Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Organically pillared layer framework of [Eu(NH₂-BDC)(ox)(H₃O)].

ABSTRACT: The non-porous three-dimensional structure of poly[(μ₅-2-amino-benzene-1,4-di-carboxyl-ato)(μ₆-oxalato)(oxomium)europium(III)], [Eu(C₈H₅NO₄)(C₂O₄)(H₃O)] _n or [Eu^III(NH₂-BDC)(ox)(H₃O)] _n (NH₂-BDC^2- = 2-amino-terephthalate and ox^2- = oxalate) is constructed from two-dimensional layers of Eu^III-carboxyl-ate-oxalate, which are connected by NH₂-BDC^2- pillars. The basic structural unit of the layer is an edge-sharing dimer of TPRS-{Eu^IIIO₉}, which is assembled through the ox^2- moiety. The intra-layer void is partially occupied by TPR-{Eu^IIIO₆} motifs. Weak C-H⋯O and strong, classical intra-molecular N-H⋯O and inter-molecular O-H⋯O hydrogen-bonding inter-actions, as well as weak π-π stacking inter-actions, affix the organic pillars within the framework. The two-dimensional layer can be simplified to a uninodal 4-connected sql/Shubnikov tetra-gonal plane net with point symbol {4⁴.6²}.

SUBMITTER: Thammakan S

PROVIDER: S-EPMC6895952 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Organically pillared layer framework of [Eu(NH2-BDC)(ox)(H3O)].

Thammakan Supaphorn S Panyarat Kitt K Rujiwatra Apinpus A

Acta crystallographica. Section E, Crystallographic communications 20191108 Pt 12

The non-porous three-dimensional structure of poly[(μ5-2-amino-benzene-1,4-di-carboxyl-ato)(μ6-oxalato)(oxomium)europium(III)], [Eu(C8H5NO4)(C2O4)(H3O)] n or [EuIII(NH2-BDC)(ox)(H3O)] n (NH2-BDC2- = 2-amino-terephthalate and ox2- = oxalate) is constructed from two-dimensional layers of EuIII-carbox ...[more]

PMID: 31871740

Similar Datasets

Inter-layer magnetic tuning by gas adsorption in π-stacked pillared-layer framework magnets.

Project description:Magnetism of layered magnets depends on the inter-layer through-space magnetic interactions (J NNNI). Using guest sorption to address inter-layer pores in bulk-layered magnets is an efficient approach to magnetism control because the guest-delicate inter-layer distance (l trans) is a variable parameter for modulating J NNNI. Herein, we demonstrated magnetic changes induced by the adsorption of CO2, N2, and O2 gases in various isostructural layered magnets with a π-stacked pillared-layer framework, , (M = Co, 1, Fe, 2, Cr, 3; Cp* = η5-C5Me5; 2,3,5,6-F4PhCO2 - = 2,3,5,6-tetrafluorobenzoate; TCNQ = 7,7,8,8-tetracyano-p-quinodimethane). Each compound had almost identical adsorption capability for the three types of gases; only CO2 adsorption was found to have a gated profile. A breathing-like structural modulation involving the extension of l trans occurred after the insertion of gases into the isolated pores between the [Ru2]2-TCNQ ferrimagnetic layers, which is more significant for CO2 than for O2 and N2, due to the CO2-gated transition. While adsorbent 1 with M = Co (S = 0) was an antiferromagnet with T N = 75 K, 1⊃CO2 was a ferrimagnet with T C = 76 K, whereas 1⊃N2 and 1⊃O2 were antiferromagnets with T N = 68 K. The guest-insertion effect was similarly confirmed in 2 and 3, and was characteristically dependent on the type of sandwiched spin in as M = Fe (S = 1/2) and Cr (S = 3/2), respectively. This study reveals that common gases such as CO2, O2, and N2 can serve as crucial triggers for the change in magnetism as a function of variable parameter l trans.

| S-EPMC9890543 | biostudies-literature

Non-Calcined Layer-Pillared Mn0.5Zn0.5 Bimetallic-Organic Framework as a Promising Electrocatalyst for Oxygen Evolution Reaction.

