Zeolitic boron imidazolate frameworks with 4-connected octahedral metal centers

Solvent selection! The organically templated co-assembly between tetrahedral [B(imidazolate)(4) ](-) and [Co(ac)](+) units leads to two previously unknown zeolitic boron imidazolate frameworks with ACO and ABW topologies (denoted BIF-22 and BIF-23; e-urea=ethyleneurea), respectively. BIF-22 is chiral and shows interesting CO(2) selectivity over N(2) and CH(4) .     

Syntheses,Crystal Structures and Properties of Two New Zn Based Boron Imidazolate Frameworks

Two new boron imidazolate frameworks (BIFs),Zn_2[HBH(2-mim)_3]_2(1,2-PEA)_2(EG)_(2 )(BIF-120,EG=ethylene glycol) and Zn[BH(2-mim)_3](1,2-HPEA)(BIF-121),were successfully synthesized by mixing the KBH(2-mim)_3 ligand and the semirigid aromatic dicarboxylate ligand 1,2-benzenediacetic acid (1,2-H_2PEA) under solvothermal conditions.In this paper,the two samples were structurally characterized by single-crystal X-ray diffraction and tested by infrared spectroscopy (IR),UV-visible spectroscopy (UV-Vis),thermogravimetric analysis TGA and X-ray powder diffractions.In addition,the solid-state luminescent properties of these crystals were also investigated.     

Structure and charge control in metal-organic frameworks based on the tetrahedral ligand tetrakis(4-tetrazolylphenyl)methane

Use of the tetrahedral ligand tetrakis(4-tetrazolylphenyl)methane enabled isolation of two three-dimensional metal-organic frameworks featuring 4,6- and 4,8-connected nets related to the structures of garnet and fluorite with the formulae Mn(6)(ttpm)(3)5 DMF3 H(2)O (1) and Cu[(Cu(4)Cl)(ttpm)(2)](2)CuCl(2)5 DMF11 H(2)O (2) (H(4)ttpm=tetrakis(4-tetrazolylphenyl)methane). The fluorite-type solid 2 displays an unprecedented post-synthetic transformation in which the negative charge of the framework is reduced by extraction of copper(II) chloride. Desolvation of this compound generates Cu(4)(ttpm)(2)0.7 CuCl(2) (2 d), a microporous material exhibiting a high surface area and significant hydrogen uptake.     

A Novel 3D Metal Organic Framework Based on an Azolate Ligand

Metal organic frameworks（MOFs） have attracted much attention over the world during the last several decades[1-3].Constructed from metal ions and organic building units,MOFs have great properties in gas adsorption[4],catalysis[5],luminescence[6] and magnetism[7].By varying the metal salts and organic building units,numerous MOF structures with designed functionalities and expected properties can be obtained.Among them,zeolitic imidazolate frameworks（ZIFs） have been investigated greatly due to their high thermal and chemical stabilities and tunable porosities[8].ZIFs can be obtained with imidazolate compounds as organic building units,such as imidazole,benzimidazole and 2-methylimidazole[9].Zeolite structures are composed of tetrahedral Si（Al）O4 units,with Si-O-Si angle ca.145°.ZIFs possess imidazole,with M-IM-M（M-metal,IM=imidazole） angle close to 145°,resembling zeolite（Scheme 1）[10].     

A new approach towards tetrahedral imidazolate frameworks for high and selective CO2 uptake

Successful development of a new synthetic approach towards tetrahedral imidazolate frameworks (TIFs) via combining an auxiliary uninegative linker into the zinc-imidazolate tetrahedral assembly leads to new TIF materials (TIF-A1 to TIF-A3) with distinct structural topologies and high CO(2) uptake capacity.     

Synthesis, Structures, Fluorescence and Magnetism of Two Lanthanide Metal-organic Frameworks with CaF2 Topology Based on Silicon-centered Tetrahedral Ligand

Two 3D multifunctional lanthanide metal-organic frameworks(MOFs), Pr(HTCPS)(H₂O)·2DMF·C₂H₅OH· 5H₂O(JUC-93) and Pr₃(TCPS)₂(NO₃)(H₂O)₄(DMA)₂·2DMA·C₂H₅OH·3H₂O(JUC-94)[H₄TCPS=tetrakis(4-carboxyphenyl)- silane, DMF=N,N'-dimethylformamide, DMA=N,N'-dimethylacetamide and JUC=Jilin University China] were synthesized by the self-assembly of a rigid silicon-centered tetrahedral carboxylate ligand H₄TCPS and Pr(III) ions in different solvothermal reactions. X-Ray crystallography revealed that they exhibited a rare CaF₂ topology framework, constructed from the 4-connected tetrahedral TCPS unit with the 8-connected dinuclear praseodymium cluster unit and trinuclear praseodymium cluster unit, respectively. In addition, the luminescent and magnetic properties of the two compounds were investigated.     

