Counterion‐Directed Assembly of Praseodymium(III) Compounds based on the Flexible Ligand 5‐Aminotetrazole‐1‐propionic Acid (Hatzp)

Different kinds of counterions (such as NO₃^–, ClO₄^–, and Cl^–) play a special role in controlling the framework of coordination compounds. Using this strategy, 5‐aminotetrazole‐1‐propionic acid (Hatzp) was selected to react with praseodymium(III) nitrate or perchlorate in the same solvent system, producing two different coordination compounds, [Pr₂(atzp)₄(H₂O)₈] · 2NO₃ · 2H₂O ( 1 ) and [Pr₂(atzp)₆(H₂O)₂] · H₂O ( 2 ). These compounds were structurally characterized by elemental analysis, IR spectroscopy, and single‐crystal X‐ray diffraction. X‐ray diffraction analysis revealed that compound 1 displays a dinuclear structure, whereas 2 shows a one dimensional zigzag chain framework. Furthermore, the luminescence properties of compounds 1 and 2 were investigated at room temperature in the solid state.     

A fourfold interpenetrating cadmium(II) metal–organic framework based on 2,4,6‐tris(pyridin‐4‐yl)‐1,3,5‐triazine with reversible photochromic properties

2,4,6‐Tris(pyridin‐4‐yl)‐1,3,5‐triazine (tpt), as an organic molecule with an electron‐deficient nature, has attracted considerable interest because of its photoinduced electron transfer from neutral organic molecules to form stable anionic radicals. This makes it an excellent candidate as an organic linker in the construction of photochromic complexes. Such a photochromic three‐dimensional (3D) metal–organic framework (MOF) has been prepared using this ligand. Crystallization of tpt with Cd(NO₃)₂·4H₂O in an N,N‐dimethylacetamide–methanol mixed‐solvent system under solvothermal conditions afforded the 3D MOF poly[[bis(nitrato‐κ²O,O′)cadmium(II)]‐μ₃‐2,4,6‐tris(pyridin‐4‐yl)‐1,3,5‐triazine‐κ³N²:N⁴:N⁶], [Cd(NO₃)₂(C₁₈H₁₂N₆)]_n, which was characterized by IR spectroscopy, elemental analysis, thermogravimetric analysis and single‐crystal X‐ray diffraction. The X‐ray diffraction crystal structure analysis reveals that the asymmetric unit contains one independent Cd^II cation, one tpt ligand and two coordinated NO₃^? anions. The Cd^II cations are connected by tpt ligands to generate a 3D framework. The single framework leaves voids that are filled by mutual interpenetration of three independent equivalent frameworks in a fourfold interpenetrating architecture. The compound shows a good thermal stability and exhibits a reversible photochromic behaviour, which may originate from the photoinduced electron‐transfer generation of radicals in the tpt ligand.     

A Three‐dimensional DyIII‐based Metal‐organic Framework: Smart Drug Carrier and Anti‐lung Cancer Activity

A 3D lanthanide metal‐organic framework (MOF) with the formula [Dy₂(L)₂(H₂O)₂]_n ( 1 ) (H₃L = biphenyl‐3,4′,5‐tricarboxylic acid) was synthesized under solvothermal conditions and structurally characterized by elemental analysis, powder X‐ray diffraction analysis, infrared spectroscopy, and single‐crystal X‐ray diffraction analysis. Compound 1 features a 3D porous framework based on 1D rod‐shaped Dy^III‐carboxylate chains. The efficient encapsulation and controllable release of an anticancer drug (5‐Fu) make it a promising drug delivery host. Furthermore, the GCMC simulation was used to probe the drug‐framework interaction at the atomic lever. The in vitro anti‐lung cancer activity of 1 and 5‐Fu loaded 1a were also evaluated using MTT assay.     

