Metal-Organic Frameworks

Version	Summary	Created by	Modification	Content Size	Created at	Operation
1		Catherine Raptopoulou	+ 6012 word(s)	6012	2021-01-12 05:14:08	\|
2	format correct	Vivi Li	+ 1 word(s)	6013	2021-01-13 05:23:08	\|

This entry is adapted from the peer-reviewed paper 10.3390/ma14020310

Metal-organic frameworks represent a porous class of materials that are build up from metal ions or oligonuclear metallic complexes and organic ligands. They can be considered as sub-class of coordination polymers and can be extended into one-dimension, two-dimensions, and three-dimensions. Depending on the size of the pores, MOFs are divided into nanoporous, mesoporous, and macroporous items. The latter two are usually amorphous. MOFs display high porosity, a large specific surface area, and high thermal stability due to the presence of coordination bonds. The pores can incorporate neutral molecules, such as solvent molecules, anions, and cations, depending on the overall charge of the MOF, gas molecules, and biomolecules. The structural diversity of the framework and the multifunctionality of the pores render this class of materials as candidates for a plethora of environmental and biomedical applications and also as catalysts, sensors, piezo/ferroelectric, thermoelectric, and magnetic materials.

metal-organic frameworks coordination polymers synthesis applications

1. Introduction

Metal Organic Frameworks (MOFs) constitute a class of solid porous materials, which consist of metal ions or metallic clusters, which act as nodes, and polydentate organic ligands, which act as linkers between the nodes. The metal nodes (metal ions or metallic clusters) act as connection points and the organic ligands bridge the metal centers through coordination bonds, thus, forming networks of one-dimension, two-dimensions, or three-dimensions. The main structural features of the MOFs, which are directly related to their properties and applications, are the high porosity, the large volume of the pores, which can reach the 90% of the crystalline volume or more, the large specific surface area (several thousand m²·g⁻¹), and the high thermal stability (250–500 °C) due to the presence of strong bonds (e.g., C–C, C–H, C–O, and M–O). An important sub-class of MOFs are the Isoreticular Metal Organic Frameworks (IRMOFs), which were first synthesized by the group of Yaghi ^[1]. The archetype IRMOF-1 was based on octahedral Zn-O-C clusters and 1,4-benzenedicarboxylic acid (BDC) bound to form a network with pcu topology. The series of IRMOFs retain the pcu topology and are based on varied organic linkers resulting in variable pore volumes and surface area. According to the terminology officially adopted by IUPAC on 2013 ^[2], MOFs are a sub-class of coordination networks (i.e., coordination compounds which extend to one-dimension, two-dimensions, or three-dimensions through repeating coordination entities), which are a sub-class of coordination polymers (i.e., coordination compounds with repeating coordination entities extending in 1, 2, or 3 dimensions, which do not need to be crystalline). MOFs are dynamic systems susceptible to structural changes upon external stimuli, such as temperature and pressure, and may not be crystalline.

The chemistry of MOFs has evolved rapidly in recent decades and it has become possible to adjust the size and shape of the pores, the network topology, and their surface area, so that the structures and properties of MOFs can be adapted to the needs of each application. The designed synthesis of new MOFs with desired physical and chemical properties in terms of Crystal Engineering principles requires the understanding of molecular and/or intermolecular interactions within the three-dimensional arrangement. The molecular interactions are the coordination bonds between the metal ions and the organic ligands, whereas the intermolecular interactions are the weak interactions such as hydrogen bonds, π–π interactions, etc. The designed synthesis of MOFs also requires complete control of the components and tools to be used, which is a fact that has been strongly argued by many researchers who believe that the complete control of all parameters of a chemical reaction is not feasible. On the other hand, lies the argument of the designed synthesis of IRMOFs, based on MOF-5, which resulted in a fairly large series of solids.

The structural characteristics of the MOFs are mainly affected by the large number of coordination geometries adopted by the metal ions and the use of oligonuclear metal clusters as nodes (secondary building units, SBUs), the geometrical characteristics, and the flexibility of the organic ligands, the role of the counterions, and the reaction solvent ^[3]^[4]^[5]^[6]^[7]. The network topology and dimensionality of the MOFs are strictly related to the different coordination geometries that can be adopted by the metal nodes, which vary depending on the electronic structure of the metal ions. Transition metal ions, especially those of the first row, lanthanides, and alkaline earth metals have been used because they display a wide variety of coordination numbers, geometries, and oxidation states, thus, offering synthetic and structural diversity. The use of rigid or flexible organic ligands plays a very important role in designing a MOF because the flexible ligands offer increased degrees of freedom with respect to the rigid ones and can lead to unpredictable crystal structures ^[8]. Organic molecules containing one or more N-donor or O-donor atoms are normally used as organic ligands to bridge between the metal ions in MOFs. Carboxylates (either aliphatic or aromatic containing one or more rings), pyridyl (e.g., pyrazine and 4.4′-bipyridyl derivatives) and cyano compounds, polyamines resulting from imidazole, oxalic acid, and benzene, phosphonates, sulfonates, and crown ethers are the most common ligands used. The anions counterbalance the positive charge of cationic MOFs and influence the supramolecular structure either being coordinated to the metal ions or by occupying the pores of the structure ^[9]. Organic cations can be hosted within the pores of anionic MOFs and can be exchanged by other cations, as in the case of bio-MOF-1, which hosts Me₂NH₂⁺ cations and solvate molecules and retains its crystallinity in solvent exchange experiments as well as during storage and release of cationic drug molecules ^[10]. Metal cations are usually coordinated to the original network, thus, altering its structural characteristics, whereas anionic metallic clusters require large porous structures and, in exceptional cases, can be exchanged by other cations for sensor applications ^[11]. The reaction solvent can affect the crystallization kinetics and the network topology through steric effects, fill coordination sites of the metal ions, complete the pores of the MOF, or participate in weak intermolecular interactions contributing to the crystal and thermal stability of the lattice.

The three-dimensional structure of MOFs is formed due to strong coordination bonds between the metal ions and the organic ligands and displays cavities and inner surfaces, which are occupied by counterions, guest molecules, and/or solvate molecules. Other types of interactions, such as hydrogen bonds, metal-metal bonds, and π–π interactions can occur and contribute to the stability of the MOFs. However, coordination bonds are stronger and provide more stable networks. Depending on the size of the cavities/pores, the MOFs are divided into nanoporous materials, with pores less than 20 Å in diameter, mesoporous materials (20–500 Å in diameter), and macroporous materials (over 500 Å in diameter). Most of the mesoporous and macroporous MOFs are amorphous materials ^[12]. Increasing the size of the pores is still a challenge since interpenetration prevents the presence of free empty space in a network. Interpenetration is favored by organic ligands with aromatic rings capable of the development of π–π interactions. Highly porous MOFs have been prepared by using poly-carboxylato and rigid alkyne-type ligands, as well as SBUs with large dimensions, which determine the size of the pores ^[13].

2. Applications of MOFs

MOFs display a range of structural features, namely large surface area, high porosity, crystallinity and thermal stability, and functionality of pores and frameworks, which render them promising materials for environmental and biomedical applications, as catalysts, sensors, absorbers for toxic gases, and metal ions.

2.1. Gas Adsorption/Separation/Storage for Energy and Environmental Applications

MOFs have been extensively studied for applications in gas storage. For example, H₂ and CH₄ represent alternative energy resources for future vehicles, and their effective usage still remains a challenge for the automotive industry. The capture of toxic industrial gases, such as NH₃ and H₂S, and volatile hydrocarbons, like benzene, as well as the removal of SO₂ and NO_x from flue gas, are of great importance for environmental protection. A very critical step in the chemical industry is the separation of mixtures of gases, such as CO₂ capture and CO₂/CH₄, CO₂/N₂ separation, O₂ purification, and so on.

CO₂ is the main greenhouse gas and is responsible for global warming and for water acidification. MOF-74-Mg, which is the magnesium analogue of MOF-74, shows the highest CO₂ uptake capacity of 228 and 180 cm³·g⁻¹ at 273 and 298 K and 1 bar, respectively (Figure 1) ^[14]. The exceptional CO₂ uptake by MOF-74-Mg is attributed to the increased ionic character of the Mg-O bond, which imparts additional uptake beyond weight effects while maintaining the reversibility of adsorption. MOF-210 has a very high surface area of 10,450 m²·g⁻¹ and shows a CO₂ uptake value of 2400 mg·g⁻¹ (74.2 wt %, 50 bar at 298 K), which is larger than that of MOF-177 or MIL-101(Cr) (60 wt % and 56.9 wt %, respectively) ^[15]^[16]^[17]. MOF-200 has a similar CO₂ uptake as MOF-210 under similar conditions. Other MOFs, which show considerably higher CO₂ uptake compared with other solid materials, are the NU-100 (69.8 wt %, 40 bar at 298 K), the MOF-5 (58 wt %, 10 bar at 273 K), and the HKUST-1 (19.8 wt %, 1 bar at 298 K).

Figure 1. (a) The 1D channels of MOF-74-Mg, Mg-DOBDC (solvents omitted). (b) Space-filling model of the pore structure of MOF-74-Mg (Mg, green. C, grey. O, red). (c) PXRD data for the isostructural MOFs M-DOBDC (M = Zn, Co, Mg, Ni). (d) CO₂ sorption isotherm (296K, 0 to 1 atm) of the isostructural MOFs M-DOBDC (inset: CO₂ sorption isotherms at 296 K, 0 to 0.1 atm). Reprinted with permission from J. Am. Chem. Soc. 2008, 130, 10870–10871 (^[14]). Copyright 2008 American Chemical Society.

