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三维碱式钌草酸配位框架的三联(联吡啶)金属(II)模板组装体:晶体结构、表征及水还原中的光催化活性

Tris(bipyridine)Metal(II)-Templated Assemblies of 3D Alkali-Ruthenium Oxalate Coordination Frameworks: Crystal Structures, Characterization and Photocatalytic Activity in Water Reduction.

作者信息

Dikhtiarenko Alla, Villanueva-Delgado Pedro, Valiente Rafael, García José R, Gimeno José

机构信息

Organic and Inorganic Chemistry Department, University of Oviedo-CINN, 33006 Oviedo, Spain.

Department of Chemistry and Biochemistry, University of Bern, 3012 Bern, Switzerland.

出版信息

Polymers (Basel). 2016 Feb 15;8(2):48. doi: 10.3390/polym8020048.

Abstract

A series of 3D oxalate-bridged ruthenium-based coordination polymers with the formula of {[Z(bpy)₃][MRu(C₂O₄)₃]} (Z = Zn (), Cu (, ), Ru (, ), Os (, ); M = Li⁺, Na⁺; bpy = 2,2'-bipyridine) and {Zn(bpy)₃[LiRu(C₂O₄)₃]} () has been synthesized at room temperature through a self-assembly reaction in aqueous media and characterized by single-crystal and powder X-ray diffraction, elemental analysis, infrared and diffuse reflectance UV⁻Vis spectroscopy and thermogravimetric analysis. The crystal structures of all compounds comprise chiral 3D honeycomb-like polymeric nets of the srs-type, which possess triangular anionic cages where [Z(bpy)₃] cationic templates are selectively embedded. Structural analysis reveals that the electronic configuration of the cationic guests is affected by electrostatic interaction with the anionic framework. Moreover, the MLCT bands gaps values for ⁻ can be tuned in a rational way by judicious choice of [Z(bpy)₃] guests. The 3D host-guest polymeric architectures can be used as self-supported heterogeneous photocatalysts for the reductive splitting of water, exhibiting photocatalytic activity for the evolution of H₂ under UV light irradiation.

摘要

一系列化学式为{[Z(bpy)₃][MRu(C₂O₄)₃]}(Z = Zn(),Cu(,),Ru(,),Os(,);M = Li⁺,Na⁺;bpy = 2,2'-联吡啶)和{Zn(bpy)₃[LiRu(C₂O₄)₃]}()的三维草酸桥连钌基配位聚合物已在室温下通过水介质中的自组装反应合成,并通过单晶和粉末X射线衍射、元素分析、红外和漫反射紫外可见光谱以及热重分析进行了表征。所有化合物的晶体结构均包含srs型手性三维蜂窝状聚合物网络,其中存在三角形阴离子笼,[Z(bpy)₃]阳离子模板选择性地嵌入其中。结构分析表明,阳离子客体的电子构型受与阴离子骨架的静电相互作用影响。此外,通过明智地选择[Z(bpy)₃]客体,可以合理调节⁻的MLCT带隙值。这种三维主客体聚合物结构可作为自支撑的多相光催化剂用于水的还原分解,在紫外光照射下对H₂的析出表现出光催化活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e633/6432594/6c97db8b88ef/polymers-08-00048-g001.jpg

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