno(cyano)cuprate components vary from discrete complexes (1 and 2), one-dimensional (1D) chains (3-7), two-dimensional (2D) layer (8), to three-dimensional (3D) open frameworks (9-12). 1 and 2 are of zero-dimensional discrete structures containing triangular [CuX] anions. In complexes 3-7, pentagonal bipyramidal [CuX] units are bridged by CN groups to give 1D [CuX(CN)] inorganic chains, which are charge-balanced by the surrounded alkylimidazolium cations. 2D inorganic [CuClI(CN)] layer in complex 8 is alternately packed with [VMIM] organic cations. In complex 9, left- and right-handed Cu-CN helical chains connect each other to give a 3D open framework, which are further entrapped by 1D zigzag Cu-CN chains and [PMIM] cations. Diverse unique Cu(I) atoms and cyanide or halide bridging groups in 10, 11, and 12 are extended into 3D anionic open frameworks with 1D channels, which are occupied by alkylimidazolium cations. For all hybrid halogeno(cyano)cuprate complexes, the extensively existing C-H···X or C-H···π hydrogen bonds help to stabilize the ultimate supramolecular packing structures. Notably, the distances between adjacent Cu(I) centers range from 2.420(2) to 2.989(2) Å in all polymeric frameworks, which indicate strong Cu···Cu interactions. Thanks to the cooperation of conjugate π electron cyanide systems with halide ions and/or Cu···Cu interactions, compounds 1-12 all demonstrate strong solid-state photoluminescence and semiconducting performance. Specially, hybrid halogeno(cyano)cuprates reported herein first exhibit excellent photocatalytic degradation of organic dye. To the best of our knowledge, fewer than 10 crystalline halogeno(cyano)cuprate compounds were obtained before this work, although different synthetic routes have been involved. Clearly, the discovery of this large hybrid material family under ionothermal conditions is important for the further development of novel functional halogeno(cyano) filled-shell d metal crystalline materials.

摘要

本工作开发了一种在离子液体中制备多功能卤代(氰基)铜酸盐材料的通用方法。在离子热条件下,基于烷基咪唑鎓的离子液体作为溶剂、电荷补偿剂、结构导向剂以及反应物,生成了12种新型杂化卤代(氰基)铜酸盐家族成员,其通式为[RRRIM][CuX(CN)](RRRIM = 烷基咪唑鎓阳离子,X = 卤化物阴离子)。X射线单晶衍射表明,各种无机卤代(氰基)铜酸盐组分从离散配合物(1和2)、一维(1D)链(3 - 7)、二维(2D)层(8)到三维(3D)开放框架(9 - 12)各不相同。1和2具有零维离散结构,包含三角形[CuX]阴离子。在配合物3 - 7中,五角双锥[CuX]单元由CN基团桥连形成1D [CuX(CN)]无机链,其电荷由周围的烷基咪唑鎓阳离子平衡。配合物8中的二维无机[CuClI(CN)]层与[VMIM]有机阳离子交替堆积。在配合物9中,左旋和右旋的Cu - CN螺旋链相互连接形成三维开放框架,该框架进一步被一维锯齿状Cu - CN链和[PMIM]阳离子包围。10、11和12中不同的独特Cu(I)原子以及氰化物或卤化物桥连基团扩展成具有一维通道的三维阴离子开放框架,这些通道被烷基咪唑鎓阳离子占据。对于所有杂化卤代(氰基)铜酸盐配合物,广泛存在的C - H···X或C - H···π氢键有助于稳定最终的超分子堆积结构。值得注意的是,在所有聚合物框架中,相邻Cu(I)中心之间的距离范围为2.420(2)至2.989(2) Å,这表明存在强的Cu···Cu相互作用。由于共轭π电子氰化物体系与卤离子和/或Cu···Cu相互作用的协同作用,化合物1 - 所有都表现出强的固态光致发光和半导体性能。特别地,本文报道的杂化卤代(氰基)铜酸盐首次表现出对有机染料的优异光催化降解性能。据我们所知,尽管涉及不同的合成路线,但在本工作之前获得的结晶卤代(氰基)铜酸盐化合物少于10种。显然,在离子热条件下发现这个大型杂化材料家族对于新型功能性卤代(氰基)填充壳层d金属晶体材料的进一步发展具有重要意义。

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