Synthetic strategies for the preparation of MOFs with efficient CO₂ uptake capacity have been developed and include amine incorporation, introduction of functional groups, and additional metal ions and control of pore size. The method used in the industry for CO₂ separation is the amine scrubbing, which is high-energy consuming and presents disadvantages, such as amine degradation and equipment corrosion. Alternatively, MOFs incorporating amines have been examined as potential candidates for CO₂ separation. For example, incorporation of N,N′-dimethylethylenediamine (mmen) within the [Mg₂(dobpdc)] MOF (dobpdc⁴⁻ = 4,4′-dioxido-3,3′-biphenyldicarboxylate) afforded [mmen-Mg₂(dobpdc)], which displays an exceptional capacity for CO₂ adsorption at low pressures, 2.0 mmol·g⁻¹ (8.1 wt %) at 0.39 mbar, and 25 °C and 3.14 mmol·g⁻¹ (12.1 wt %) at 0.15 bar and 40 °C, at conditions relevant to removal of CO₂ from air and flue gas, respectively ^[18]. In addition, [en-Mg₂(dobpdc)] and [dmen-Mg₂(dobpdc)] (en = ethylenediamine, dmen = N,N′-dimethylethylenediamine) display significant CO₂ uptakes (3.63 mmol·g⁻¹ and 3.77 mmol·g⁻¹, respectively) at 0.15 bar ^[19]. Bio-MOF-11, [Co₂(ad)₂(CH₃CO₂)₂]·2dmf·0.5H₂O (ad⁻ = adeninate) contains pyrimidine and amino groups within the pores of the framework and exhibits high CO₂ capacity (~6 mmol·g⁻¹ at 273 K) and exceptional selectivity for CO₂ over N₂ at 273 K (81:1) and 298 K (75:1) ^[20]. MOFs functionalized with low-molecular weight polymers containing amino groups, such as PEI (polyethyleneimine), have shown impressive CO₂ uptake, which were many times larger than the respective MOFs. For example, PEI-MIL-101-125 display CO₂ uptake of 3.95 and 4.51 mmol·g⁻¹, respectively, over four times than that of MIL-101-125, and PEI@UiO-66 shows CO₂ uptake up to 1.65 mmol·g⁻¹ and CO₂/CH₄ selectivity 111, which are much larger values than UiO-66 ^[21]^[22]. Yaghi and co-workers reported the functionalization of the organic ligand of IRMOF-74-III with primary amine through ligand modification, thus, yielding six analogs with different functional groups (–CH₃, –NH₂, –CH₂NHBoc, –CH₂NMeBoc, –CH₂NH₂, and –CH₂NHMe). Spectroscopic data revealed that CO₂ binds chemically to IRMOF-74-III-CH₂NH₂ and IRMOF-74-III-CH₂NHMe to form carbamic species. The CO₂ uptake of IRMOF-74-III-CH₂NH₂ is 3.2 mmol·g⁻¹ at 800 Torr and 298 K ^[23]. Introduction of polar functional groups in the pores of MOFs through direct synthesis or post-synthesis modification was proved an efficient method to enhance the adsorption capacity and selectivity of CO₂. For example, UPC-12 exhibits high selectivity for CO₂ due to the formation of H-bonds between the CO₂ molecules and the -COOH groups within the pores and the π–π stacking interactions between the CO₂ molecules and the bpy moieties of the MOF ^[24]. NbO-type MOFs retain the NbO-type structure upon functionalization with different groups, such as amide, nitro groups, and N-heterocycles, and display higher CO₂ uptake than the parent MOFs ^[25]^[26]^[27]^[28]^[29]. Ligand functionalized UiO-66, UiO-66(Zr)-(COOH)₂ shows high CO₂/N₂ selectivity of 56 upon a 15/85 CO₂/N₂ gas mixture at 303 K and 1 bar, and UiO-67 functionalized BUT-10 and BUT-11 show enhanced CO₂ adsorption uptakes (50.6 and 53.5 cm³·g⁻¹, respectively) and separation selectivity over N₂ and CH₄ (18.6 and 31.5 for a 15/85 CO₂/N₂ gas mixture, and 5.1 and 9.0 for a 10/90 CO₂/CH₄ gas mixture) ^[30]^[31]. The control of the pore size of the MOFs allows inclusion of smaller guests (e.g., CO₂ 3.30 Å) and enables ultra-high selectivity. However, the precise control of pores with a size of 3–4 Å is very difficult. Examples of isoreticular MOFs, SIFSIX-2-Cu, SIFSIX-2-Cu-i, SIFSIX-3-Zn, and SIFSIX-3-Cu showed more efficient CO₂ capture for the latter, which exhibits the smallest pore size ^[32]^[33]. The approach of ‘Single Molecule Trap’ (SMT) for the capture of a single CO₂ molecule was developed by Zhou and co-workers who prepared paddlewheel dicopper complexes (SMT-1-2) with intramolecular metal-metal distance of 7.4 Å, suitable for the accommodation of one CO₂ molecule. Incorporation of SMT-1 to the 3D framework of PCN-88 enhanced the CO₂ uptake to 4.20 mmol·g⁻¹ at 296 K and 1 bar with respect to 0.63 mmol·g⁻¹ for SMT-1 under identical conditions ^[34]. MOFs based on heterometallic SBUs of the general formula [M^II₂M^III(OH)(COO)₆], CPM-200s, display excellent CO₂ uptake capacity, 207.6 and 190.9 cm³·g⁻¹ for CPM-200-Fe/Mg and CPM-200-In/Mg, respectively, at 273 K and 1 bar, comparable to the value of MOF-74-Mg ^[35]. Other examples of heterometallic MOFs such as MIL-101(Cr,Mg) and UiO-66(Li,Na,K,Pb) display higher CO₂ uptake with respect to the parent MOF, but is much smaller than MOF-74-Mg and CPM-200s, which hold the highest values ^[36]^[37]^[38]^[39]. The mixed-metal solid-solution MOFs [(AlOH)_1−x(VO)_xL] (x = 0–1, L = 1,4-benzenedicarboxylate) display a total uptake of 11–14 mmol·g⁻¹ at 1 bar for the low vanadium content species, which is comparable with the values found for other members of the MIL-53 family ^[40].

Light hydrocarbon separation is a very important and crucial process in the petroleum industry, and their efficient separation will reduce the energy consumption and cost. Ethylene (C₂H₄) and propylene (C₃H₆) are used in the production of polymers. During the production of C₂H₄, an impurity of ~1% of C₂H₂ is also produced. The microporous MOF [Cu(atbdc)] (H₂atbdc = 5-(5-amino-1H-tetrazol-1-yl)-1.3-benzenedicarboxylic acid), UTSA-100, displays high C₂H₂/C₂H₄ selectivity and high C₂H₂ uptake from mixtures containing 1% acetylene. At 296 K and 1 atm, the acetylene and ethylene uptake amount of UTSA-100 are 95.6 and 37.2 cm³·g⁻¹, respectively, which is much higher than that of M’MOF-3 ^[41]^[42]. Other examples of MOFs exhibiting high C₂H₂ uptake are UTSA-300 (3.41 mmol·g⁻¹ at 273 K and 1 bar) ^[43], SIFSIX-1-Cu (8.50 mmol·g⁻¹ at 298 K and 1 bar) ^[44], [Mn₃(bipy)₃(H₂O)₄][Mn(CN)₆]·2(bipy)·4H₂O (3.2 mmol·g⁻¹ at 27–83 K and 1 bar) ^[45], and NOTT-300 (6.34 mmol·g⁻¹ at 293 K and 1 bar) ^[46]. In addition, the raw propylene (C₃H₆) product contains trace impurity of propyne (C₃H₄), which is highly undesirable. Chen and co-workers reported a flexible-robust MOF, ELM-12, which shows strong binding affinity and suitable pore confinement for propyne, and obtained propylene with a purity over 99.9998%, which is the propyne impurity removed to a concentration below 2 ppm ^[47]. The separation of C₂H₄ and C₃H₆ from their mixtures with the respective alkanes by using distillation processes shows low efficiency because of the similarity of their boiling points. Their separation can be alternatively achieved by the formation of π-complexes of olefins with transition metal cations ^[48]^[49], and by using MOFs, such as KAUST-7, which contains channels allowing the adsorption of C₃H₆ but does not permit the C₃H₈ to diffuse/adsorb into the pore system ^[50]^[51]. Another important and difficult process in the chemical industry is the separation of benzene and cyclohexane, as well as C₂H₂/CO₂ separation. Conventional distillation is high energy consuming. Therefore, alternative methods involving the use of suitable MOFs containing open metal sites, or introducing π–π stacking interactions of the π-electron deficient pore surface and π-rich guest molecules have been developed ^[52]^[53]^[54]^[55].

Alternative technologies for H₂ storage and its potential use as renewable fuel for vehicle applications have long explored during the early years of MOFs development. The required materials should meet the U.S. Department of Energy (DOE) requirements, which are 5.5 wt % H₂ gravimetric capacity achievable in the temperature range of −40 to 60 °C with a maximum pressure of 100 bar. Well-known MOFs, such as MOF-5, MOF-177, and UiO-66 display H₂ uptake 5 wt % (77 K, 90 bar), 7.5 wt % (77 K, 80 bar), and 4.2 wt % (77 K, 60 bar), respectively ^[56]^[57]^[58]. Recent advances include the synthesis of a series of Pd-doped MIL-101 samples with different Pd content affecting their H₂ storage performances, Pt nanoparticles on the outer surface of MOF-5, and then coating with hydrophobic microporous carbon black (CB/Pt/MOF-5 composite), which displays 41% higher H₂ uptake than that of MOF-5, incorporation of polarized organic units into MOFs to improve the binding energy of H₂ (e.g., MOF-649 and MOF-650 with internally polarized 2,6-azulenedicarboxylate), and carbon nanodots functional MOFs, Cdots@UMCM-1a, with efficiently enhanced H₂ storage capacity attributed to specific interactions between the H₂ adsorbate and polar groups on the surface of the Cdots ^[59]^[60]^[61]^[62].

Great progress has been made during recent decades on MOFs for applications on storage of CH₄, which is the primary component of natural gas. For vehicle applications, an ideal MOF should have both high CH₄ storage capacity and high CH₄ deliverable capacity. Promising examples, which meet the volumetric target set by DOE (263 cm³·cm⁻³ at 35 bar), are HKUST-1 with total uptake 267 and 272 cm³·cm⁻³ at 65 and 80 bar, respectively, and working capacity of 190 and 200 cm³·cm⁻³ at 65 and 80 bar, respectively, UTSA-76 with total uptake of 257 cm³·cm⁻³ at 65 bar, and working capacity of 197 cm³·cm⁻³ at 80 bar, Ni-MOF-74 with total uptake of 251 and 267 cm³·cm⁻³ at 65 and 80 bar, respectively, and working capacity of 129 and 152 cm³·cm⁻³ at 65 and 80 bar, respectively, NJZU-53 with total uptake 241 cm³·cm⁻³ at 65 bar, and working capacity of 190 cm³·cm⁻³ at 65 bar, PCN-14 with total uptake of 230 and 250 cm³·cm⁻³ at 65 and 80 bar, respectively, and working capacity of 157 and 178 cm³·cm⁻³ at 65 and 80 bar, respectively, and MOF-519 with total uptake of 279 cm³·cm⁻³ at 80 bar, and working capacity of 230 cm³·cm⁻³ at 80 bar (Figure 2) ^[63]^[64]^[65]^[66].

Figure 2. Methane uptake properties (green) and working capacity (red) of selected MOFs. Reprinted with permission from J. Am. Chem. Soc. 2013, 135, 11887–11894 (^[64]). Copyright 2013 American Chemical Society.

2.2. Sensing Applications

MOFs are especially attractive as novel sensing materials because they display a high surface area, which enhances detective sensitivity, specific structural features (open metal sites, tunable pore sizes, etc.), which promote host-guest interactions and selectivity, and flexible porosity, which enables reversible release and uptake of small molecules, cations and anions, biomolecules, and so on. The guest molecules can induce visible changes including a shift of the emission spectrum or change in the emitting color, and change in the fluorescence intensity such as ‘turn-on’ and ‘turn-off’ processes.