Project description:Electrocatalytic generation of oxygen is of great significance for sustainable, clean, and efficient energy production. Multiple electron transfer in oxygen evolution reaction (OER) and its slow kinetics represent a serious hedge for efficient water splitting, requiring the design and development of advanced electrocatalysts with porous structures, high surface areas, abundant electroactive sites, and low overpotentials. These requisites are common for metal-organic frameworks (MOFs) and derived materials that are promising electrocatalysts for OER. The present work reports on the synthesis and full characterization of a heteroleptic 3D MOF, [Zn2(μ4-odba)2(μ-bpdh)]n·nDMF (Zn-MUM-1), assembled from 4,4'-oxydibenzoic acid and 2,5-bis(4-pyridyl)-3,4-diaza-2,4-hexadiene (bpdh). Besides, a series of heterometallic MnZn-MUM-1 frameworks (abbreviated as Mn0.5Zn0.5-MUM-1, Mn0.66Zn0.33-MUM-1, and Mn0.33Zn0.66-MUM-1) was also prepared, characterized, and used for the fabrication of working electrodes based on Ni foam (NF), followed by their exploration in OER. These noble-metal-free and robust electrocatalysts are stable and do not require pyrolysis or calcination while exhibiting better electrocatalytic performance than the parent Zn-MUM-1/NF electrode. The experimental results show that the Mn0.5Zn0.5-MUM-1/NF electrocatalyst features the best OER activity with a low overpotential (253 mV at 10 mA cm-2) and Tafel slope (73 mV dec-1) as well as significant stability after 72 h or 6000 cycles. These excellent results are explained by a synergic effect of two different metals present in the Mn-Zn MOF as well as improved charge and ion transfer, conductivity, and stability characteristics. The present study thus widens the application of heterometallic MOFs as prospective and highly efficient electrocatalysts for OER.

| S-EPMC9775468 | biostudies-literature

Layer-by-layer self-assembly of pillared two-dimensional multilayers.

Project description:We report Layer-by-Layer (LbL) self-assembly of pillared two-dimensional (2D) multilayers, from water, onto a wide range of substrates. This LbL method uses a small molecule, tris(2-aminoethyl) amine (TAEA), and a colloidal dispersion of Ti3C2Tx MXene to LbL self-assemble (MXene/TAEA)n multilayers, where n denotes the number of bilayers. Assembly with TAEA results in highly ordered (MXene/TAEA)n multilayers where the TAEA expands the interlayer spacing of MXene flakes by only ~ 1 Å and reinforces the interconnection between them. The TAEA-pillared MXene multilayers show the highest electronic conductivity of 7.3 × 104 S m-1 compared with all reported MXene multilayers fabricated by LbL technique. The (MXene/TAEA)n multilayers could be used as electrodes for flexible all-solid-state supercapacitors delivering a high volumetric capacitance of 583 F cm-3 and high energy and power densities of 3.0 Wh L-1 and 4400 W L-1, respectively. This strategy enables large-scale fabrication of highly conductive pillared MXene multilayers, and potentially fabrication of other 2D heterostructures.

| S-EPMC6560128 | biostudies-literature

The role of surface deformation on responsivity of the pillared layer metal-organic framework DUT-8(Ni).

Project description:A unique feature of flexible metal-organic frameworks (MOFs) is their ability to respond dynamically towards molecular stimuli by structural transitions, resulting in pore-opening and closing processes. One of the most intriguing modes is the "gating", where the material transforms from the dense to the porous state. The conditions required for the solid phase structural transition are controlled by the kinetic barriers, including nucleation of the new phase commencing on the crystallite's outer surface. Thus, surface deformation may influence the nucleation, enabling deliberate tailoring of the responsivity. In the present contribution, we investigate how chemical surface treatments (surface deformation) affect the gate opening characteristics of a typical representative of gate pressure MOFs, DUT-8(Ni) ([Ni2(ndc)2(dabco)] n , ndc = 2,6-naphthalenedicarboxylate, dabco = 1,4-diazabicyclo[2.2.2]octane). A combination of various complementary advanced characterization techniques, such as NMR, nanoFTIR, terahertz, in situ XPS, in situ EPR spectroscopies, and inverse gas chromatography, are applied to unravel the changes in surface energy and mechanism of surface deformation.

| S-EPMC11912024 | biostudies-literature

Simultaneous adsorption of SO2 and CO2 in an Ni(bdc)(ted)0.5 metal-organic framework.

Project description:The metal-organic framework Ni(bdc)(ted)0.5 is a promising material for simultaneous capture of harmful gases such as SO2 and CO2. We found that SO2 performs much better than CO2 during adsorption, and the lack of physical insight was clarified through detailed analyses of the electronic structures obtained from density functional theory calculations. Our results showed that strong interactions of the d band of Ni atoms with the valence states (2n, 3n, and 4n) of SO2 but almost not with those of CO2 are the main reasons. Our finding is useful for the rational design of new metal-organic frameworks with suitable interactions for the simultaneous capture of not only SO2 and CO2 but also other gases.

| S-EPMC9091012 | biostudies-literature

Impact of Crystal Size and Morphology on Switchability Characteristics in Pillared-Layer Metal-Organic Framework DUT-8(Ni).