A Co‐MOF with a (4,4)‐connected binodal two‐dimensional topology: synthesis,structure and photocatalytic properties

The Co‐MOF poly[[diaqua{μ₄‐1,1,2,2‐tetrakis[4‐(1H‐1,2,4‐triazol‐1‐yl)phenyl]ethylene‐κ⁴N:N′:N′′:N′′′}cobalt(II)] benzene‐1,4‐dicarboxylic acid benzene‐1,4‐dicarboxylate], {[Co(C₃₄H₂₄N₁₂)(H₂O)₂](C₈H₄O₄)·C₈H₆O₄}_n or {[Co(ttpe)(H₂O)₂](bdc)·(1,4‐H₂bdc)}_n, (I), was synthesized by the hydrothermal method using 1,1,2,2‐tetrakis[4‐(1H‐1,2,4‐triazol‐1‐yl)phenyl]ethylene (ttpe), benzene‐1,4‐dicarboxylic acid (1,4‐H₂bdc) and Co(NO₃)₂·6H₂O, and characterized by single‐crystal X‐ray diffraction, IR spectroscopy, powder X‐ray diffraction (PXRD), luminescence, optical band gap and valence band X‐ray photoelectron spectroscopy (VB XPS). Co‐MOF (I) shows a (4,4)‐connected binodal two‐dimensional topology with a point symbol of {4⁴·6²}{4⁴·6²}. The two‐dimensional networks capture free neutral 1,4‐H₂bdc molecules and bdc^2? anions, and construct a three‐dimensional supramolecular architecture via hydrogen‐bond interactions. MOF (I) is a good photocatalyst for the degradation of methylene blue and rhodamine B under visible‐light irradiation and can be reused at least five times.     

Selective Sensing of Fe3+ and Al3+ Ions and Detection of 2,4,6‐Trinitrophenol by a Water‐Stable Terbium‐Based Metal–Organic Framework

A water‐stable luminescent terbium‐based metal–organic framework (MOF), {[Tb(L₁)_1.5(H₂O)] ? 3 H₂O}_n (Tb‐MOF), with rod‐shaped secondary building units (SBUs) and honeycomb‐type tubular channels has been synthesized and structurally characterized by single‐crystal X‐ray diffraction. The high green emission intensity and the microporous nature of the Tb‐MOF indicate that it can potentially be used as a luminescent sensor. In this work, we show that Tb‐MOF can selectively sense Fe³⁺ and Al³⁺ ions from mixed metal ions in water through different detection mechanisms. In addition, it also exhibits high sensitivity for 2,4,6‐trinitrophenol (TNP) in the presence of other nitro aromatic compounds in aqueous solution by luminescence quenching experiments.     

A Stimuli‐Responsive Zirconium Metal–Organic Framework Based on Supermolecular Design

A flexible, yet very stable metal–organic framework (DUT‐98, Zr₆O₄(OH)₄(CPCDC)₄(H₂O)₄, CPCDC=9‐(4‐carboxyphenyl)‐9H ‐carbazole‐3,6‐dicarboxylate) was synthesized using a rational supermolecular building block approach based on molecular modelling of metal–organic chains and subsequent virtual interlinking into a 3D MOF. Structural characterization via synchrotron single‐crystal X‐ray diffraction (SCXRD) revealed the one‐dimensional pore architecture of DUT‐98, envisioned in silico. After supercritical solvent extraction, distinctive responses towards various gases stimulated reversible structural transformations, as detected using coupled synchrotron diffraction and physisorption techniques. DUT‐98 shows a surprisingly low water uptake but a high selectivity for pore opening towards specific gases and vapors (N₂, CO₂, n ‐butane, alcohols) at characteristic pressure resulting in multiple steps in the adsorption isotherm and hysteretic behavior upon desorption.     

A novel alkaline earth strontium(II) coordination polymer: poly[hexaaquatetrakis(μ5‐pyridine‐2,6‐dicarboxylato)bis(μ4‐pyridine‐2,6‐dicarboxylato)(μ7‐sulfato)heptastrontium(II)]

The title compound, [Sr₇(C₇H₃NO₄)₆(SO₄)(H₂O)₆]_n, has been synthesized by an ionothermal method using the ionic liquid 1‐ethyl‐3‐methylimidazolium ([Emim]Br) as solvent, and characterized by elemental analysis, energy‐dispersive X‐ray spectroscopy, IR and single‐crystal X‐ray diffraction. The structure of the compound can be viewed as a three‐dimensional coordination polymer composed of Sr²⁺ cations, pyridine‐2,6‐dicarboxylate anions, sulfate anions and water molecules. The compound not only exhibits a three‐dimensional structure with a unique coordination mode of the sulfate anion, but also features the first example of a heptanuclear strontium(II) coordination polymer. The structure is further stabilized by O—H...O hydrogen bonds and π–π stacking interactions.     