A new enantiopure unsaturated dicarboxylate as a 4-connected unit in a flexible homochiral PtS-type framework

Metal cation mediated chiral ligand transformation of (S)-camphanic acid leads to a new enantiopure unsaturated dicarboxylate that links tetrahedral Zn(2+) sites into 3-D homochiral 4-connected PtS-type framework structures, Zn(tced) (1, H(2)tced=1,2,2-trimethyl-3-cyclopentene-1,3-dicarboxylic acid) and Zn(4)(tced)(4)(4,4'-bipy) (2, 4,4'-bipy=4,4'-bipyridine).     

Anchoring metal ions in amine-functionalized boron imidazolate framework for photocatalytic reduction of CO2

The photocatalytic reduction of CO₂ to energy-rich chemicals is highly appealing for alleviation of energy crisis and environment pollution.The introduction of different active sites is a key factor to determine the reaction activity and selectivity.Here,we demonstrate the metal ion-dependent performance for photocatalytic CO₂ reduction by anchoring transition metal ions (Co²⁺and Ni²⁺) in an amine-functionalized boron imidazolate framework （BIF-43）.As ...     

A cubic, 12-connected, microporous metal-organometallic phosphate framework sustained by truncated tetrahedral nodes

A rare example of a microporous metal-organic phosphate, [Co(12)(L)(6)(μ(3)-PO(4))(4)(μ(3)-F)(4)(μ-H(2)O)(6)][NO(3)](2) (1), is synthesized by the reaction of a [(η(5)-C(5)H(5))Fe(II)](+)-functionalized terephthalate ligand with Co(NO(3))(2)·6H(2)O and phosphate and fluoride ions generated from the in situ hydrolysis of hexafluorophosphate. 1 is a cubic, 12-connected, face-centered cubic framework sustained by the linear connection of unprecedented, dodecanuclear truncated tetrahedral coordination clusters.     

Syntheses, structures and physical properties of transition metal-organic frameworks assembled from trigonal heterofunctional ligands

Six novel metal-organic frameworks (MOFs), {Mn(bpydb)(bpyHdbH)}(n) (1) {[Co(2)(bpydb)(2)](H(2)O)(0.5)}(n) (2), {[Ni(0.5)(bpydbH)(H(2)O)](DMF)(2)}(n) (3), {[Cu(2)(bpydb)(2)](H(2)O)(0.5)}(n) (4), {Zn(bpyHdb)(2)}(n) (5) and {[Cd(0.5)(bpydb)(0.5)(DMF)](H(2)O)}(n) (6), were successfully synthesized by assembling transition metal salts with trigonal heterofunctional ligand 4,4'-(4,4'-bipyridine-2,6-diyl) dibenzoic acid (bpydbH(2)) under hydrothermal and/or solvothermal conditions. Compound 1 features a rare 4-fold interpenetrating (3,5)-connected framework with hms-type topology. Isostructural compounds 2 and 4, constructed by M(2)(COO)(4) secondary building units, exhibit a robust 3D framework with alb topological type in 2-fold interpenetrating mode. Compound 3 consists of 2D (4,4) networks, which are further assembled into the new topological framework with the symbol (5(3)·6(2)·8)(5(3)·6(3))(2) through O-HO interactions. Compound 5 manifests a novel 4-connected interpenetrating framework, constructed by 2D (4,4) layers and interbedded N-HO interactions. Non-interpenetrating honeycomb networks are observed in compound 6, and further packed into a 3D framework featuring 1D channels. The magnetic susceptibility of compound 2 indicates antiferromagnetic interactions between cobalt ions. The photoluminescent properties of 5 and 6 were investigated in the solid state at room temperature.     

Controllable preparation, network structures and properties of unusual metal-organic frameworks constructed from 4,4'-(hexafluoroisopropylidene)diphthalic acid and 4,4'-bipyridyl

Three novel 3D metal-organic frameworks of [Ni(2)(hfpdpt)(bpy)(2)(H(2)O)(2)](H(2)O)(8) (1), [Ni(3)(Hhfpdpt)(2)(bpy)(4)](H(2)O)(2) (2), and [Mn(2)(hfpdpt)(H(2)O)(2)] (3) have been synthesized by the hydrothermal reaction of Ni(II) or Mn(II) nitrate, 4,4'-(hexafluoroisopropylidene)diphthalic acid (H(4)hfpdpt), and 4,4'-bipyridyl (bpy). Complex 1 self-assembles into a 3D framework with unconventional 4-connected network topology, while 2 and 3 exhibit two kinds of unusual (4,8)-connected topological networks. Notably, in 1 and 2, the bpy coligand participates in the construction of their 3D frameworks, and the pH value also plays an important role to tune their space arrangements, while in 3, the bpy coligand is not involved in the final crystalline lattice. Furthermore, a detailed investigation on their magnetic and adsorptive properties is carried out.     

