首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Di-pyridyl organic cation directed hybrid cuprous halogenides: syntheses, crystal structures and photochromism and photocatalysis
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Di-pyridyl organic cation directed hybrid cuprous halogenides: syntheses, crystal structures and photochromism and photocatalysis

机译:取向杂交亚铜卤化物的二吡啶基有机阳离子:合成,晶体结构和光学变色和光催化

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摘要

By using 1,3-di(4-pyridyl)-propane (dpp) as templates or structure-directing agents (SDAs), a series of hybrid cuprous halogenides, namely, [H(2)dpp](2)[Cu4I8]center dot H2O (1), [H(2)dpp][Cu2I4] (2), [H(2)dpp](2)Cu11I15 (3) and [H(2)dpp](2)Cu11Br15 (4), have been solvothermally prepared and structurally characterized. Despite the similar chemical compositions, compound 1 features a zero-dimensional (0D) [Cu4I8](4-) unit and compound 2 contains one-dimensional (1D) [Cu2I4](2-) chains, which are both separated by [H(2)dpp](2+) organic cations. Compounds 3-4 contain two-dimensional (2D) microporous [Cu11X15](4-) (X = I, Br) layers composed of the [Cu9X17] unit interconnected by [CuX4] tetrahedra. The UV-vis diffuse-reflectance measurements reveal that the compounds 3-4 exhibit semiconducting behaviors with narrow band gaps of 1.48 and 2.21 eV, respectively, which lead to efficient photocatalytic degradation activities over an organic pollutant under visible light irradiation. The possible photocatalytic mechanism is also proposed based on experimental and theoretical studies. Furthermore, compound 1 shows interesting photochromism behavior maybe owing to the photo-induced intermolecular charge transfer.
机译:通过使用1,3-DI(4-吡啶基) - 丙烷(DPP)作为模板或结构引导剂(SDAS),一系列杂化亚杂物卤化物,即[H(2)DPP](2)[CU4I8]中心点H 2 O(1),[H(2)DPP] [Cu 2 I4](2),[H(2)DPP](2)Cu11i15(3)和[H(2)DPP](2)CU11BR15(4) ,已经在结构上并在结构上表现出来。尽管具有类似的化学组合物,但化合物1具有零维(0d)[Cu4i8](4-)单元,化合物2含有一维(1D)[Cu 2 I4](2-)链,其均分开[H. (2)DPP](2+)有机阳离子。化合物3-4含有由互联的[Cu9X17]单元组成的二维(2D)微孔[Cu11x15](4-)(X = I,Br)层。 UV-Vis弥射反射率测量表明,化合物3-4分别表现出具有1.48和2.21eV的窄带间隙的半导体行为,这导致在可见光照射下的有机污染物上有效的光催化降解活性。还基于实验和理论研究提出了可能的光催化机制。此外,化合物1显示出可感兴趣的光学变色行为,可能由于光诱导的分子间电荷转移。

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