RESUMO
The solvent-assisted linker exchange (SALE) method was used to produce amino-functionalized yttrium-based UiO-66 [NH2UiO-66(Y)], which is not obtainable via a direct synthetic method. Remarkably, SALE not only produced relatively highly porous NH2UiO-66(Y) from completely non-porous 3,3-bpdc-Y but also changed the network topology from 8-connected bcu in 3,3-bpdc-Y to 12-connected fcu in NH2UiO-66(Y). Based on our knowledge, this is one of the rare cases where SALE changes the whole network topology of the resulting metal-organic framework. NH2UiO-66(Y) also showed promising ability for selective detection of Cu2+ at a low concentration.
RESUMO
Herein we propose a new approach for deducing the topology of metal-organic frameworks (MOFs) assembled from organic ligands of low symmetry, which we call net-clipping. It is based on the construction of nets by rational deconstruction of edge-transitive nets comprising higher-connected molecular building blocks (MBBs). We have applied net-clipping to predict the topologies of MOFs containing zigzag ligands. To this end, we derived 2-connected (2-c) zigzag ligands from 4-c square-like MBBs by first splitting the 4-c nodes into two 3-c nodes and then clipping their two diagonally connecting groups. We demonstrate that, when this approach is applied to the 17 edge-transitive nets containing square-like 4-c MBBs, net-clipping leads to generation of 10 nets with different underlying topologies. Moreover, we report that literature and experimental research corroborate successful implementation of our approach. As proof-of-concept, we employed net-clipping to form three new MOFs built with zigzag ligands, each of which exhibits the deduced topology.
RESUMO
Owing to their high surface area, high concentration of active metal sites, and water stability, zirconium(VI)-based metal-organic frameworks (Zr-MOFs) have shown excellent activity in the hydrolysis of organophosphorus nerve agents (OPNs). In this regard, for the first time, two topologically different Zr-MOFs (Zr-fcu-tmuc and Zr-bcu-tmuc, constructed from the same organic and inorganic building blocks; fcu=face-centered cubic, bcu=body-centered cubic) have been rationally chosen to investigate the effect of network topology on the catalytic hydrolysis of the nerve agent simulant, dimethyl 4-nitrophenyl phosphate (DMNP). A remarkable enhancement in the hydrolysis rate of DMNP was observed with Zr-bcu-tmuc, reducing the half-life more than three-fold compared with Zr-fcu-tmuc. Greater accessibility of the active ZrVI sites in the 8-connected bcu net compared with the 12-connected fcu leads to a faster hydrolysis of DMNP on Zr-bcu-tmuc. Interestingly, the higher activity of Zr-bcu-tmuc was also confirmed by its higher fluorescence sensitivity towards DMNP (limit of detection (LOD)=0.557â µm) compared with Zr-fcu-tmuc (LOD=1.09â µm). The results show that controlling the desired topology of Zr-MOFs is a useful strategy for improving their performance in the detection and catalytic detoxification of OPNs.
RESUMO
Developing multifunctional materials from earth-abundant elements is urgently needed to satisfy the demand for sustainable energy. Herein, we demonstrate a facile approach for the preparation of a metal-organic framework (MOF)-derived Fe2O3/C, composited with N-doped reduced graphene oxide (MO-rGO). MO-rGO exhibits excellent bifunctional electrocatalytic activities toward the oxygen evolution reaction (ηj=10 = 273 mV) and the oxygen reduction reaction (half-wave potential = 0.77 V vs reversible hydrogen electrode) with a low ΔEOER-ORR of 0.88 V in alkaline solutions. A Zn-air battery based on the MO-rGO cathode displays a high specific energy of over 903 W h kgZn-1 (â¼290 mW h cm-2), an excellent power density of 148 mW cm-2, and an open-circuit voltage of 1.430 V, outperforming the benchmark Pt/C + RuO2 catalyst. We also hydrothermally synthesized a Ni-MOF that was partially transformed into a Ni-Co-layered double hydroxide (MOF-LDH). A MO-rGO||MOF-LDH alkaline battery exhibits a specific energy of 42.6 W h kgtotal mass-1 (106.5 µW h cm-2) and an outstanding specific power of 9.8 kW kgtotal mass-1 (24.5 mW cm-2). This work demonstrates the potential of MOFs and MOF-derived compounds for designing innovative multifunctional materials for catalysis, electrochemical energy storage, and beyond.