A Water‐Stable Uranyl Organic Framework as a Highly Selective and Sensitive Bifunctional Luminescent Probe for Fe3+ and Tetracycline Hydrochloride

A new coordination polymer (H₂bpy)_0.5?[(UO₂)_1.5(ipa)₂(H₂O)] ( 1 ) (H₂ipa=isophthalic acid, bpy=4,4′‐bipyridine) was synthesized by hydrothermal condition. It was characterized by IR spectroscopy, elemental analysis, TG‐DTA analysis, and powder X‐ray diffraction. Analysis of single‐crystal X‐ray diffraction results showed that the title compound exhibited a double chain bridged by the different uranyl ions and ipa^2? ligands. Through the hydrogen bond interactions and π???π stacking interactions, the double chains were assembled into the three‐dimensional supramolecular framework. Furthermore, the compound can be used as a promising bifunctional luminescence sensor for detecting and identifying Fe³⁺ and tetracycline hydrochloride antibiotic molecules with high selectivity and sensitivity in aqueous solutions. Moreover, the luminescent sensing mechanisms for different analytes were proposed. Moreover, the electronic properties of title compound were explored by density functional theory (DFT) calculations. The sensor system has been successfully applied for the detection of Fe³⁺ and tetracycline hydrochloride with high recovery percentages and low relative standard deviation in real river water samples.     

Tetrazine Chromophore‐Based Metal–Organic Frameworks with Unusual Configurations: Synthetic,Structural, Theoretical,Fluorescent, and Nonlinear Optical Studies

Three unusual three‐dimensional (3D) tetrazine chromophore‐based metal–organic frameworks (MOFs) {(Et₄N)[WS₄Cu₃(CN)₂(4,4′‐pytz)_0.5]}_n ( 1 ), {[MoS₄Cu₄(CN)₂(4,4′‐pytz)₂] ? CH₂Cl₂}_n ( 2 ), and {[WS₄Cu₃(4,4′‐pytz)₃] ? [N(CN)₂]}_n ( 3 ; 4,4′‐pytz=3,6‐bis(4‐pyridyl)tetrazine) have been synthesized and characterized by using FTIR and UV/Vis spectroscopy, elemental analysis, powder X‐ray diffraction, gel permeation chromatography, steady‐state fluorescence, and thermogravimetric analysis; their identities were confirmed by single‐crystal X‐ray diffraction studies. MOF 1 possesses the first five‐connected M/S/Cu (M=Mo, W) framework with an unusual 3D (4⁴?6⁶) topology constructed from T‐shaped [WS₄Cu₃]⁺ clusters as nodes and single CN^?/4,4′‐pytz bridges as linkers. MOF 2 features a novel 3D MOF structure with (4²⁰?6⁸) topology, in which the bridging 4,4′‐pytz ligands exhibit unique distorted arch structures. MOF 3 displays the first 3D MOF structure based on flywheel‐shaped [WS₄Cu₃]⁺ clusters with a non‐interpenetrating honeycomb‐like framework and a heavily distorted “ACS” topology. Steady‐state fluorescence studies of 1 – 3 reveal significant fluorescence emissions. The nonlinear optical (NLO) properties of 1 – 3 were investigated by using a Z‐scan technique with 5 ns pulses at λ=532 nm. The Z‐scan experimental results show that the π‐delocalizable tetrazine‐based 4,4′‐pytz ligands contribute to the strong third‐order NLO properties exhibited by 1 – 3 . Time‐dependent density functional theory studies afforded insight into the electronic transitions and spectral characterization of these functionalized NLO molecular materials.     