A thermostable Mg-based MOF, [Mg(pdda)(dmf)] (H₂pdda = 4,4′-(pyrazine-2,6-diyl) dibenzoic acid), which contains nanoholes and non-coordinating nitrogen atoms inside the walls of the holes, displays high selectivity for Eu³⁺ ions at low concentrations in aqueous solutions ^[67]. A luminescent Ln-MOF, [Me₂NH₂][Tb(bptc)] (H₄bptc = 3,3′,5,5′-tetracarboxylic acid) exhibits rare chiral helical channels despite the achiral nature of the organic ligand. Luminescent studies showed highly selective fluorescence quenching response to Fe³⁺ ions in a liquid suspension, rendering it as a potential chemo-sensor for Fe³⁺ ions ^[68]. A bimetallic Eu-Tb MOF with 1,4-benzenedicarboxylate ligands showed Pb²⁺ selectivity in polluted environmental waters. The color of the luminescent Ln-MOFs could be fine-tuned from green to red by doping the MOFs with different Tb/Eu ratios, and, in the presence of Pb²⁺, the emission color of the MOFs changes from red-orange to green, which is visually observed by naked eyes ^[69]. A Cd-MOF, [Cd(edda)] (H₄edda = 5,5′-ethane-1,2-diylbis(oxy)]diisophthalic acid), exhibits ratiometric fluorescence response to Hg²⁺ for the first time with a fast response (~15 s) and especially high sensitivity of ~2 nM below the permissible limits in drinking water set by the U.S. Environmental Protection Agency. This behavior is attributed to the collapse of the crystal structure of the Cd-MOF induced by Hg²⁺ ^[70]. MOFs have been proven as very promising materials for the uranium extraction during radionuclide separation and seawater mining due to their ability for post grafting with functional groups with strong affinity for the uranium ions and porous functionalization for storage of hydrated U(IV) ions. HKUST-1, UiO-66, MILs, and ZIF-8 display stability under gamma irradiation. The phosphoryl-urea-functionalized UiO-68(Zr) MOF was the first organo-modified MOF that exhibited uranium extraction behavior. Examples of phosphonate-functionalized, amidoxime-functionalized, amine-functionalized MOFs, among others, display adsorption capacity up to 360 mg·g⁻¹ ^[71].

Volatile organic molecules and explosive compounds can be efficiently detected by MOFs based on guest-dependent luminescent responses either by shifting of the emission spectrum or by changes in the luminescent intensity ^[72]^[73]^[74].

Various anions have been successfully detected by MOF-based sensors. [Ln₂(bpdc)(bdc)₂(H₂O)₂] (Ln = Eu, Tb; H₂bpdc = 2,2′-bipyridine-3,3′-dicarboxylic acid) can detect F⁻ ions based on a significant decrease in fluorescence, and [Ln₂Zn(L)₃(H₂O)₄](NO₃)₂ (Ln = Eu, Tb; L = 4,4′-dicarboxylate-2,2′-dipyridine anion) shows high selectivity and sensitivity to I⁻ ions ^[75]^[76]. An Ln-mucinate MOF shows CO₃²⁻ sensing ability through the greatest luminescence enhancement over other anions, and MOF-based thin-film show selectivity on CO₃²⁻ over other anions, e.g., SO₄²⁻, PO₄³⁻, ClO₄⁻, etc., in aqueous solution through a turn-off response ^[77]^[78]. The highly toxic CrO₄²⁻ and Cr₂O₇²⁻ anions found in wastewater can be efficiently detected by MOFs, such as [Ln₄(OH)₄(bpdc)₃(bpdca)₀.₅(H₂O)₆](ClO₄) (Ln = Tb, Gd, bpdca²⁻ = biphenyl-4,4′-dicarboxylate), and [Cd(tptz)(H₂O)₂(HCOOH)(ipa)₂] (tptz = {4-[4-(1H-1,2,4-triazol-1-yl)phenyl]phenyl}-1H-1,2,4-triazole, ipa = isophthalic acid) ^[79]^[80]. The cationic MOF [CuL₂(H₂O)₀.₅](NO₃)₂ displays characteristic colors in response to specific anions, such as Cl⁻, Br⁻, I⁻, SCN⁻, and N₃⁻ (Figure 3) ^[81]. The isostructural heterometallic MOFs, In/Eu-CBDA, and In/Tb-CBDA (CBDA = 5,5′-(carboxylbis(azanediyl))-diisophthalic acid) can detect 1,4-dinitrobenzene and Cr₂O₇²⁻ with high selectivity and sensitivity ^[82]. ZnO quantum dots on MOF-5 is an effective fluorescent sensing platform for the phosphates tested for the assessment of phosphates in environmental aqueous samples ^[83], and CdSe/CdS/Cd₀.₅Zn₀.₅S/ZnS quantum dots on MOF-5, QD@MOF-5 composite display size-selective thiol sensing ^[84].

Figure 3. Color change of [CuL₂(H₂O)₀.₅](NO₃)₂ (1′) upon exchange of nitrates by the indicated anions. Chem. Commun. 2012, 48, 2946–2948 (^[81])—Reproduced by permission from The Royal Society of Chemistry.

MOF-based sensors for humidity measurements have been studied based on changes of fluorescence or electrochemical signals, such as CuMOF, thin-film of HKUST-1, Cu-BTC film, and amine-functionalized MOF nanoparticles NH₂-MIL-125(Ti) ^[85]^[86]^[87]^[88]^[89]. pH and temperature sensors based on luminescent MOFs have been extensively studied for monitoring pH changes in biological environments and for luminescent thermometers. For example, among others, [Eu₃(C₁₄H₆N₂O₄)₄(OH)(H₂O)₄]·2H₂O displays a linear photoluminescence response in the 5–7.5 pH range, UiO-66-N=N-ind_3h synthesized by post-synthetic modification of UiO-66-NH₂ exhibits pH-dependent fluorescence in the 1–12 pH range, (Tb-THBA) nanoparticles (THBA = tris[(2-hydroxy-benzoyl)-2-aminoethyl]amine) show a temperature-dependent luminescent intensity in the range of 20–65 °C, and [Zn₃(TDPAT)(H₂O)₃] (TDPAT = 2,4,6-tris(3,5-dicarboxylphenylamino)-1,3,5-triazine) can detect a temperature from 164 to 276 K ^[90]^[91]^[92]^[93].

Core-shell nanocomposites with an MOF core have been developed for sensing biological molecules, such as human serum albumin, bacterial endospores, and cancer cell apoptosis ^[94]^[95]^[96]. Luminescent MOFs are also successful in detecting DNA, RNA, protein, and other biomolecules and present advantages over other sensing materials for biomolecules (e.g., single-walled carbon nanotubes, graphene oxide, carbon nanoparticles, gold nanoparticles), such as structural diversity, high sensitivity, and biodegradability. Biocompatibility and non-toxic metal clusters need to be developed in order for in vivo sensing to be realized ^[97].

2.3. Catalytic Applications

MOFs have been extensively used as heterogeneous catalysts for the synthesis of fine chemicals, which are extremely important in the chemical industry. The properties that render MOFs suitable for heterogeneous catalysts are related to the robust nature, which is required for catalysis under extreme conditions, the porosity, and large surface area, which facilitated the catalytic activity as well as the presence of pores and channels, which are needed for catalytic selectivity and the organic ligands that can tune the catalytic reactivity and selectivity. The catalytic active sites of MOFs may be the metal nodes, the functionalized ligands, and the pores of the structure. The synthesis of fine chemicals is most commonly realized through oxidation reactions (e.g., epoxidation, sulfoxidation, aerobic oxidation), 1,3-cycloaddition reactions, transesterification reactions, C–C bond formation reactions (e.g., Heck reaction, Sonogashira coupling, and Suzuki coupling), and hydrogenation reactions of unsaturated organic molecules. The MOFs as heterogeneous catalysts may act as Lewis acids through the metal ions or metal nodes as well as the organic ligands, or as support for the moieties that carry the oxygen or the noble metals necessary for the catalytic reaction. The Zn MOF-5 was partially substituted with manganese and the bimetallic MnFe-MOF-74 was used for the epoxidation of the alkene with high selectivity (up to 99%, Figure 4) ^[98]^[99]. Composites of metal complexes immobilized on MOF can also act as Lewis acids in epoxidation reactions, such as post synthetically modified (Cr)NH₂-MIL-101, post synthetically modified UiO-66 and UiO-67 with salicylaldehyde molybdenum complex, and copper functionalized UiO-66 ^[100]^[101]^[102]. The aerobic oxidation of alcohols to aldehydes or ketones requires the presence of noble metals inside the pores of the MOF or attachment to the modified ligands. Palladium and gold nanoparticles introduced into the nanoporous MOF are used for selective aerobic oxidation ^[103]^[104]. Cu-based MOFs are usually used as catalysts for 1,3-dipolar cycloaddition reactions, which is the formation of five-membered ring compounds ^[105]^[106]. Several examples of MOF catalysts in transesterification reactions have been reported, such as UiO-66 and UiO-67 ^[107]^[108]. C-C bond formation reactions such as Heck reactions, Sonogashira coupling, and Suzuki coupling are extremely important for organic synthesis and require the presence of palladium or palladium nanoparticles as catalysts, which are incorporated in the pores or are attached to the functionalized organic ligands. For example, palladium complexes, such as bis(tri(1-piperidinyl)phosphine) palladium chloride or bis(triphenylphosphine) palladium dichloride incorporated in a Ni-MOF for the Heck reaction of estragole with iodobenzene ^[109], palladium incorporated in a Zr-MOF based on 2,2′-bipyridine-5,5′-dicarboxylate ligands applied in the carbonylative Sonogashira coupling at atmospheric pressure in the presence of CO ^[110], and palladium dichloride immobilized on a mixed-ligand MOF containing bipyridyl and biphenyl moieties for Suzuki catalysis ^[111]. Palladium nanoparticles incorporated in Zr MOF-808 is an excellent heterogeneous catalyst for Heck reaction without an additional base ^[112], whereas palladium nanoclusters in NH₂-UiO-66 (Zr) used in the Suzuki catalysis in the presence of light give 99% conversion and selectivity of biphenyl compounds ^[113]. A wide range of unsaturated organic compounds, such as α,β-unsaturated aldehydes, cinnamaldehyde, nitroarene, and nitro compounds, alkenes and alkynes, quinoline, benzene, and other aromatic compounds, can be hydrogenated with a very high yield and selectivity under mild conditions in the presence of MOFs and derived materials as heterogeneous catalysts. For example, Pt nanoparticles incorporated within MIL-101(Fe,Cr) used as catalysts for the hydrogenation of α,β-unsaturated aldehydes to unsaturated alcohols ^[114]. MIL-120 incorporated with Ni particles showed a better result on gas-phase benzene hydrogenation than the Ni/Al₂O₃ catalyst ^[115], which is a well-defined hollow Zn/Co ZIF composite with rhombic dodecahedron shape that displayed superior activity and selectivity toward the semi-hydrogenation of acetylene ^[116], and Ir nanoparticles encapsulated in ZIF-8 used in the hydrogenation of phenylacetylene ^[117]. The catalytic activity for the CO₂→CO reduction with [Ru₃(btc)_2-x(pydc)_xX_y] catalysts (X = Cl, OH, OAc, x = 0.1, 0.2, 0.6, 1.0; 0 ≤ y ≤ 1.5, H₃btc = benzene-1,3,5-tricarboxylic acid, H₂pydc = pyridine-3,5-dicarboxylic acid) as monitored by UHV-FTIR spectroscopy, showed peaks characteristic of the presence of (CO)Ru^δ+ species. The CO₂→CO conversion at 90 K is attributed to charge transfer from the 3d Ru orbitals to the 2π_u CO₂ antibonding orbital, possibly yielding chemisorbed CO₂^δ− species that might act as a reaction intermediate to produce CO ^[118]. These defect-engineered MOFs also act as olefin hydrogenation catalysts after activation with H₂ to produce Ru-H species, assisted by the presence of the basic pyridyl-N atom of the pydc linkers ^[118]. Cu-based MOFs, [Cu₃(btc)₂] HKUST-1 (btc³⁻ = benzene-1,3,5-tricarboxylate) and [Cu₃(btb)₂] MOF-14 (btb³⁻ = benzene-1,3,5-tribenzoate) display high catalytic activity toward CO oxidation at low temperatures (105 K), which is related to the CO species adsorbed on the Cu²⁺ coordinatively unsaturated metal ion sites upon exposure to various amounts of O₂ ^[119]. Several MOFs, for example NU-1000, UiO-66, HKUST-1, and MIL-101(Cr)-DAAP, have been tested as heterogeneous catalysts for the catalytic destruction of the phosphate ester bonds and phosphate-fluoride bonds, in chemical warfare agents, such as DMNP (dimethyl 4-nitrophenyl phosphate), DENP (diethyl 4-nitrophenyl phosphate), BNPP (bis(4-nitrophenyl) phosphate), and the highly toxic GD (O-pinacolyl methylphosphonofluoridate), known as Soman ^[120].