Homoleptic imidazolate frameworks [Sr(1-x)Eu(x)(Im)2]--hybrid materials with efficient and tuneable luminescence

Homoleptic frameworks of the formula [Sr(1-x)Eu(x)(Im)(2)] (1) (x = 0.01-1.0; Im(-) = imidazolate anion, C(3)H(3)N(2)(-)) are hybrid materials that exhibit an intensive green luminescence. Tuning of both emission wavelength and quantum yield is achieved by europium/strontium substitution so that a QE of 80% is reached at a Eu content of 5%. Even 100% pure europium imidazolate still shows 60% absolute quantum efficiency. Substitution of Sr/Eu shows that doping with metal cations can also be utilized for coordination compounds to optimize materials properties. The emission is finely tuneable in the region 495-508 nm via variation of the europium content. The series of frameworks [Sr(1-x)Eu(x)(Im)(2)] presents dense MOFs with the highest quantum yields reported for MOFs so far.     

A 3D canted antiferromagnetic porous metal-organic framework with anatase topology through assembly of an analogue of polyoxometalate

The unique porous metal-organic framework {KCo3(C6H4O7)(C6H5O7)(H2O)2.8H2O}8 (1), which exhibits an unprecedented infinite 3D (3,6)-connected decorated anatase net, has been obtained by hydrothermal reaction. Upon dehydration, the compound retains crystallinity and exhibits a type I N2 sorption isotherm, characteristic of a microporous solid with apparent Langmuir surface area 939 m2/g and pore volume 0.31 cm3/g. Magnetic measurements for both 1 and dehydrated 1 show the spin-canted antiferromagnetic state below 5 K and a magnetic hysteresis loop at 2 K. Thus, dehydrated 1 represents the first metal-organic framework for which microporosity and a spin-canted antiferromagnetic state coexist, which demonstrates that the self-assembly of organo-polymetal clusters and metal ions can provide a potential route to magnetic porous metal-organic frameworks.     

A 3,4-connected beryllium phosphite framework containing 24-ring channels with a very low density

A new three-dimensional open-framework beryllium phosphite with honeycomb-like channels has been prepared under solvothermal conditions. The alternation of a 24-ring window and a 30-ring window along its extra-large channel is unprecedented in open-framework materials. The compound has a very low density of 1.369 g cm(-3) by integrating an extra-large-pore, interrupted 3,4-connected framework and lightweight beryllium metal in its crystalline structure.     

Synthesis of an Interrupted AST‐Type Zeolitic Imidazolate Framework

Presented here is a new interrupted AST‐type zeolitic imidazolate framework, Zn₅(OH)(dmbim)₉(H₂O)? 4(DMF) ( 1 ) with cub and interrupted ast cages, which exhibits permanent porosity, high hydrophobicity and strong solid‐state photoluminescent properties. More importantly, structural ordered DMF molecules are firmly confined in the ‐ast cage by strong host‐guest interactions.     

Metal nuclearity modulated four-, six-, and eight-connected entangled frameworks based on mono-, bi-, and trimetallic cores as nodes

To investigate the relationship between network connectivity and metal nuclearity, we designed and synthesized a series of three-dimensional (3D) entangled coordination frameworks based on different metal cores, namely [Zn(2)(bdc)(2)(L)(2)]2H(2)O (1), [Zn(bdc)(L)(0.5)] (2), [Zn(oba)(L)(0.5)] (3) and [Cd(3)(bdc)(3)(L)(2)(H(2)O)(2)] (4) by self-assembly of d(10) metal salts with the flexible long-chain ligand 1,4-bis(1,2,4-triazol-1-yl)butane (L), and with the rigid and nonrigid aromatic dicarboxylate ligands 1,4-benzenedicarboxylate (bdc) and 4,4'-oxybis(benzoate) (oba). Compound 1 exhibits a threefold interpenetrated diamondoid array typically based on a tetrahedral second building unit (SBU) at a single Zn center. Compound 2 adopts a threefold interpenetrated alpha-polonium-type network that is built from bimetallic cores as six-connected vertices. The structure of 3 also consists of dinuclear units; it comprises a novel (3,4)-connected threefold interpenetrated net with complex (4610)(46(2)10(3)) topology when single zinc centers act as four-connected nodes (or the alpha-Po topology if dinuclear units are considered as six-connected nodes). Compound 4, derived from a crosslinked fivefold interpenetrated diamond-like substructure, is an unusual example of a self-penetrating coordination framework displaying an unprecedented eight-connected 4(20)6(8) topology with trinuclear cadmium clusters as eight-connected nodes which, to our knowledge, not only defines a new topology for eight-connected coordination networks, but also represents the highest connected topology presently known for self-penetrating systems. Detailed structural comparison of these complexes indicates that the increase in metal nuclearity induces the progressive increase in the connectivities of the ultimate nets: that is, the metal nuclearity plays a significant role in tuning the connectivity of a specific network. The thermal and luminescent properties of these compounds are discussed.     

