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The association of some small molecules such as benzene and phthalimide with non-amphiphilic homopolymeric low-entropy chains such as PVAc, PVA, PVP, and PNIPAM has been realized by reversible addition–fragmentation chain transfer reaction (RAFT) method. The as-prepared PT-PVA, PT-PVAc, PT-PVP, and PT-PNIPAM can serve as new building blocks and show the capability in concentration-dependent multidimensional self-assembly from vesicles to nanotubes, nanoribbons, and three-dimensional porous net-sheet structures. The introduction of low-entropy chains enables small molecules to aggregate into the J-type formation, which confers small molecules with the fluorescence-color-tunable ability. Incidentally, due to the essence of loosely stacking of J-type aggregates, reversible disassembly of the systems has also ensued. In particular, biocompatible PT-PVA shows excellent cell-labeling and sustained-drug-release abilities. This system promises potential applications in preparing sophisticated nanostructures and designing new sustained-drug-release systems from simple small molecules. [ABSTRACT FROM AUTHOR]

By means of a mixed-ligand strategy, a novel bi-functional metal–organic framework, [H2N(CH3)2]·Zn(NDC)(atz)·H2O (NDC = 2,6-naphthalenedicarboxylic acid, Hatz = 1H-tetrazol-5-amine), was synthesized, which displays a three-dimensional two-fold interpenetrated framework. Owing to the introduction of two different functional organic ligands, this complex exhibits bi-functional properties, i.e., selective gas adsorption of CO2 over CH4 and fluorescence sensing response for nitrobenzene. [ABSTRACT FROM AUTHOR]

A 3D metal–organic framework, [NH2(CH3)2]2[Cd17(L)12(μ3-H2O)4(DMF)2(H2O)2]·solvent (1), has been constructed with a π-electron rich aromatic ligand 2,4,6-tris[1-(3-carboxylphenoxy)ylmethyl]mesitylene (H3L) and d10 configuration metal ion Cd2+ under solvothermal conditions. The crystal structure reveals that complex 1 consists of hexanuclear and trinuclear cadmium building units, which are further bridged by the multicarboxylate ligands to give a (3, 6, 12)-connected topological net. This complex exhibits strong ligand originated photoluminescence emission, which is selectively sensitive to electron-deficient nitroaromatic explosives (nitrobenzene, 4-nitrotoluene, 1,4-dinitrobenzene, 1,3-dinitrobenzene and 2,4-dinitrotoluene). This property makes complex 1 a potential fluorescence sensor for these chemicals. [ABSTRACT FROM AUTHOR]

By means of a mixed-ligand strategy, a novel bi-functional metal-organic framework, [H 2 N(CH 3 ) 2 ]·Zn(NDC)(atz)·H 2 O (NDC = 2,6-naphthalenedicarboxylic acid, Hatz = 1H-tetrazol-5-amine), was synthesized, which displays a three-dimensional two-fold interpenetrated framework. Owing to the introduction of two different functional organic ligands, this complex exhibits bi-functional properties, i.e., selective gas adsorption of CO 2 over CH 4 and fluorescence sensing response for nitrobenzene.