RESUMEN
A mixed-ligand strategy has been used to construct stable luminescent coordination polymers (CPs). An ultra-stable Zn(ii) coordination polymer, [Zn(H3tpb)(Hbtc)]n (1) was hydrothermally synthesized by employing a new tripodal pyrazole ligand H3tpb and a classical carboxylic ligand H3btc (H3tpb = 1,3,5-tris(pyrazolyl)benzene, H3btc = 1,3,5-benzenetricarboxylic acid). Complex 1 exhibits a 2D sql network. Importantly, 1 not only possesses excellent thermal stability but also shows superior chemical stability in terms of water resistance, acid/base aqueous solutions tolerance (pH = 2-12), and organic solvents resistance. This excellent structural stability was further illustrated from the perspective of thermal decomposition kinetics. The luminescence properties were investigated, showing that complex 1 displays high sensitivity and selectivity for detecting Fe3+ and Cr2O72- ions in aqueous solutions via luminescence quenching effects.
RESUMEN
A 3D lanthanide coordination polymer {[La(SIP)(H2O)3]·H2O}n (La-MOF) was synthesized successfully by the solvothermal reaction of La(NO3)3·6H2O and 5-sulfoisophthalic acid monosodium salt (NaH2SIP). In particular, two oxygen atoms of sulfate participate in the coordination, which is unusual in all the complexes. La-MOF was characterized by single-crystal X-ray diffraction, IR spectroscopy, powder X-ray diffraction, thermal-gravimetric analysis, and X-ray photoelectron spectroscopy. La-MOF shows excellent water stability and chemical stability in a broad pH range from 2 to 13. Moreover, the fluorescence and sensing properties of La-MOF were invsetigated in detail via its titration and cycling processes, revealing its highly efficient and selective quenching responses and good recyclability for the detection of Fe3+, Cr2O72- and CrO42- ions. In addition, La-MOF possesses an outstanding specific capacitance of 213 F g-1 at 0.5 A g-1. It still retains 92% of the original capacitance after 2000 cycles, exhibiting remarkable long-term cycling stability and reversibility; therefore, the electrode material based on La-MOF is a competitive and promising candidate for application in supercapacitors.
RESUMEN
An interpenetrated indium pyridylcarboxylate framework, [NH2(CH3)2][In(L)2]·2.5DMF·5H2O (1), has been synthesized by employing a pyridylcarboxylate ligand, 4-(3-carboxylphenyl)picolinic acid (H2L), and an In3+ ion, with both chemical stability and framework flexibility. The desolvated 1 exhibits an uncommon breathing sorption behavior and shows highly selective adsorption for C2H2, C2H4, and CO2 over CH4. Furthermore, 1 shows rapid and higher adsorption efficiency for methylene blue and neutral red in aqueous solution.
RESUMEN
By employing a pyridyl-decorated dicarboxylic acid ligand, 3-(2',5'-dicarboxylphenyl)pyridine acid (H2dcpy), a three-dimensional In3+-based metal-organic framework, H3O[In3(dcpy)4(OH)2]·3DMF·4H2O (1), with a good chemical stability toward acid and base has been synthesized. The compound 1 shows an uncommon (3,8)-connected tfz-d; UO3 topological net based on linear In3(COO)4(OH)2 clusters and also contains one-dimensional open channels. Particularly, 1 contains two types of dcpy2- linkers, in which the pyridyl group in one participates in coordination with the In3+ ion, whereas that in the other is uncoordinated but hangs in the inner sides of the channels as functionalized sites. Gas adsorption experiments demonstrate that 1 is able to selectively adsorb C2H2, C2H4, and CO2 over CH4. Simultaneously, 1 shows a highly selective and sensitive fluorescence detection toward Fe3+ ion in water with good recyclability.