A novel dinuclear bismuth(III) coordination compound: bis(μ‐pyridine‐2,6‐dicarboxylato)‐κ4O2,N,O6:O6′;κ4O2:O2′,N,O6‐bis[(azido‐κN)(1,10‐phenanthroline‐κ2N,N′)bismuth(III)] tetrahydrate

A novel dinuclear bismuth(III) coordination compound, [Bi₂(C₇H₃NO₄)₂(N₃)₂(C₁₂H₈N₂)₂]·4H₂O, has been synthesized by an ionothermal method and characterized by elemental analysis, energy‐dispersive X‐ray spectroscopy, IR, X‐ray photoelectron spectroscopy and single‐crystal X‐ray diffraction. The molecular structure consists of one centrosymmetric dinuclear neutral fragment and four water molecules. Within the dinuclear fragment, each Bi^III centre is seven‐coordinated by three O atoms and four N atoms. The coordination geometry of each Bi^III atom is distorted pentagonal–bipyramidal (BiO₃N₄), with one azide N atom and one bridging carboxylate O atom located in axial positions. The carboxylate O atoms and water molecules are assembled via O—H...O hydrogen bonds, resulting in the formation of a three‐dimensional supramolecular structure. Two types of π–π stacking interactions are found, with centroid‐to‐centroid distances of 3.461 (4) and 3.641 (4) Å.     

A CdII‐Based Metal‐Organic Framework with pcu Topology as Turn‐On Fluorescent Sensor for Al3+

A new metal‐organic framework (MOF) {[Cd₂(bbib)₂(ndc)₂]?2DMF}_n ( JXUST‐1 ) (bbib=1,3‐bis(benzimidazolyl)benzene, H₂ndc=1,4‐naphthalenedicarboxylic acid, DMF=N,N‐dimethylformamide) has been solvothermally synthesized and characterized by single‐crystal X‐ray diffraction, PXRD, TGA, IR and elemental analysis. JXUST‐1 exhibits a three‐dimensional 6‐connected pcu topology with a Schläfli symbol {4¹².6³} constructed by [Cd₂(CO₂)₃] secondary building units. Fluorescence studies show that this MOF can sensitively and selectively recognize Al³⁺ via a fluorescence enhancement effect, and the detection limit is 0.048 ppm. Furthermore, JXUST‐1 displays relatively good thermal and chemical stabilities as well as reusability. All these results suggest JXUST‐1 to be a highly selective and recyclable luminescent sensing material for the detection of Al³⁺.     

A Novel Electrochemical Sensor Based on Copper‐based Metal‐Organic Framework for the Determination of Dopamine

A glassy carbon electrode (GCE) modified with a copper‐based metal‐organic framework (MOF) [HKUST‐1, HKUST‐1 = Cu₃(BTC)₂ (BTC = 1,3,5‐benzenetricarboxylicacid)] was developed as a highly sensitive and simple electrochemical sensor for the determination of dopamine (DA). The MOF was prepared by a hydrothermal process, and the morphology and crystal phase of the MOF were characterized by scanning electron microscopy (SEM) and X‐ray diffraction (XRD), respectively. Meanwhile, the electrochemical performance was investigated using cyclic voltammetry (CV), differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS). Under optimized conditions, the modified electrode showed excellent electrocatalytic activity and high selectivity toward DA. The linear response range was from 5.0 × 10⁻⁷ to 1.0 × 10⁻⁴ M and the detection limit was as low as 1.5 × 10⁻⁷ M. Moreover, the electrochemical sensor was used to detect DA in real samples with excellent results. MOF‐based sensors hold great promise for routine sensing applications in the field of electrochemical sensing.     

