Interconversion between Discrete and a Chain of Nanocages: Self-Assembly via a Solvent-Driven, Dimension-Augmentation Strategy
摘要:
Using a ligand bearing a bulky hydrophobic group, a "shish kabob" of nanocages, has been assembled through either a one-fell-swoop or a step-by-step procedure by varying the dielectric constant of the assembly mixture. A hydrophobic solvent breaks down the chain to discrete nanocages, while a hydrophilic solvent reverses the procedure. Although the shish kabob of nanocages has exactly the same chemical composition and even the same Archimedean-solid structure as those of its discrete analogue, its gas-adsorption capacity is remarkably improved because assembly of a chain exposes the internal surface of an individual cage. This dimension-augmentation strategy may have general implications in the preparation of porous materials.
([Co(TEPA)(TPT)2/3]·2DMF·H2O) and 2 ([Co(EPA)(TPT)]·1.5DMF·1.5H2O) show excellent luminescence properties. Meanwhile, as fluorescentsensors, complexes 1 and 2 exhibit selectivity and sensitivity for Fe3+ with the Ksv of 1.520 × 104 L/mol and 3.543 × 104 L/mol, which can rapidly detect nitroaromatic compounds in methanol and ethanol, especially for 2,4-NPH through fluorescence quenching with high quenching efficiency
摘要在设计两个含有炔基官能团的配体的前提下,成功合成了两种结构不同的Co(II)-MOF。配合物1([Co(TEPA)(TPT)2/3]·2DMF·H2O)和2([Co(EPA)(TPT)]·1.5DMF·1.5H2O)显示出优异的发光性能。同时,作为荧光传感器,配合物1和2对Fe3 +表现出选择性和敏感性,Ksv为1.520×104 L / mol和3.543×104 L / mol,可以快速检测甲醇和乙醇中的硝基芳香族化合物,尤其是对2,4 -NPH通过荧光猝灭具有很高的猝灭效率。特别是,配合物1和2相对于2,4-NPH的Ksv值可以达到1.627×105 L / mol和9.600×104 L / mol,这表明配合物1和2是识别和检测二甲双胍的良好候选者。 Fe3 +和硝基芳香族化合物。
(Bio)Functionalisation of Metal–Organic Polyhedra by Using Click Chemistry
Copper(I)-catalysed alkyne-azide cycloaddition click chemistry is a versatile post-synthetic tool to functionalize the surface chemistry of alkyne-functionalized cuboctahedral Metal–Organic Polyhedra (MOPs). This methodology enables quantitative functionalization of MOPs with a wide range of functional groups, including polymers, carboxylic and phosphonicacids and biomolecules.
Interconversion between Discrete and a Chain of Nanocages: Self-Assembly via a Solvent-Driven, Dimension-Augmentation Strategy
作者:Tian-Fu Liu、Ying-Pin Chen、Andrey A. Yakovenko、Hong-Cai Zhou
DOI:10.1021/ja306150x
日期:2012.10.24
Using a ligand bearing a bulky hydrophobic group, a "shish kabob" of nanocages, has been assembled through either a one-fell-swoop or a step-by-step procedure by varying the dielectric constant of the assembly mixture. A hydrophobic solvent breaks down the chain to discrete nanocages, while a hydrophilic solvent reverses the procedure. Although the shish kabob of nanocages has exactly the same chemical composition and even the same Archimedean-solid structure as those of its discrete analogue, its gas-adsorption capacity is remarkably improved because assembly of a chain exposes the internal surface of an individual cage. This dimension-augmentation strategy may have general implications in the preparation of porous materials.
Thermosensitive gating effect and selective gas adsorption in a porous coordination nanocage
作者:Dan Zhao、Daqiang Yuan、Rajamani Krishna、Jasper M. van Baten、Hong-Cai Zhou
DOI:10.1039/c0cc02771e
日期:——
A porous coordination nanocage functionalized with 24 triisopropylsilyl groups exhibits a remarkable thermosensitive gate opening phenomenon and demonstrates a molecular sieving effect at a certain temperature range, which can be used for gas separation purposes.