Figure 4. Schematic view of the selective catalytic activity of MnFe-MOF-74 for the epoxidation of the cyclic alkenes in the presence of ^tBuSO₂PhIO. Reprinted with permission from ACS Catal., 2018, 8, 596–601 (^[98]). Copyright 2018 American Chemical Society.

Two-dimensional MOFs have been recently developed as catalysts of outstanding intrinsic reactivity, as support materials for catalysts, and as catalysts with multifunctional catalytic activity for diverse organic transformations. Their enhanced catalytic activity is associated with the ultra-thin thickness and more accessible active sites, which decrease the diffusion resistance and increase the host-guest interactions, rendering these materials much better than the corresponding bulk MOFs ^[121]. For example, 2D MOFs based on tetrakis(4-carboxyphenyl)-porphyrin display unique photochemistry and high efficiency in light-harvesting applications and showed catalytic activity in photooxidation reactions (Figure 5) ^[122]^[123]^[124]. Incorporation of nanoparticles or enzymes as well as post-synthetic modification provided new materials with enhanced catalytic activities ^[125]. For example, [Zr₁₂O₈(OH)₁₄(BPYDC)₉] (H₂BPYDC = 2,2′-bipyridine-5,5′-dicarboxylic acid), MON-19, loaded with platinum nanoparticles, displays efficient hydrogenation of C=C bonds under mild conditions without external high-pressure hydrogen ^[126].

Figure 5. (a) Schematic representation of a single-layered 2D nanosheet of Cu-MOF. Color code: C, gray. O, red. S, yellow. F, green. Cu polyhedral, blue. H-atoms not shown. (b) Schematic representation of a Cu(II) center in the nanosheets. (c) Molecular structure of a-chymotrypsin. (d) The polychrome sections in this structure are the active site with residues Asp-102, His-57, and Ser-195. a-chymotrypsin can be effectively inhibited by 2D Cu-MOF, [Cu(bpy)OTf)₂] (bpy = 4,4′-bipyridine, OTf = trifluoromethanesulfonate). Reprinted with permission from J. Am. Chem. Soc., 2017, 139, 8312–8319 (^[122]). Copyright 2018 American Chemical Society.

2.4. Piezo/Ferroelectric, Thermoelectric, and Dielectric Applications

The piezoelectric materials convert mechanical energy into electrical energy through the direct piezoelectric effect and can be considered as energy harvesters to generate energy when direct electricity or batteries are not available. A subclass are the ferroelectric materials, which exhibit spontaneous electric polarization whose direction can be reversed by applying external electric fields. Piezo/ferroelectric materials, such as crystalline and ceramic materials, polymers, and liquid crystals find potential applications in piezoelectric quartz crystals as ultrasonic transducer, sensors and actuators, filters, ultrasonic motors, energy harvester, optical devices and so on. Besides traditional piezo/ferroelectric materials, MOFs have investigated for potential applications, among these [Zn₂(mtz)(nic)₂(OH)]·0.5H₂O (Hmtz = 5-methyltetrazole, Hnic = nicotinic acid), [Zn(phtz)(nic)]₂ (Hphtz = 5-phenyltetrazole), [Cd(tib)(p-BDC-OH)]·H₂O (tib = 1,3,5-tris(1-imidazolyl)benzene, p-BDC-OH = 2-OH-1,4-benzenedicarboxylic acid), [In(C₁₆H₁₁N₂O₈]·1.5H₂O, and [Mn₅(NH₂bdc)₅(bimb)₅]·0.5H₂O (NH₂bdcH₂ = 2-amino-1,4-benzene dicarboxylic acid, bimb = 4,4′-bis(1-imidazolyl)biphenyl) show significant ferroelectric properties with spontaneous polarization values of P_s of 6.26, 5.27, 11.65, 3.81, and 2.556 μC·cm⁻², respectively ^[127]^[128]^[129]^[130]. The piezoelectric properties of MOFs have been rarely studied. For example, a MOF based on [Cd(imazethpyr)] displays a piezoelectric coefficient d₃₃ value of 60.10 pC·N⁻¹, which is smaller than that of BaTiO₃, but was the first MOF with such piezo/ferroelectricity (Figure 6) ^[131]. ZIF-8-based MOFs exhibit ‘soft’ piezo/ferroelectricity and water soluble MOFs such as NUS-series and UiO-series exhibit piezoelectric coefficient as d_zz up to 3.5 pm·V⁻¹ ^[132]^[133]^[134].

Figure 6. (a) The diamond-like net of MOF based on [Cd(imazethpyr)] and (b) electric hysteresis loop of the MOF. Dalton Trans. 2008, 3946–3948 (^[131])—Reproduced by permission of The Royal Society of Chemistry.

The thermoelectric materials, which can generate electric potential from a temperature difference, constitute an environmentally-friendly approach of energy generation from waste heat. Besides inorganic compounds, such as oxides and alloys, the approach of conductive MOFs as new potential thermoelectric materials has been developed. This approach includes first-row transition metal MOFs with thiolate ligands, such as [Cu(pdt)₂] (pdt = 2,3-pyrazinedithiolate), inclusion of guest molecules in known MOFs, such as TCNQ@HKUST-1 (HKUST-1 = [Cu₃(BTC)₂], BTC = benzene tricarboxylate), I₂ and metal nanoclusters in order to improve the conductivity of the material. 2D MOF nanosheets of bis(thiolato) ligands and light transition metals, i.e., π-d conjugated systems, and post-synthetically modified MOFS, i.e., guest@MOFs and conductive-polymer grafted MOFs, are promising candidates for the fabrication of thermoelectric devices due to their excellent conductivity ^[135].

Semiconducting devices are based on dielectric materials, which display ultra-low dielectric constants (κ < 3.9 as in SiO₂). MOFs feature ultra-low dielectric constants, which are considered as promising materials for the future microelectronics industry. The requirements of doing so are thermal stability at a high temperature, predictable mechanical behavior, electrical insulation, and adhesion to other interlayers. DFT calculation on various MOFs, such as IRMOF-1 family, UiO-66, UiO-67, MIL-140, and MOF-74-M (M = Mg, Mn, Fe, Co, Ni, Zn), revealed the influence of the structural and chemical characteristics on their electronic and dielectric properties, demonstrating their ability to behave as insulators and low-dielectric constant materials, and predicted dielectric constants in the range of 1.25 to 2.0 ^[136]^[137]. Surface-anchored HKUST-1 thin films grown by liquid phase epitaxy (LPE) were studied by spectroscopic ellipsometry (SE) to determine an optical constant of n = 1.39 at a wavelength of 750 nm (κ~1.93) ^[138]. ZIF-8 thin films deposited on silicon wafers studied by SE and the dielectric constant was measured by impedance analysis at different frequencies and temperatures yielding κ = 2.33 at 100 kHz ^[139]. Other MOFs, which display ultra-low dielectric constants (below that of SiO₂) are, for example, [Sr₂(1,3-dbc)₂(H₂O)₂] (bdc = 1,3-bis(4,5-dihydro-2-oxazolyl)benzene), which retains its crystallinity up to 420 °C with κ~2.4 ^[140], [Zn₂(Hbbim)₂(bbim)] (H₂bbim = bisbenzimidazole) with κ~3.05 ^[141], [Pb(tab)₂(4,4′-bipy)](PF₆) (tab = 4-(trimethylammonio)benzenethiolate) with κ~2.53, [Zn₂(L-trp)₂(bpe)₂(H₂O)₂] (L-trp = L-tryptophane, bpe = 1,2-bis(4-pyridyl)ethylene) with κ~2.53, [Mn₂(D-cam)₂(2-Hpao)₄] (D-cam = D-camphoric acid, 2-Hpao = 2-pyridinealdoxime) with κ~2.8, and [Co₂(D-cam)₂(3-abpt)₂(H₂O)₃] (3-abpt = 4-amino-3,5-bis(3-pyridyl)-1,2,4-triazole) with κ~3.0 ^[142].

2.5. Proton-Conducting and Magnetic Materials

Recently, MOFs have attracted considerable interest as proton-conducting materials and their potential applications in electrochemical devices, sensors, hydrogen fuel cells, etc. MOFs can accommodate various proton carriers in their pores/channels and can provide useful insight into the proton-conducting pathway and mechanism, and these advantages render them excellent materials for such applications. While the negative charge of the lattice is not a prerequisite for conducting protons, many of them are anionic MOFs whose charge is offset by small protonated amines or protons attached to the solvent molecules by hydrogen bonds, or protons weakly attached to functional groups of the ligands (less frequently in carboxylates, more often in sulfonic and phosphonate ligands). For example, {H[(N(CH₃)₄)₂][Gd₃(NIPA)₆]}·3H₂O (H₂NIPA = 5-nitroisophthalic acid) displays high proton conductivity of 7.17 × 10⁻² S·cm⁻¹ at high relative humidity, which is among the highest values for proton-conducting MOFs ^[143], and the bimetallic complex {NH(prol)₃}[MnCr(ox)₃] (NH(prol)₃⁺ = tri(3-hydroxypropyl)ammonium, ox = oxalate), which consists of oxalate-bridged bimetallic layers interleaved by NH(prol)₃⁺ ions and shows proton conduction of ~10⁻⁴ S·cm⁻¹ under 75% relative humidity due to the presence of an extensive H-bonded network between the anionic MOF, the NH(prol)₃⁺ ions, and water molecules ^[144]. Some examples of neutral MOFs, which display high proton conductivity, are [Tb₄(TTHA)₂(H₂O)₄]·7H₂O (H₆TTHA = 1,3,5-triazine-2,4,6-triamine hexaacetic acid) with high proton conductivity over 10⁻² S·cm⁻¹ at 295–358 K temperature range due to an extensive H-bond network formed between water solvates and carboxyl groups ^[145], [Ln(L)(H₂O)₂] (Ln^III = Dy, Er, Gd; H₃L = (HO)₂P(O)CH₂CO₂H) with proton conductivity values of 1.13 × 10⁻⁶, 2.73 × 10⁻³, and 6.27 × 10⁻⁶ S·cm⁻¹, respectively, at high temperatures (>348 K) and 95% relative humidity ^[146], and [Ln₂(CO₃)(ox)₂(H₂O)₂]·3H₂O (Ln^III = Ce, Pr, Nd, Tb) with proton conductivity above 10⁻³ S·cm⁻¹ without an additional humidity (Figure 7) ^[147].