Efficient and recyclable novel Ni‐based metal–organic framework nanostructure as catalyst for the cascade reaction of alcohol oxidation–Knoevenagel condensation

A novel Ni‐based metal–organic framework (Ni‐MOF) with a Schiff base ligand as an organic linker, Ni₃(bdda)₂(OAc)₂?6H₂O (H₂bdda = 4,4′‐[benzene‐1,4‐diylbis(methylylidenenitrilo)]dibenzoic acid), was synthesized and characterized using powder X‐ray powder diffraction, thermogravimetric analysis, Brunauer–Emmett–Teller measurements, inductively coupled plasma atomic emission spectroscopy, transmission electron microscopy, elemental analysis and Fourier transform infrared spectroscopy. The synthesized Ni‐MOF exhibited a high catalytic activity in benzyl alcohol oxidation using tert‐butyl hydroperoxide under solvent‐free conditions. Also, the efficiency of the catalyst was investigated in the cascade reaction of oxidation–Knoevanagel condensation under mild conditions. The Ni‐MOF catalyst could be recovered and reused four times without significant reduction in its catalytic activity.     

Two new NiII and ZnII metal–organic frameworks of glutarate and 1,4‐bis[(2‐methyl‐1H‐imidazol‐1‐yl)methyl]benzene ligands: syntheses,structures and luminescence sensing properties

Two new metal–organic frameworks (MOFs), namely, three‐dimensional poly[diaquabis{μ₂‐1,4‐bis[(2‐methyl‐1H‐imidazol‐1‐yl)methyl]benzene}bis(μ₂‐glutarato)dinickel(II)] monohydrate], {[Ni₂(C₅H₆O₄)₂(C₁₆H₁₈N₄)₂(H₂O)₂]·H₂O}_n or {[Ni₂(Glu)₂(1,4‐mbix)₂(H₂O)₂]·H₂O}_n, ( I ), and two‐dimensional poly[[{μ₂‐1,4‐bis[(2‐methyl‐1H‐imidazol‐1‐yl)methyl]benzene}(μ₂‐glutarato)zinc(II)] tetrahydrate], {[Zn(C₅H₆O₄)(C₁₆H₁₈N₄)]·4H₂O}_n or {[Zn(Glu)(1,4‐mbix)]·4H₂O}_n ( II ), have been synthesized hydrothermally using glutarate (Glu^2?) mixed with 1,4‐bis[(2‐methyl‐1H‐imidazol‐1‐yl)methyl]benzene (1,4‐mbix), and characterized by single‐crystal X‐ray diffraction, IR and UV–Vis spectroscopy, powder X‐ray diffraction, and thermogravimetric and photoluminescence analyses. Ni^II MOF ( I ) shows a 4‐connected 3D framework with point symbol 6⁶, but is not a typical dia network. Zn^II MOF ( II ) displays a two‐dimensional 4⁴‐ sql network with one‐dimensional water chains penetrating the grids along the c direction. The solid‐state photoluminescence analysis of ( II ) was performed at room temperature and the MOF exhibits highly selective sensing toward Fe³⁺ and Cr₂O₇^2? ions in aqueous solution.     

Three Coordination Polymers based on 3,5‐Bis(imidazole‐1‐yl)pyridine and Benzoic Acid: Synthesis,Crystal Structures and Photoluminescent Properties

Three metal coordination polymers {[Co(L)₂(H₂O)₂]²⁺ · 2NO₃^–}_n ( 1 ), {[Mn(L)₂(H₂O)₂]²⁺ · 2Cl^– · 3H₂O}_n ( 2 ), and [ZnL(ba)₂]_n ( 3 ) [L = 3,5‐bis(imidazole‐1‐yl)pyridine and Hba = benzoic acid] were synthesized and structurally characterized by IR spectroscopy, elemental analysis, X‐ray powder diffraction, and X‐ray single crystal diffraction. Complex 1 shows a one‐dimensional (1D) chain structure. Adjacent chains are connected by hydrogen bonding and nitrate groups to form a 3D network. Complex 2 features a 2D layer structure. A three‐dimensional network is constructed through the cluster consisting of two chloride ions and three water molecules. Complex 3 shows a 1D zigzag chain structure that further twists together to form a 3D network. The X‐ray powder diffraction patterns were compared with the simulated ones. Moreover, the luminescent properties of 1 – 3 were investigated in the solid state at room temperature, and the thermogravimetric analyses were carried out to study the thermal stability of the three complexes.     