Lanthanide-thiophene-2,5-dicarboxylate frameworks: ionothermal synthesis, helical structures, photoluminescent properties, and single-crystal-to-single-crystal guest exchange

Eight three-dimensional lanthanide-thiophene-2,5-dicarboxylate frameworks, [Ln(TDC)(2)]·(choline) (1-6; Ln = Gd, Nd, Eu, Er, Tb, Dy; TDC = thiophene-2,5-dicarboxylate), [Yb(TDC)(2)(e-urea)]·(choline)·H(2)O (7; e-urea = ethyleneurea), [Nd(2)(TDC)(3)(e-urea)(4)]·3(e-urea) (8) have been successfully prepared in deep eutectic solvents (choline chloride/e-urea), respectively. Compounds 1-7 are anionic frameworks with 8-connected bcu topology, while compound 8 features a neutral 6-connected rob-type framework with guest e-urea molecules. In these structures, lanthanide ions show dicapped trigonal prism, pentagonal bipyramid, and tricapped trigonal prism coordination configurations, respectively, and the TDC ligands exhibit different coordination modes. Versatile helical substructures are presented in these compounds. The photoluminescent properties of compounds 3 (Eu) and 8 (Nd) were studied. Moreover, compound 8 can perform single-crystal-to-single-crystal guest exchange. The ethanol-exchange mechanism of 8 can be ascribed to the kinetically controlled flexibility (KCF).     

Two mixed-valence copper(I,II) imidazolate coordination polymers: metal-valence tuning approach for new topological structures

A new metal-valence tuning synthetic approach has been utilized to generate two new mixed-valence Cu(I,II) coordination polymers Cu(2)(im)(3) and Cu(3)(im)(4)(Him = imidazole), which are an unprecedented uninodal 4-connected 4.8(5) topological net and a 4-connected (4,4) net, respectively.     

Microwave-assisted synthesis of a series of lanthanide metal-organic frameworks and gas sorption properties

A series of isostructural microporous lanthanide metal-organic frameworks (MOFs) formulated as [Ln(2)(TPO)(2)(HCOO)]·(Me(2)NH(2))·(DMF)(4)·(H(2)O)(6) {Ln = Y (1), Sm (2), Eu (3), Gd (4), Tb (5), Dy (6), Ho (7), Er (8), Tm (9), Yb (10), and Lu (11); H(3)TPO = tris-(4-carboxylphenyl)phosphineoxide; DMF = N,N-dimethylformamide} has been synthesized under microwave-assisted solvothermal reaction for 30 min. Alternatively, if a conventional solvothermal reaction is carried out under the same temperature, a much longer time (3 days) is needed for the same phase in similar yield. Structure analysis reveals that the framework is a 4,8-connected network with point symbol (4(10)·6(16)·8(2)) (4(5)·6)(2), which is the subnet of alb net. Thermal gravimetric analyses performed on as-synthesized MOFs reveal that the frameworks have high thermal stability. The luminescent properties of 2, 3, 5, and 6 were investigated and show characteristic emissions for Sm(III), Eu(III), Tb(III), and Dy(III) at room temperature, respectively. Gas sorption properties of 1 and 3 were studied by experimentally measuring nitrogen, argon, carbon dioxide, methane, and hydrogen sorption isotherms. The resulting materials show high and preferential CO(2) adsorption over N(2) gas at ambient temperature, indicating that the present materials can be applied in a CO(2) capture process.     

Highly porous 4,8-connected metal-organic frameworks: synthesis, characterization, and hydrogen uptake

A series of highly porous 4,8-connected isoreticular MOFs of the scu topology [Cu(4)(L(1))(H(2)O)(4)]·20DEF, [Cu(4)(L(2))(H(2)O)(4)]·16DMF·5H(2)O, and [Cu(4)(L(3))(H(2)O)(4)]·14DMF (L(1)-L(3) are (R)-1,1'-binaphthyl-derived octacarboxylate bridging ligands) were synthesized and characterized by single-crystal X-ray crystallography. Although the frameworks exhibit some distortion during the solvent removal process, the high-connectivity nature of the building blocks helps in stabilizing the frameworks, leading to high surface areas (S(BET) = 1189-2448 m(2)/g) and significant hydrogen uptake of up to 1.8 wt % (77 K, 1 atm).