Figure 7. The 3D framework of {[Gd₂(CO₃)(ox)₂(H₂O)₂]·3H₂O, which contains an ordered one-dimensional pore channel along the a-axis, which serves as a 1D hydrogen bond pathway. The compound shows high proton conductivity (up right) and a large magnetocaloric effect (down right). Reprinted with permission from Inorg. Chem. 2018, 57, 9020–9027 (^[147]). Copyright 2018 American Chemical Society.

References

Britt, D.; Tranchemontagne, D.; Yaghi, O.M. Metal-organic frameworks with high capacity and selectivity for harmful gases. Proc. Natl. Acad. Sci. USA 2008, 105, 11623–11627.
Batten, S.R.; Champness, N.R.; Chen, X.-M.; Garcia-Martinez, J.; Kitagawa, S.; Öhrström, L.; O’Keeffe, M.; Paik Suh, M.; Reedijk, J. Terminology of metal–organic frameworks and coordination polymers (IUPAC Recommendations 2013). Pure Appl. Chem. 2013, 85, 1715–1724.
Aakeroy, C.B.; Champness, N.R.; Janiak, C. Recent advances in crystal engineering. CrystEngComm 2010, 12, 22–43.
Kato, M.; Fujihara, T.; Yano, D.; Nagasawa, A. Anion influence on the coordination polymer structures of silver(I) complexes with 2-methylisothiazol-3(2H)-one. CrystEngComm 2008, 10, 1460–1466.
Sague, J.L.; Meuwly, M.; Fromm, K.M. Counterion effect on the formation of coordination polymer networks between AgNO3 and L (2,2′-oxybis(ethane-2,1-diyl) diisonicotinate). CrystEngComm 2008, 10, 1542–1549.
Noro, S.-I.; Horike, S.; Tanaka, D.; Kitagawa, S.; Akutagawa, T.; Nakamura, T. Flexible and shaphe-selective guest binding at CuII axial sites in 1-dimensional CuII-1,2-bis(4-pyridyl-ethane) coordination polymers. Inorg. Chem. 2006, 45, 9290–9300.
Paz, F.A.A.; Klinowski, J.; Vilela, S.M.F.; Tome, J.P.C.; Cavaleiro, J.A.S.; Rocha, J. Ligand design for functional metal-organic frameworks. Chem. Soc. Rec. 2012, 41, 1088–1110.
Lazarou, K.N.; Psycharis, V.; Terzis, A.; Raptopoulou, C.P. Network diversity and supramolecular isomerism in copper(II)/1,2-bis(4-pyridyl)ethane coordination polymers. Polyhedron 2011, 30, 963–970.
Noro, S.-I.; Kitaura, R.; Kondo, M.; Kitagawa, S.; Ishii, T.; Matsuzaka, H.; Yamashita, M. Framework engineering by anions and porous functionalities of Cu(II)/4,4′-bpy coordination polymers. J. Am. Chem. Soc. 2002, 124, 2568–2583.
An, J.; Geib, S.J.; Rosi, N.L. Cation-triggered drug release from a porous zinc-adeninate metal-organic framework. J. Am. Chem. Soc. 2009, 131, 8376–8377.
Wang, Y.; Wang, X.-G.; Yuan, B.; Shao, C.-Y.; Chen, Y.-Y.; Zhou, B.-b.; Li, M.-S.; An, X.-M.; Cheng, P.; Zhao, X.-J. Cation-exchange porosity tuning in a dynamic 4d-4f-3d framework for NiII ion-selective luminescent probe. Inorg. Chem. 2015, 54, 4456–4465.
Férey, G.; Haouas, M.; Loiseau, T.; Taulelle, F. Nanoporous solids: How do they form? An in situ approach. Chem. Mater. 2014, 26, 299–309.
Cronin, L.; Kögerler, P.; Müller, A. Controlling growth of novel solid-state materials via discrete molybdenum-oxide-based building blocks as synthons. J. Solid State Chem. 2000, 152, 57–67.
Caskey, S.R.; Wong-Foy, A.G.; Matzger, A.J. Dramatic tuning of carbon dioxide uptake via metal substitution in a coordination polymer with cylindrical pores. J. Am. Chem. Soc. 2008, 130, 10870–10871.
Furukawa, H.; Ko, N.; Go, Y.B.; Aratani, N.; Choi, S.B.; Choi, E.; Yazaydin, A.O.; Snurr, R.Q.; O’Keeffee, M.; Kim, J.; et al. Ultrahigh porosity in metal-organic frameworks. Science 2010, 329, 424–428.
Wong-Foy, A.G.; Matzger, A.J.; Yaghi, O.M. Exceptional H2 saturation uptake in microporous metal-organic frameworks. J. Am. Chem. Soc. 2006, 128, 3494–3495.
Ferey, G.; Mellot-Draznieks, C.; Serre, C.; Millange, F.; Dutour, J.; Surble, S.; Margiolaki, I. A chromium terephthalate-based solid with unusually large pore volume and surface area. Science 2005, 309, 2040–2042.
McDonald, T.M.; Lee, W.R.; Mason, J.A.; Wiers, B.M.; Hong, C.S.; Long, J.R. Capture of carbon dioxide from air and flue gas in the alkylamine-appended metal-organic framework mmen-Mg2(dobpdc). J. Am. Chem. Soc. 2012, 134, 7056–7065.
Jo, H.; Lee, W.R.; Kim, N.W.; Jung, H.; Lim, K.S.; Kim, J.E.; Kang, D.W.; Lee, H.; Hiremath, V.; Seo, J.G.; et al. Fine-tuning of the carbon dioxide capture capability of diamine-grafted metal-organic framework adsorbents through amine functionalization. ChemSusChem 2017, 10, 541–550.
An, J.; Geib, S.J.; Rosi, N.L. High and selective CO2 uptake in a cobalt adeninate metal-organic framework exhibiting pyrimidine- and amino-decorated pores. J. Am. Chem. Soc. 2010, 132, 38–39.
Lin, Y.; Yan, Q.; Kong, C.; Chen, L. Polyethyleneimine incorporated metal-organic frameworks adsorbent for highly selective CO2 capture. Sci. Rep. 2013, 3, 1859.
Xian, S.; Wu, Y.; Wu, J.; Wang, X.; Xiao, J. Enhanced dynamic CO2 adsorption capacity and CO2/CH4 selectivity on polyethyleneimine-impregnated UiO-66. Ind. Eng. Chem. Res. 2015, 54, 11151–11158.
Fracaroli, A.M.; Furukawa, H.; Suzuki, M.; Dodd, M.; Okajima, S.; Gandara, F.; Reimer, J.A.; Yaghi, O.M. Metal-organic frameworks with precisely designed interion for carbon dioxide capture in the presence of water. J. Am. Chem. Soc. 2014, 136, 8863–8866.
Wang, R.; Liu, X.; Qi, D.; Xu, Y.; Zhang, L.; Liu, X.; Jiang, J.; Dai, F.; Xiao, X.; Sun, D. A Zn metal-organic framework with high stability and sorption selectivity for CO2. Inorg. Chem. 2015, 54, 10587–10592.
Zheng, B.; Liu, H.; Wang, Z.; Yu, X.; Yi, P.; Bai, J. Porous NbO-type metal-organic framework with inserted acylamide groups exhibiting highly selective CO2 capture. CrystEngComm 2013, 15, 3517–3520.
Zhang, M.; Wang, Q.; Lu, Z.; Liu, H.; Liu, W.; Bai, J. A nitro-decorated NbO-type metal-organic framework with a highly selective CO2 uptake and CH4 storage capacity. CrystEngComm 2014, 16, 6287–6290.
Song, C.; He, Y.; Li, B.; Ling, Y.; Wang, H.; Feng, Y.; Krishna, R.; Chen, B. Enhanced CO2 sorption and selectivity by functionalization of a Nb-O type metal-organic framework with polarized benzothiadiazole moieties. Chem. Commun. 2014, 50, 12105–12108.
Song, C.; Ling, Y.; Jin, L.; Zhang, M.; Chen, D.-L.; He, Y. CO2 adsorption of three isostructural metal-organic frameworks depending on the incorporated highly polarized heterocyclic moieties. Dalton Trans. 2016, 45, 190–197.
Mu, Q.; Wang, H.; Li, L.; Wang, C.; Wang, Y.; Zhao, X. Enhanced CO2 adsorption affinity in a NbO-type MOF constructed from a low-cost diisophthalate ligand with a piperazine-ring bridge. Chem. Asian J. 2015, 10, 1864–1869.
Yang, Q.; Vaesen, S.; Ragon, F.; Wiersum, A.D.; Wu, D.; Lago, A.; Devic, T.; Martineau, C.; Taulelle, F.; Llewellyn, P.L.; et al. A water stable metal-organic framework with optimal features for CO2 capture. Angew. Chem. Int. Ed. 2013, 52, 10316–10320.
Wang, B.; Huang, H.; Lv, X.-L.; Xie, Y.; Li, M.; Li, J.-R. Tuning CO2 selective adsorption over N2 and CH4 in UiO-67 analogues through ligand functionalization. Inorg. Chem. 2014, 53, 9254–9259.
Nugent, P.; Belmabkhout, Y.; Burd, S.D.; Cairns, A.J.; Luebke, R.; Forrest, K.; Pham, T.; Ma, S.; Space, B.; Wojtas, L.; et al. Porous materials with optimal adsorption thermodynamis and kinetics for CO2 separation. Nature 2013, 495, 80–84.
Shekhah, O.; Belmabkhout, Y.; Chen, Z.; Guillerm, V.; Cairns, A.; Adil, K.; Eddaoudi, M. Made-to-order metal-organic frameworks for trace carbon dioxide removal and air capture. Nat. Commun. 2014, 55, 4228.
Li, J.-R.; Yy, J.; Lu, W.; Sun, L.-B.; Sculley, J.; Balbuena, P.B.; Zhou, H.-C. Porous materials with pre-designed single-molecule traps for CO2 selective adsorption. Nat. Commun. 2013, 4, 1538.
Zhai, Q.-G.; Bu, X.; Mao, C.; Zhao, X.; Feng, P. Systematic and dramatic tuning on gas sorption performance in heterometallic metal-organic frameworks. J. Am. Chem. Soc. 2016, 138, 2524–2527.
Zhou, Z.; Mei, L.; Ma, C.; Xu, F.; Xiao, J.; Xia, Q.; Li, Z. A novel bimetallic MIL-101(Cr,Mg) with high CO2 adsorption capacity and CO2/N2 selectivity. Chem Eng. Sci. 2016, 147, 109–117.
Hu, Z.; Zhang, K.; Zhang, M.; Guo, Z.; Jiang, J.; Zhao, D. A combinatorial approach towards water-stable metal-organic frameworks for highly efficient carbon dioxide separation. ChemSusChem 2014, 7, 2719–2795.
