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

机译:Tris(联吡啶)金属(II)模板的3D碱-钌草酸盐配位框架的组合:减水过程中的晶体结构表征和光催化活性

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摘要

A series of 3D oxalate-bridged ruthenium-based coordination polymers with the formula of {[ZII(bpy)3][MIRu(C2O4)3]}n (ZII = Zn2+ (>1), Cu2+ (>3, >4), Ru2+ (>5, >6), Os2+ (>7, >8); MI = Li+, Na+; bpy = 2,2’-bipyridine) and {[ZnII(bpy)3](H2O)[LiRu(C2O4)3]}n (>2) 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 [ZII(bpy)3]2+ 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 >1–>8 can be tuned in a rational way by judicious choice of [ZII(bpy)3]2+ 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.
机译:一系列具有{{Z II (bpy)3] [M I Ru(C2O4)3]} n的3D草酸盐桥联钌基配位聚合物(Z II = Zn 2 + (> 1 ),Cu 2 + (> 3 >,> 4 ),Ru 2 + (> 5 ,> 6 ),Os 2 + (> 7 ,> 8 ); M I = Li + ,Na + ; bpy = 2,2'-联吡啶)和{[Zn II (bpy)3](H2O)[LiRu(C2O4)3]} n(> 2 )通过在水性介质中的自组装反应在室温下合成,具有单晶和粉末X射线衍射,元素分析,红外和漫反射UV-Vis光谱和热重分析的特征。所有化合物的晶体结构均包含srs型手性3D蜂窝状聚合物网,它们具有三角形阴离子笼,其中[Z II (bpy)3] 2 + 阳离子模板被选择性地嵌入。结构分析表明,阳离子客体的电子构型受到与阴离子骨架的静电相互作用的影响。此外,可以通过明智地选择[Z II (bpy)3]以合理的方式调整> 1 – > 8 的MLCT带隙值。 ] 2 + 位客人。 3D主客体聚合物体系结构可以用作自支撑的多相光催化剂,用于水的还原性裂解,在紫外光照射下对H2的析出表现出光催化活性。

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