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A 3D, porous Zn(II)-based metal-organic framework {[Zn2(oba)2(4-bpmn)]·(DMF)1.5}n (TMU-21), (4-bpmn=N,N'-Bis-pyridin-4-ylmethylene-naphtalene-1,5-diamine, H2oba=4,4'-oxybis(benzoic acid)) with nano-rods morphology under ultrasonic irradiation at ambient temperature and atmospheric pressure was prepared and characterized by scanning electron microscopy. Sonication time and concentration of initial reagents effects on the size and morphology of nano-structured MOFs were studied. Also {[Zn2(oba)2(4-bpmn)] (TMU-21) and {[Zn2(oba)2(4-bpmb)] (TMU-6), 4-bpmb=N,N'-(1,4-phenylene)bis(1-(pyridin-4-yl)methanimine) were easily prepared by mechanochemical synthesis. Nanostructures of Zinc(II) oxide were obtained by calcination of these compounds and their de-solvated analogue as activated MOFs, at 550°C under air atmosphere. As a result of that, different Nanostructures of Zinc(II) oxide were obtained. The ZnO nanoparticles were characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and FT-IR spectroscopy.
RESUMO
Two novel Ru(II) complexes [(η6-p-cymene)RuCl(L2)]PF6 (R2) and [(η6-C6H6)RuCl(L2)]PF6 (R4), with ligand (E)-N-((6-bromopyridin-2-yl)methylene)-4-(methylthio)aniline (L2), were synthesized and characterized by elemental analysis, 1H NMR, 13C NMR and IR spectroscopy. Based on X-ray crystallography studies, complexes R2 and R4 have coordination environments with formulated (η6-p-cymene)Ru(N2Cl) and (η6-C6H6)Ru(N2Cl), respectively. The thermal stabilities of compounds R2 and R4 were studied by thermal gravimetric (TG) and differential scanning calorimetry (DSC). Thermal decomposition of these complexes was at 280°C and 260°C under air atmosphere respectively. The interaction of these complexes with calf thymus DNA (CT-DNA) was explored through electronic absorption spectra, fluorescence and redox behavior studies. The results showed that the complexes bind to CT-DNA with electrostatic interactions. Nanoparticles of RuO2 were prepared by calcination of R2 and R4. Also the role of the ultrasound waves on the characteristics of the RuO2 nanoparticles was studied. The nanoparticles were characterized by IR spectroscopy and X-ray diffraction (XRD). Also size and morphology of nanoparticles were studied by scanning electron microscopy (SEM).
RESUMO
Two new Hg(II) coordination polymers containing N,N'-Bis-pyridin-3-ylmethylene-naphtalene-1,5-diamine ligand were synthesized by conventional and sonochemical methods, characterized by spectroscopic techniques (FT-IR and elemental analysis), and their X-ray crystallographic structures were determined. The crystal packing and supramolecular features of these coordination polymers were studied using geometrical analysis and Hirshfeld surface analysis. The crystal structure analysis revealed that Hâ¯H contacts, C-Hâ¯π and C-Hâ¯X (X = Cl for 1 and X = Br for 2) hydrogen bonding interactions are strong enough to govern the supramolecular architecture. The BFDH analysis helps us to compare the predicted morphology to that obtained under ultrasonication. This study may provide further insight into discovering the role of weak intermolecular interactions in the context of nano-supramolecular assembly.