Hu, Z.; Lin, J.; Ogiwara, N.; Rodriguez, A.; Peng, Y.; Wang, Y.; Horike, S.; Zhao, D. A pH-responsive phase transformation of a sulfonated metal-organic framework from amorphous to crystalline for efficient CO2 capture. CrystEngComm 2016, 18, 2803–2807.
Hu, Z.; Faucher, S.; Zhuo, Y.; Sun, Y.; Wang, S.; Zhao, D. Combination of optimization and metalated-ligand exchange: An effective approach to functionalize UiO-66(Zr) MOFs for CO2 separation. Chem. Eur. J. 2015, 21, 17246–17255.
Kozachuk, O.; Meilikhov, M.; Yusenk, K.; Schneemann, A.; Jee, B.; Kuttatheyil, A.V.; Bertmer, M.; Sternemann, C.; Pöppl, A.; Fischer, R.A. A solid-solution approach to mixed-metal metal-organic frameworks—Detailed characterization of local structures, defects and breathing behavior of Al/V frameworks. Eur. J. Inorg. Chem. 2013, 4546–4557.
Xiang, S.-C.; Zhang, Z.; Zhao, C.-G.; Hong, K.; Zhao, X.; Ding, D.-R.; Xie, M.-H.; Wu, C.-D.; Das, M.C.; Gill, R.; et al. Rationally tuned micropores within enantiopure metal-organic frameworks for highly selective separation of acetylene and ethylene. Nat. Commun. 2011, 2, 204.
Hu, T.-L.; Wang, H.; Li, B.; Krishna, R.; Wu, H.; Zhou, W.; Zhao, Y.; Han, Y.; Wang, X.; Zhu, W.; et al. Microporous metal-organic framework with dual functionalities for highly efficient removal of acetylene from ethylene/acetylene mixtures. Nat. Commun. 2015, 6, 7328.
Lin, R.-B.; Li, L.; Wu, H.; Arman, H.; Li, B.; Lin, R.-G.; Zhou, W.; Chen, B. Optimized separation of acetylene from carbon dioxide and ethylene in a microporous material. J. Am. Chem. Soc. 2017, 139, 8022–8028.
Cui, X.; Chen, K.; Xing, H.; Yang, Q.; Krishna, R.; Bao, Z.; Wu, H.; Zhou, W.; Dong, X.; Han, Y.; et al. Pore chemistry and size control in hybrid porous materials for acetylene capture from ethylene. Science 2016, 353, 141–144.
Hazra, A.; Jana, S.; Bonakala, S.; Balasubramanian, S.; Maji, T.K. Separation/purification of ethylene from an acetylene/ethylene mixtrure in a pillared-layer porous metal-organic framework. Chem. Commun. 2017, 53, 4907–4910.
Yang, S.; Ramirez-Cuesta, A.J.; Newby, R.; Garcia-Sakai, V.; Manuel, P.; Callear, S.K.; Campbell, S.I.; Tang, C.C.; Schröder, M. Supramolecular binding and separation of hydrocarbons within a functionalized porous metal-organic framework. Nat. Chem. 2015, 7, 121–129.
Li, L.; Lin, R.-B.; Krishna, R.; Wang, X.; Li, B.; Wu, H.; Li, J.; Zhou, W.; Chen, B. Flexible-robust metal-organic framework for efficient removal of propyne from propylene. J. Am. Chem. Soc. 2017, 139, 7733–7736.
Uchida, S.; Kawamoto, R.; Tagami, H.; Nakagawa, Y.; Mizuno, N. Highly selective sorption of small unsaturated hydrocarbons by nonporous flexible framework with silver ion. J. Am. Chem. Soc. 2008, 130, 12370–12376.
Zhang, Y.; Li, B.; Krishna, R.; Wu, Z.; Ma, D.; Shi, Z.; Pham, T.; Forrest, K.; Space, B.; Ma, S. Highly selective adsorption of ethylene over ethane in a MOF featuring the combination of open metal site and π-complexation. Chem. Commun. 2015, 51, 2714–2717.
Yaghi, O.M.; O’Keeffe, M.O.; Ockwig, N.W.; Chae, H.K.; Eddaoudi, M.; Kim, J. Reticular synthesis and the design of new materials. Nature 2003, 423, 705–714.
Cadiau, A.; Adil, K.; Bhatt, P.M.; Belmabkhout, Y.; Eddaoudi, M. A metal-organic framework-based splitter for separating prolylene from propane. Science 2016, 353, 137–140.
Mukherjee, S.; Manna, B.; Desai, A.V.; Yin, Y.; Krishna, R.; Babarao, R.; Ghosh, S.K. Harnessing Lewis acidic open metal sites of metal-organic frameworks: The foremost route to achieve highly selective benzene sorption over cyclohexane. Chem. Commun. 2016, 52, 8215–8218.
Cheng, J.-Y.; Wang, P.; Ma, J.-P.; Liu, Q.-K.; Dong, Y.-B. A nanoporous Ag(I)-MOF showing unique selective adsorption of benzene among its organic analogues. Chem. Commun. 2014, 50, 13672–13675.
Manna, B.; Mukherjee, S.; Desai, A.V.; Sharma, S.; Krishna, R.; Ghosh, S.K. A π-electron deficient diaminotriazine functionalized MOF for selective sorption of benzene over cyclohexane. Chem. Commun. 2015, 51, 15386–15389.
Joarder, B.; Mukherjee, S.; Chaudhari, A.K.; Desai, A.V.; Manna, B.; Ghosh, S.K. Guest-responsive function of a dynamic metal-organic framework with a π Lewis acidic pore surface. Chem. Eur. J. 2014, 20, 15303–15308.
Gygi, D.; Bloch, E.D.; Mason, J.A.; Hudson, M.R.; Gonzalez, M.I.; Siegelman, R.L.; Darwish, T.A.; Queen, W.L.; Brown, C.M.; Long, J.R. Hydrogen storage in the expanded pore metal-organic frameworks M2(dobpdc) (M = Mg, Mn, Fe, Co, Ni, Zn). Chem. Mater. 2016, 28, 1128–1138.
Chae, H.K.; Seberio-Perez, D.Y.; Kim, J.; Go, Y.-B.; Eddaoudi, M.; Matzger, A.J.; O’Keefee, M.; Yaghi, O.M. A route to high surface area, porosity and inclusion of large molecules in crystals. Nature 2004, 427, 523–527.
Abid, H.R.; Tian, H.; Ang, H.-M.; Tade, M.O.; Buckley, C.E.; Wang, S. Nanosize Zr-metal organic framework (UiO-66) for hydrogen and carbon dioxide storage. Chem. Eng. J. 2012, 187, 415–420.
Qin, W.; Cao, W.; Liu, H.; Li, Z.; Li, Y. Metal-organic framework MIL-101 doped with palladium for toluene adsorption and hydrogen storage. RSC Adv. 2014, 4, 2414–2420.
Kim, J.; Yeo, S.; Jeon, J.-D.; Kwak, S.-Y. Enhancement of hydrogen storage capacity and hydrostability of metal-organic frameworks (MOFs) with surface-loaded platinum nanoparticles and carbon black. Microporous Mesoporous Mater. 2015, 202, 8–15.
Barman, S.; Khutia, A.; Koitz, R.; Blacque, O.; Furukawa, H.; Iannuzzi, M.; Yaghi, O.M.; Janiak, C.; Hutter, J.; Berke, H. Synthesis and hydrogen adsorption properties of internally polarized 2,6-azulenedicarboyxlate based metal-organic frameworks. J. Mater. Chem. A 2014, 44, 18823–18830.
Li, J.-S.; Tang, Y.-J.; Li, S.-L.; Zhang, S.-R.; Dai, Z.-H.; Si, L.; Lan, Y.-Q. Carbon nanodots functional MOFs composites by a stepwise synthetic approach: Enhanced H2 storage and fluorescent sensing. CrystEngComm 2015, 17, 1080–1085.
Spanopoulos, I.; Tsangarakis, C.; Klontzas, E.; Tylianakis, E.; Froudakis, G.; Adil, K.; Belmabkhout, Y.; Eddaoudi, M.; Trikalitis, P.N. Reticular synthesis of HKUST-like tbo-MOFs with enhanced CH4 storage. J. Am. Chem. Soc. 2015, 138, 1568–1574.
Peng, Y.; Krungleviciute, V.; Eryazici, I.; Hupp, J.T.; Farha, O.K.; Yildirim, T. Methane storage in metal-organic frameworks: Current records, surprise findings, and challenges. J. Am. Chem. Soc. 2013, 135, 11887–11894.
Li, B.; Wen, H.-M.; Wang, H.; Wu, H.; Tyagi, M.; Yildirim, T.; Zhou, W.; Chen, B. A porous metal-organic framework with dynamic pyrimidine groups exhibiting record high methane storage working capacity. J. Am. Chem. Soc. 2014, 136, 6207–6210.
Song, C.; Liu, H.; Jiao, J.; Bai, D.; Zhou, W.; Yildirim, T.; He, Y. High methane storage and working capacities in a NbO-type metal-organic framework. Dalton Trans. 2016, 45, 7559–7562.
Gao, Y.; Zhang, X.; Sun, W.; Liu, Z. A robust microporous metal-organic framework as a highly selective and sensitive, instantaneous and colorimetric sensor for Eu3+ ions. Dalton Trans. 2015, 44, 1845–1849.
Zhao, X.-L.; Tian, D.; Gao, Q.; Sun, H.-W.; Xu, J.; Bu, X.-H. A chiral lanthanide metal-organic framework for selective sensing of Fe(III) ions. Dalton Trans. 2016, 45, 1040–1046.
Zeng, X.; Zhang, Y.; Zhang, J.; Hu, H.; Wu, X.; Long, Z.; Hou, Z. Facile colorimetric sensing of Pb2+ using bimetallic lanthanide metal-organic frameworks as luminescent probe for field screen analysis of lead-polluted environmental water. Microchem. J. 2017, 134, 140–145.
Wu, P.; Liu, Y.; Liu, Y.; Wang, J.; Li, Y.; Liu, W.; Wang, J. Cadmium-based metal-organic framework as a highly selective and sensitive ratiometric luminescent sensor for mercury(II). Inorg. Chem. 2015, 54, 11046–11048.
Xiong, J.; Fan, Y.; Luo, F. Grafting functional groups in metal-organic frameworks for U(IV) sorption from aqueous solutions. Dalton Trans. 2020, 49, 12536–12545.
Yi, F.-Y.; Chen, D.; Wu, M.-K.; Han, L.; Jiang, H.-L. Chemical sensors based on metal-organic frameworks. ChemPlusChem 2016, 81, 675–690.
Shi, Z.-Q.; Ji, N.-N.; Hu, H.-L. Luminescent triphenylamine-based metal-organic frameworks: Recent advances in nitroaromatics detection. Dalton Trans. 2020, 49, 12929–12939.
