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Due to their hazard to biological systems, it is urgent to develop materials that can rapidly and sensitively detect the concentration of H2PO4− and OCN− ions. In this work, a new CdII-based luminescent metal–organic framework with the formula [Cd(BTDB)(2,6-BBIP)]n (JXUST-47, H2BTDB = (benzo[c][1,2,5]thiadiazole-4,7-diyl)dibenzoic acid, 2,6-BBIP = 2,6-bis(benzimidazol-1-yl)pyridine) and sql topology was successfully synthesized using a mixed-ligand strategy. JXUST-47 shows good chemical and thermal stability. It also exhibits weak quenching and fluorescence blue shift for H2PO4− and red shift for OCN−, with the detection limits of 0.106 and 0.128 mM, respectively. In addition, considering the demand for H2PO4− and OCN− ion detection, by combining this with the functions of a smartphone, the chroma of photographs have been used to realize the consecutive visual detection of the concentration of these ions. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) are a novel class of hybrid porous multi-functional materials consisting of metal ions/clusters and organic ligands. MOFs have exclusive benefits due to their tunable structure and diverse properties. Luminescent MOFs (LMOFs) exhibit both porosity and light emission. They display abundant host and guest responses, making them conducive to sensing. Currently, LMOF sensing research is gaining more depth, with attention given to their device and practical applications. This work reviews recent advancements and device applications of LMOFs as chemical sensors toward ions, volatile organic compounds, biomolecules, and environmental toxins. Furthermore, the detection mechanism and the correlation between material properties and structure are elaborated. This analysis serves as a valuable reference for the preparation and efficient application of targeted LMOFs. [ABSTRACT FROM AUTHOR]

Revealing the stimuli-responsive mechanism is the key to the accurate design of stimuli-responsive luminescent materials. We report herein the multistimuli-responsive multicolor solid-state luminescence of a new dicopper(I) complex [{Cu(bpmtzH)}2(μ-dppa)2](ClO4)2 (1), and the multistimuli-responsive mechanism is clarified by investigating its four different solvated compounds 1·2CH3COCH3·2H2O, 1·2DMSO·2H2O, 1·4CH3OH, and 1·4CH2Cl2. It is shown that luminescence mechanochromism is associated with the breakage of the hydrogen bonds of bmptzH-NH with counter-ions such as ClO4− induced by grinding, while luminescence vapochromism is attributable to the breaking and forming of hydrogen bonds of dppa-NH with solvents, such as acetone, dimethylsulfoxide, and methanol, caused by heating and vapor fuming. In addition, those results might provide new insights into the design and synthesis of multistimuli-responsive multicolor luminescent materials by using various structure-sensitive functional groups, such as distinct N–H ones, to construct switchable hydrogen bonds. [ABSTRACT FROM AUTHOR]

Due to their hazard to biological systems, it is urgent to develop materials that can rapidly and sensitively detect the concentration of H2PO4− and OCN− ions. In this work, a new CdII-based luminescent metal–organic framework with the formula [Cd(BTDB)(2,6-BBIP)]n (JXUST-47, H2BTDB = (benzo[c][1,2,5]thiadiazole-4,7-diyl)dibenzoic acid, 2,6-BBIP = 2,6-bis(benzimidazol-1-yl)pyridine) and sql topology was successfully synthesized using a mixed-ligand strategy. JXUST-47 shows good chemical and thermal stability. It also exhibits weak quenching and fluorescence blue shift for H2PO4− and red shift for OCN−, with the detection limits of 0.106 and 0.128 mM, respectively. In addition, considering the demand for H2PO4− and OCN− ion detection, by combining this with the functions of a smartphone, the chroma of photographs have been used to realize the consecutive visual detection of the concentration of these ions. [ABSTRACT FROM AUTHOR]

Due to their hazard to biological systems, it is urgent to develop materials that can rapidly and sensitively detect the concentration of H 2 PO 4 - and OCN - ions. In this work, a new Cd II -based luminescent metal-organic framework with the formula [Cd(BTDB)(2,6-BBIP)] n (JXUST-47, H 2 BTDB = (benzo[ c ][1,2,5]thiadiazole-4,7-diyl)dibenzoic acid, 2,6-BBIP = 2,6-bis(benzimidazol-1-yl)pyridine) and sql topology was successfully synthesized using a mixed-ligand strategy. JXUST-47 shows good chemical and thermal stability. It also exhibits weak quenching and fluorescence blue shift for H 2 PO 4 - and red shift for OCN - , with the detection limits of 0.106 and 0.128 mM, respectively. In addition, considering the demand for H 2 PO 4 - and OCN - ion detection, by combining this with the functions of a smartphone, the chroma of photographs have been used to realize the consecutive visual detection of the concentration of these ions.

Metal-organic frameworks (MOFs) are a novel class of hybrid porous multi-functional materials consisting of metal ions/clusters and organic ligands. MOFs have exclusive benefits due to their tunable structure and diverse properties. Luminescent MOFs (LMOFs) exhibit both porosity and light emission. They display abundant host and guest responses, making them conducive to sensing. Currently, LMOF sensing research is gaining more depth, with attention given to their device and practical applications. This work reviews recent advancements and device applications of LMOFs as chemical sensors toward ions, volatile organic compounds, biomolecules, and environmental toxins. Furthermore, the detection mechanism and the correlation between material properties and structure are elaborated. This analysis serves as a valuable reference for the preparation and efficient application of targeted LMOFs.