Copper‐based Metal‐organic Framework for Non‐enzymatic Electrochemical Detection of Glucose

A non‐enzymatic electrochemical glucose sensor based on a Cu‐based metal‐organic framework (Cu‐MOF) modified electrode was developed. The Cu‐MOF was prepared by a simple ionothermal synthesis, and the characterizations of the Cu‐MOF were studied by Fourier transform infrared spectroscopy (FT‐IR), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), single‐crystal X‐ray powder diffraction (SCXRD), and X‐ray powder diffraction (XRD). Electrochemical behaviors of the Cu‐MOF modified electrode to glucose were measured by differential pulse voltammetry (DPV). The electrochemical results showed that the Cu‐MOF modified electrode exhibited an excellent electro‐catalytic oxidation towards glucose in the range of 0.06 μM to 5 mM with a sensitivity of 89 μA/mM cm² and a detection limit of 10.5 nM. Moreover, the fabricated sensor showed a high selectivity to the oxidation of glucose in coexistence with other interferences. The sensor was satisfactorily applied to the determination of glucose in urine samples. With the significant electrochemical performances, MOFs may provide a suitable platform in the construction of kinds of electrochemical sensors and/or biosensors and hold a great promise for sensing applications.     

Three New Lanthanide Coordination Polymers Built from H2bpdc Ligands: Syntheses,Structures, and Properties

Three new lanthanide‐organic coordination polymers, {[Ln₂(bpdc)₂(H₂O)₆(NO₃)] · NO₃} [Ln = La ( 1 ), Ce ( 2 ), Pr ( 3 )] (H₂bpdc = 2, 2′‐bipyridine‐6, 6′‐dicarboxylic acid) were synthesized under hydrothermal conditions and structurally characterized by elemental analysis, IR spectroscopy as well as single‐crystal and powder X‐ray diffraction. Single‐crystal X‐ray diffraction analysis revealed that compounds 1 – 3 are isostructural, composed of two dimensional honeycomb network linked by bpdc ligands. The magnetic property of compound 3 was investigated.     

A 3D 12‐Ring Zeolite with Ordered 4‐Ring Vacancies Occupied by (H2O)2 Dimers

A germanate zeolite, PKU‐14, with a three‐ dimensional large‐pore channel system was structurally characterized by a combination of high‐resolution powder X‐ray diffraction, rotation electron diffraction, NMR, and IR spectroscopy. Ordered Ge₄O₄ vacancies inside the [4⁶.6¹²] cages has been found in PKU‐14, in which a unique (H₂O)₂ dimer was located at the vacancies and played a structure‐directing role. It is the first time that water clusters are found to be templates for ordered framework vacancies.     

Crystal‐to‐Crystal Transformation: An HgII Metal–Organic Polymer Constructed with a Triazole Ligand

A new one‐dimensional double‐chain Hg^II coordination polymer containing the ligand 3,5‐bis(4‐pyridyl)‐4‐amino‐1,2,4‐triazole (bpatrz) and thiocyanate anions, namely, {[Hg₂(μ‐bpatrz)(μ‐SCN)₂(SCN)₂] · MeOH}_n ( 1 ), has been synthesized and structurally characterized by single‐crystal X‐ray diffraction. Compound 1 displays bright blue luminescence with emission maxima around 370 and 440 nm in solution and the solid state, respectively. Uptake and release of MeOH by 1 were investigated by powder X‐ray diffraction, thermogravimetric analysis, elemental analysis, and IR and NMR spectroscopy.     

A 3D Metal‐organic Framework Containing [Cd(3‐CPOA)]n (3‐CPOA2– = 3‐Carboxyphenoxyacetato Dianion) Expanded by 4,4′‐Bipyridine

The hydrothermal reaction of Cd(NO₃) · 4H₂O with 4,4′‐bipyridine (bipy) and 3‐carboxyphenoxyacetatic acid (3‐H₂CPOA) afforded a 3D metal‐organic framework (MOF) [Cd(3‐CPOA)(bipy)]_n · 3.5nH₂O, which was characterized by elemental analyses, IR spectroscopy, thermogravimetric analyses, and X‐ray diffraction. The single‐crystal structural analysis revealed that it has a Cds‐type topological network with 1D channels that contain encapsulated water molecular tapes.