Kaur, R.; Paul, A.K.; Deep, A. Nanocomposite of europium organic framework and quantum dots for highly sensitive chemosensing of trinitrotoluene. Forensic Sci. Int. 2014, 242, 88–93.
Zhou, J.-M.; Shi, W.; Xu, N.; Cheng, P. Highly selective luminescent sensing of fluoride and organic small-molecule pollutants based on novel lanthanide metal-organic frameworks. Inorg. Chem. 2013, 52, 8082–8090.
Shi, P.-F.; Hu, H.-C.; Zhang, Z.-Y.; Xiong, G.; Zhao, B. Heterometal-organic frameworks as highly sensitive and highly selective luminescent probes to detect I− ions in aqueous solutions. Chem. Commun. 2015, 51, 3985–3988.
Wong, K.-L.; Law, G.-L.; Yang, Y.-Y.; Wong, W.-T. A highly porous luminescent terbium-organic framework for reversible anion sensing. Adv. Mater. 2006, 18, 1051–1054.
Liu, H.; Wang, H.; Chu, T.; Yu, M.; Yang, Y. An electrodeposited lanthanide MOF thin film as a luminescent sensor for carbamate detection in aqueous solution. J. Mater. Chem. C 2014, 41, 8683–8690.
Zhou, J.-M.; Shi, W.; Li, H.-M.; Li, H.; Cheng, P. Experimental studies and mechanism analysis of high-sensitivity luminescent sensing of pollutional small molecules and ions in Ln4O4 cluster based microporous metal-organic frameworks. J. Phys. Chem. C 2014, 118, 416–426.
Wang, Y.; Cheng, L.; Liu, Z.-Y.; Wang, X.-G.; Ding, B.; Yin, L.; Zhou, B.-B.; Li, M.-S.; Wang, J.-X.; Zhao, X.-J. An ideal detector composed of two-dimensional Cd(II)-triazole frameworks for nitro-compound explosives and potassium dichromate. Chem. Eur. J. 2015, 21, 14171–14178.
Ma, J.-P.; Yu, Y.; Dong, Y.-B. Fluorene-based Cu(II)-MOF: A visual colorimetric anion sensor and separator based on an anion-exchange approach. Chem. Commun. 2012, 48, 2946–2948.
Zhang, Y.; Ying, Y.; Feng, M.; Wu, L.; Wang, D.; Li, C. Two isostructural Ln3+-based heterometallic MOFs for the detection of nitro-aromatics and Cr2O72−. New J. Chem. 2020, 44, 12748–12754.
Zhao, D.; Wan, X.; Song, H.; Hao, L.; Su, Y.; Lv, Y. Metal-organic frameworks (MOFs) combined with ZnO quantum dots as a fluorescent sensing platform for phosphate. Sens. Actuators B Chem. 2014, 197, 50–57.
Falcaro, P.; Hill, A.J.; Nairn, K.M.; Jasieniak, J.; Mardel, J.I.; Bastow, T.J.; Mayo, S.C.; Gimona, M.; Gomez, D.; Whitfield, H.J.; et al. A new method to position and functionalize metal-organic framework crystals. Nat. Commun. 2011, 2, 237.
Yu, Y.; Zhang, X.-M.; Ma, J.-P.; Liu, Q.-K.; Wang, P.; Dong, Y.-B. Cu(I)-MOF: Naked-eye colorimetric sensor for humidity and formaldehyde in single-crystal-to-single-crystal fashion. Chem. Commun. 2014, 50, 1444–1446.
Yu, Y.; Ma, J.-P.; Dong, Y.-B. Luminescent humidity sensors based on porous Ln3+-MOFs. CrystEngComm 2012, 14, 7157–7160.
Liu, J.; Sun, F.; Zhang, F.; Wang, Z.; Zhang, R.; Wang, C.; Qiu, S. In situ growth of continuous thin metal-organic framework film for capacitive humidity sensing. J. Mater. Chem. 2011, 21, 3775–3778.
Robinsin, A.L.; Stavila, V.; Zeitler, T.R.; White, M.I.; Thornberg, S.M.; Greathouse, J.A.; Allendorf, M.D. Ultrasensitive humidity detection using metal-organic framework-coated microsensors. Anal. Chem. 2012, 84, 7043–7051.
Zhang, Y.; Chen, Y.; Zhang, Y.; Cong, H.; Fu, B.; Wen, S.; Ruan, S. A novel humidity sensor based on NH2-MIL-125(Ti) metal organic framework with high responsiveness. J. Nanoparticle Res. 2013, 15, 2014.
Harbuzaru, B.V.; Corma, A.; Rey, F.; Jorda, J.L.; Ananias, D.; Carlos, L.D.; Rocha, J. A miniaturized linear pH sensor based on a highly photoluminescent self-assembled europium(III) metal-organic framework. Angew. Chem. Int. Ed. Engl. 2009, 48, 6476–6479.
Aguilera-Sigalat, H.; Bradshaw, D. A colloidal water-stable MOF as a broad-range fluorescent pH sensor via post-synthetic modification. Chem. Commun. 2014, 50, 4711–4713.
Sun, L.-N.; Yu, J.; Peng, H.; Zhang, J.Z.; Shi, L.-Y.; Wolfbeis, O.S. Temperature-sensitive luminescent nanoparticles and films based on a terbium(III) complex probe. J. Phys. Chem. C 2010, 114, 12642–12648.
Ma, D.; Li, B.; Zhou, X.; Zhou, Q.; Liu, K.; Zeng, G.; Li, G.; Shi, Z.; Feng, S. A dual functional MOF as a luminescent sensor for quantitatively detecting the concentration of nitrobenzene and temperature. Chem. Commun. 2013, 49, 8964–8966.
Zhang, L.; Lei, J.; Ma, F.; Ling, P.; Liu, J.; Ju, H. A porphyrin photosensitized metal-organic framework for cancer cell apoptosis and caspase responsive theranostics. Chem. Commun. 2015, 51, 10831–10834.
Wang, X.; Wang, X.; Wang, Y.; Guo, Z. Terbium(III) complex as a luminescent sensor for human serum albumin in aqueous solution. Chem. Commun. 2011, 47, 8127–8129.
Ling, P.; Lei, J.; Zhang, L.; Ju, H. Porphyrin-encapsulated metal-organic frameworks as mimetic catalysts for electrochemical DNA sensing via allosteric switch of hairpin DNA. Anal. Chem. 2015, 87, 3957–3963.
Zhang, Q.; Wang, C.-F.; Lv, Y.-K. Luminescent switch sensors for the detection of biomolecules based on metal-organic frameworks. Analyst 2018, 143, 4221–4229.
Stubbs, A.W.; Braglia, L.; Borfecchia, E.; Meyer, R.J.; Roman-Leshkov, Y.; Lamberti, C.; Dinca, M. Selective Catalytic Olefin Epoxidation with MnII-Exchanged MOF-5. ACS Catal. 2018, 8, 596–601.
Yuan, K.; Song, T.; Wang, D.; Zou, Y.; Li, J.; Zhang, X.; Tang, Z.; Hu, W. Bimetal–organic frameworks for functionality optimization: MnFe-MOF-74 as a stable and efficient catalyst for the epoxidation of alkenes with H2O2. Nanoscale 2018, 10, 1591–1597.
Tabatabaeian, K.; Zanjanchi, M.A.; Mahmoodi, N.O.; Eftekhari, T.; Shafiei, S.M. Diimino Nickel Complex Anchored into the MOF Cavity as Catalyst for Epoxidation of Chalcones and Bischalcones. J. Clust. Sci. 2017, 28, 949–962.
Kaposi, M.; Cokoja, M.; Hutterer, C.H.; Hauser, S.A.; Kaposi, T.; Klappenberger, F.; Pöthig, A.; Barth, J.V.; Herrmanna, W.A.; Kühn, F.E. Immobilisation of a molecular epoxidation catalyst on UiO-66 and -67: The effect of pore size on catalyst activity and recycling. Dalton Trans. 2015, 44, 15976–15983.
Zhao, J.; Wang, W.; Tang, H.; Ramella, D.; Luan, Y. Modification of Cu2+ into Zr-based metal–organic framework (MOF) with carboxylic units as an efficient heterogeneous catalyst for aerobic epoxidation of olefins. Mol. Catal. 2018, 456, 57–64.
Akbari, S.; Mokhtari, J.; Mirjafari, Z. Solvent-free and melt aerobic oxidation of benzyl alcohols using Pd/Cu2(BDC)2DABCO–MOF prepared by one-step and through reduction by dimethylformamide. RSC Adv. 2017, 7, 40881–40886.
Wang, J.-S.; Jin, F.-Z.; Ma, H.-C.; Li, X.-B.; Liu, M.-Y.; Kan, J.-L.; Chen, G.-J.; Dong, Y.-B. Au@Cu(II)-MOF: Highly efficient bifunctional heterogeneous catalyst for successive oxidation–condensation reactions. Inorg. Chem. 2016, 55, 66856691.
Lu, B.-B.; Yang, J.; Che, G.-B.; Pei, W.-Y.; Ma, J.-F. Highly Stable Copper(I)-Based Metal–Organic Framework Assembled with Resorcin [4] arene and Polyoxometalate for Efficient Heterogeneous Catalysis of Azide–Alkyne “Click” Reaction. ACS Appl. Mater. Interfaces 2018, 10, 2628–2636.
Li, P.; Regati, S.; Huang, H.; Arman, H.; John, D.; Zhao, C.-G.; Chen, B. A metal-organic framework as a highly efficient and reusable catalyst for the solvent-free 1, 3-dipolar cycloaddition of organic azides to alkynes. Inorg. Chem. Front. 2015, 2, 42–46.
Liu, X.; Qi, W.; Wang, Y.; Su, R.; He, Z. Exploration of Intrinsic Lipase-Like Activity of Zirconium-Based Metal-Organic Frameworks. Eur. J. Inorg. Chem. 2018, 4579–4585.
Schumacher, W.T.; Mathews, M.J.; Larson, S.A.; Lemmon, C.E.; Campbell, K.A.; Crabb, B.T.; Chicoine, B.J.-A.; Beauvais, L.G.; Perry, M.C. Organocatalysis by site-isolated N-heterocyclic carbenes doped into the UiO-67 framework. Polyhedron 2016, 114, 422–427.
Tarnowicz-Ligus, S.; Augustyniak, A.; Trzeciak, A.M. Incorporation of PdCl2P2 Complexes in Ni-MOF for Catalyzing Heck Arylation of Functionalized Olefins. Eur. J. Inorg. Chem. 2019, 4282–4288.
Bai, C.H.; Jian, S.P.; Yao, X.F.; Li, Y.W. Carbonylative Sonogashira coupling of terminal alkynes with aryl iodides under atmospheric pressure of CO using Pd(II)@MOF as the catalyst. Catal. Sci. Technol. 2014, 4, 3261–3267.
Li, X.; Zeeland, R.V.; Maligal-Ganesh, R.V.; Pei, Y.; Power, G.; Stanley, L.; Huang, W. Impact of linker engineering on the catalytic activity of metal-organic frameworks containing Pd(II)-bipyridine complexes. ACS Catal. 2016, 6, 6324–6328.
