A new mixed lanthanide metal-organic framework thermometer Tb0.9Eu0.1PIA with the significantly high sensitivity of 3.53% per K has been realized by making use of an organic ligand, 5-(pyridin-4-yl)isophthalate, with higher triplet state energy.

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A microporous MOF [Zn(4)(OH)(2)(1,2,4-BTC)(2)] (1,2,4-BTC = Benzene-1,2,4-tricarboxylate) with two immobilized open metal Zn(2+) sites was obtained by solvothermal reaction, which exhibits highly selective guest sorption and sensing of nitrobenzene.

A new microporous metal-organic framework, Cu2(PDDI) (ZJU-5; H4PDDI = 5,5'-(pyridine-2,5-diyl)diisophthalic acid), was solvothermally synthesized and structurally characterized. With open metal sites, Lewis basic pyridyl sites and suitable pore space, the acetylene uptake in ZJU-5a reaches the highest value of 290 cm(3) g(-1) at 273 K and 1 bar. Furthermore, ZJU-5a exhibits high absolute methane storage of 190 cm(3) (STP) cm(-3) at 35 bar and 224 cm(3) (STP) cm(-3) at 60 bar at room temperature.

A nanoscale MOF material NMOF 1 with controllable morphologies is realized whose morphology control has been simulated based on the BFDH method. The targeted NMOF 1 exhibits highly sensitive, selective and instant "turn-on" sensing of bacterial endospores.

An important result of research on mixed-lanthanide metal-organic frameworks (M'LnMOFs) is the realization of highly sensitive ratiometric luminescent thermometers. Here, we report the design and synthesis of the new M'LnMOF Tb0.80Eu0.20BPDA with high relative sensitivity in the physiological temperature regime (298-318 K). The emission intensity and luminescence lifetime were investigated and compared to those of existing materials. It was found that the temperature-dependent luminescence properties of Tb0.80Eu0.20BPDA are strongly associated with the distribution of the energy levels of the ligand. Such a property can be useful in the design of highly sensitive M'LnMOF thermometers.

Two new chiral two-dimensional coordination networks, ZnL2(H2O)2 (1) and CdL2(H2O)2 (2) [L = 1,2,2-trimethyl-3-(pyridin-4-ylcarbamoyl)cyclopentanecarboxylic acid], have been synthesized and structurally characterized by single X-ray structure analysis, featuring very unusual interwoven (4,4) square grids of double helices. The frameworks exhibit high thermal stability as confirmed by thermogravimetric analysis and powder X-ray diffraction studies. The unique chiral networks attributed to the chiral organic linker have led to their nonlinear optical properties.

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