Yan, X.; Wang, K.; Xu, X.; Wang, S.; Ning, Q.; Xiao, W.; Zhang, N.; Chen, Z.; Chen, C. Brönsted Basicity in Metal-organic Framework-808 and Its Application in Base-Free Catalysis. Inorg. Chem. 2018, 57, 8033–8036.
Sun, D.; Li, Z. Double-Solvent Method to Pd Nanoclusters Encapsulated inside the Cavity of NH2-UiO-66(Zr) for Efficient Visible-Light-Promoted Suzuki Coupling Reaction. J. Phys. Chem. C 2016, 120, 19744–19750.
Zhao, M.; Yuan, K.; Wang, Y.; Li, G.; Guo, J.; Gu, L.; Hu, W.; Zhao, H.; Tang, Z. Metal-organic frameworks as selectivity regulators for hydrogenation reactions. Nature 2016, 539, 76–80.
Wan, Y.; Chen, C.; Xiao, W.; Jian, L.; Zhang, N. Ni/MIL-120: An efficient metal-organic framework catalyst for hydrogenation of benzene to cyclohexane. Microporous Mesoporous Mater. 2013, 171, 9–13.
Yang, J.; Zhang, F.; Lu, H.; Hong, X.; Jiang, H.; Wu, Y.; Li, Y. Hollow Zn/CO ZIF particles derived from core-shell ZIF-67@ZIF-8 as selective catalyst for the semi-hydrogenation of acetylene. Angew. Chem. Int. Ed. Engl. 2015, 54, 10889–10893.
Zahmakirna, M. Iridium nanoparticles stabilized by metal organic frameworks (IrNPs@ZIF-8): Synthesis, structural properties and catalytic performance. Dalton Trans. 2012, 41, 12690–12696.
Kozachuk, O.; Luz, I.; Xamena, F.X.L.I.; Noei, H.; Kauer, M.; Albada, H.S.; Bloch, E.D.; Marler, B.; Qang, Y.; Muhler, M.; et al. Multifunctional, defect-engineered metal-organic frameworks with ruthenium centers: Sorption and catalytic properties. Angew. Chem. Int. Ed. Engl. 2014, 53, 7058–7062.
Noei, H.; Amirjalayer, S.; Müller, M.; Zhang, Z.; Schmid, R.; Muhler, M.; Fischer, R.A.; Wang, Y. Low-temperature CO oxidation over Cu-based metal-organic frameworks monitored by using FTIR spectroscopy. ChemCatChem 2012, 4, 755–759.
Mondloch, J.E.; Katz, M.J.; Isley III, W.C.; Ghosh, P.; Liao, P.; Bury, W.; Wagner, G.W.; Hall, M.G.; DeCoste, J.B.; Peterson, G.W.; et al. Destruction of chemical warfare agents using metal-organic frameworks. Nat. Mater. 2015, 14, 512–516.
Tan, C.; Liu, G.; Li, H.; Cui, Y.; Liu, Y. Ultrathin two-dimensional metal-organic framework nanosheets-and emerging class of catalytic nanomaterials. Dalton Trans. 2020, 49, 11073–11084.
Xu, M.; Yuan, S.; Chen, X.-Y.; Chang, Y.-J.; Day, G.; Gu, Z.-Y.; Zhou, H.-C. Two-dimensional metal-organic framework nanosheets as an enzyme inhibitor: Modulation of the α-chymotrypsin activity. J. Am. Chem. Soc. 2017, 139, 8312–8319.
He, T.; Ni, B.; Zhang, S.; Gong, Y.; Wang, H.; Gu, L.; Zhuang, J.; Hu, W.; Wang, X. Ultrathin 2D zirconium metal-organic framework nanosheets: Preparation and application in photocatalysis. Small 2018, 14, 1703929.
Xiao, Y.; Guo, W.; Chen, H.; Li, H.; Xu, X.; Wu, P.; Shen, Y.; Zheng, B.; Huo, F.; Wei, W.D. Ultrathin 2D Cu-porphyrin MOF nanosheets as a heterogeneous catalyst for styrene oxidation. Mater. Chem. Front. 2019, 3, 1580–1585.
Dhakshinamoorthy, A.; Asiri, A.M.; Garcia, H. Integration of metal organic frameworks with enzymes as multifunctional solids for cascade catalysis. Dalton Trans. 2020, 49, 11059–11072.
Zhou, Y.; Liu, Y.; Li, Z.; Huo, J.; Chen, C.; Li, Q.; Niu, S.; Wang, S. Regulating hydrogenation chemoselectivity of α, β-unsaturated aldehydes by combination of transfer and catalytic hydrogenation with ammonia borane and Pt/MOL. ChemSusChrm 2020, 13, 1746–1750.
Wen, L.L.; Zhou, L.; Zhang, B.G.; Meng, X.G.; Qu, H.; Li, D.F. Multifunctional amino-decorated metal–organic frameworks: Nonlinear-optic, ferroelectric, fluorescence sensing and photocatalytic properties. J. Mater. Chem. 2012, 22, 22603–22609.
Liu, D.S.; Sui, Y.; Chen, W.T.; Feng, P. Two new nonlinear optical and ferroelectric Zn(ll) compounds based on nicotinic acid and tetrazole derivative ligands. Cryst. Growth Des. 2015, 15, 4020–4025.
Hua, J.A.; Zhao, Y.; Zhao, D.; Kang, Y.S.; Chen, K.; Sun, W.Y. Functional group effects on structure and topology of cadmium(II) frameworks with mixed organic ligands. RSC Adv. 2015, 5, 43268–43278.
Pan, L.; Liu, G.; Li, H.; Meng, S.; Han, L.; Shang, J.; Chen, B.; Platero-Prats, A.E.; Lu, W.; Zou, X.; et al. A Resistance-Switchable and Ferroelectric Metal-Organic Framework. J. Am. Chem. Soc. 2014, 136, 17477–17483.
Fu, D.-W.; Zhang, W.; Xiong, R.-G. The first metal-organic framework (MOF) Imazethapyr and its SHG, piezoelectric and dielectric properties. Dalton Trans. 2008, 3946–3948.
Knebel, A.; Geppert, B.; Volgmann, K.; Kolokolov, D.I.; Stepanov, A.G.; Twiefel, J.; Heitjans, P.; Volkmer, D.; Caro, J. Defibrillation of soft porous metal-organic Frameworks with electric fields. Science 2017, 358, 347–351.
Sun, Y.; Hu, Z.; Zhao, D.; Zeng, K. Probing nanoscale functionalities of metal-organic framework nanocrystals. Nanoscale 2017, 9, 12163–12169.
Sun, Y.; Gao, J.; Cheng, Y.; Zhang, Y.-W.; Zeng, K. Design of the Hybrid Metal-Organic Frameworks (MOFs) as Potential Supramolecular Piezo/Ferro-Electrics. J. Phys. Chem. C 2019, 123, 3122–3129.
Lu, Y.; Young, D.J. Coordination polymers for n-type thermoelectric applications. Dalton Trans. 2020, 49, 7644–7657.
Ryder, M.R.; Donà, L.; Vitillo, J.G.; Civalleri, B. Understanding and controlling the dielectric response of metal-organic frameworks. ChemPlusChem 2018, 83, 308–316.
Warmbier, R.; Quandt, A.; Sefert, G. Dielectric properties of selected metal-organic frameworks. J. Phys. Chem. C 2014, 118, 11799–11805.
Redel, E.; Wang, Z.; Walheim, S.; Liu, J.; Gliermann, H.; Wöll, C. On the dielectric and optical properties of surface-anchored metal-organic frameworks: A study on epitaxially grown thin films. Appl. Phys. Lett. 2013, 103, 091903.
Eslava, S.; Zhang, L.; Esconjauregui, S.; Yang, J.; Vanstreels, K.; Baklanov, M.R.; Saiz, E. Metal-organic framework ZIF-8 films as low-κ dielectrics in microelectronics. Chem. Mater. 2013, 25, 27–33.
Usman, M.; Lee, C.-H.; Hung, D.-S.; Lee, S.-F.; Wang, C.-C.; Luo, T.-T.; Zhao, L.; Wu, M.-K.; Lu, K.-L. Intrinsic low dielectric behavior of a highly thermally stable Sr-based metal-organic framework for interlayer dielectric materials. J. Mater. Chem. C 2014, 2, 3762–3768.
Mendiratta, S.; Usman, M.; Chang, C.-C.; Lee, Y.-C.; Chen, J.-W.; Wu, M.-K.; Lin, Y.-C.; Hsu, C.-P.; Lu, K.-L. Zn(II)-based metal-organic framework: An exceptionally thermally stable, guest-free low dielectric material. J. Mater. Chem. C 2017, 5, 1508–1513.
Usman, M.; Mendiratta, S.; Lu, K.-L. Metal-organic frameworks: New interlayer dielectric materials. ChemElectroChem 2015, 2, 786–788.
Xing, X.-S.; Fu, Z.-H.; Zhang, N.-N.; Yu, X.-Q.; Wang, M.-S.; Guo, G.-C. High proton conduction in an excellent water-stable gadolinium metal-organic framework. Chem. Commun. 2019, 55, 1241–1244.
Okawa, H.; Shigematsu, A.; Sadakiyo, M.; Miyagawa, T.; Yoneda, K.; Ohba, M.; Kitagawa, H. Oxalate-bridged bimetallic complexes {NH(prol)3}[MCr(ox)3] (M = MnII, FeII, CoII.; NH(prol)3+ = tri(3-hydroxypropyl)ammonium) exhibiting coexistent ferromagnetism and proton conduction. J. Am. Chem. Soc. 2009, 131, 13516–13522.
Feng, L.; Wang, H.-S.; Xu, H.-L.; Huang, W.-T.; Zeng, T.-Y.; Cheng, Q.-R.; Pan, Z.-Q.; Zhou, H. A water stable layered Tb(III) polycarboxylate with a proton conductivity over 10−2 Scm−1 in a wide temperature range. Chem. Commun. 2019, 55, 1762–1765.
Bera, S.P.; Mondal, A.; Konar, S. Lanthanide based layer type two dimensional coordination polymers featuring slow magnetic relaxation, magnetocaloric effect and proton conductivity. Chem. Asian J. 2019, 14, 3702–3711.
Tang, Q.; Yang, Y.-L.; Zhang, N.; Liu, Z.; Zhang, S.-H.; Tang, F.-S.; Hu, J.-Y.; Zheng, Y.-Z.; Liang, F.-P. A multifunctional lanthanide carbonate cluster based metal-organic framework exhibits high proton transport and magnetic exchange change. Inorg. Chem. 2018, 57, 9020–9027.

© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.

Upload a video for this entry

Information

Subjects: Chemistry, Inorganic & Nuclear

Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :

Catherine Raptopoulou

View Times: 2.0K

Update Date: 13 Jan 2021

Table of Contents

Video Upload Options

Confirm