Project description:Variation of the crystallite size in flexible porous coordination polymers can significantly influence or even drastically change the flexibility characteristics. The impact of crystal morphology, however, on the dynamic properties of flexible metal-organic frameworks (MOFs) is poorly investigated so far. In the present work, we systematically modulated the particle size of a model gate pressure MOF (DUT-8(Ni), Ni2(2,6-ndc)2(dabco), 2,6-ndc-2,6-naphthalenedicarboxylate, dabco-1,4-diazabicyclo[2.2.2]octane) and investigated the influence of the aspect ratio, length, and width of anisotropically shaped crystals on the gate opening characteristics. DUT-8 is a member of the pillared-layer MOF family, showing reversible structural transition, i.e., upon nitrogen physisorption at 77 K. The framework crystalizes as rod-like shaped crystals in conventional synthesis. To understand which particular crystal surfaces dominate the phenomena observed, crystals similar in size and differing in morphology were involved in a systematic study. The analysis of the data shows that the width of the rods (corresponding to the crystallographic directions along the layer) represents a critical parameter governing the dynamic properties upon adsorption of nitrogen at 77 K. This observation is related to the anisotropy of the channel-like pore system and the nucleation mechanism of the solid-solid phase transition triggered by gas adsorption.

| S-EPMC8155289 | biostudies-literature

High-Quality Thin Films of UiO-66-NH2 by Coordination Modulated Layer-by-Layer Liquid Phase Epitaxy.

Project description:We report the fabrication of macroscopically and microscopically homogeneous, crack-free metal-organic framework (MOF) UiO-66-NH2 (UiO: Universitetet i Oslo; [Zr6 O4 (OH)4 (bdc-NH2 )6 ]; bdc-NH2 2- : 2-amino-1,4-benzene dicarboxylate) thin films on silicon oxide surfaces. A DMF-free, low-temperature coordination modulated (CM), layer-by-layer liquid phase epitaxy (LPE) using the controlled secondary building block approach (CSA). Efficient substrate activation was determined as a key factor to obtain dense and smooth coatings by comparing UiO-66-NH2 thin films grown on ozone and piranha acid-activated substrates. Films of 2.60 μm thickness with a minimal surface roughness of 2 nm and a high sorption capacity of 3.53 mmol g-1 MeOH (at 25 °C) were typically obtained in an 80-cycle experiment at mild conditions (70 °C, ambient pressure).

| S-EPMC8251636 | biostudies-literature

Ratio fluorescence detection of tetracycline by a Eu3+/NH2-MIL-53(Al) composite.

Project description:Tetracycline detection has been a great concern because of its overuse and difficulty in degrading. Here, a detection method with ratio fluorescence was developed by synthesizing Eu3+ doped nanocomposites with NH2-MIL-53(Al) nanosheets. After adding tetracycline, the fluorescence intensity at 616 nm characteristic emission peak of Eu3+ was sensitized by the antenna effect generated from coordinating Eu3+ with tetracycline, but the fluorescence of NH2-MIL-53(Al) at 433 nm was quenched by the fluorescence resonance energy transfer between the Eu3+-tetracycline composition and NH2-MIL-53(Al). Therefore, the efficient detection of tetracycline was achieved based on this change of ratio fluorescence signal. The experimental results show that Eu3+/NH2-MIL-53(Al) has excellent selectivity, a wider linear range and a lower detection limit for detecting tetracycline. This method can afford favorable ideas for developing advanced chemical and biological sensors.

| S-EPMC8693705 | biostudies-literature

Isomerism in double-pillared-layer coordination polymers - structures and photoreactivity.

Project description:The existence of isomerism in coordination polymeric structures offers opportunities to understand structure-function relationships. Herein the serendipitous isolation is reported of two isomeric double-pillared-layer coordination polymeric structures arising from two different types of carboxyl-ate bonding of benzene-1,4-di-carboxyl-ate ligands to zinc(II), which constitutes a new type of structural isomerism. The different bonding modes not only alter the shape and size of the pores, but also the nature of interpenetration and photoreactivity. Although two trans,cis,trans-bpeb ligands with conjugated olefin bonds are aligned in close proximity in both of the structures, one isomer undergoes a double [2 + 2] cyclo-addition reaction and the second isomer only offers an incomplete single cyclo-addition product. This work demonstrates how small changes in the structural connectivity can have an impact on the overall structural, physical and chemical properties of such materials.

| S-EPMC5947723 | biostudies-literature

All-in-One Electric Double Layer Supercapacitors Based on CH3NH3PbI3 Perovskite Electrodes.

Project description:Supercapacitors (SCs) are widely used energy storage devices in various applications that require instantaneous power supply and fast response times; however, the challenge for achieving high performance demands the continuous development and tailoring of electrode materials. Organic-inorganic halide perovskites (OIHPs) have recently received significant attention in electrochemical energy storage and conversion applications due to their unique properties including high charge carrier mobility, high mixed (electronic-ionic) conductivity, and presence of large oxygen vacancies. This study presents the fabrication and use of OIHPs based on methyl-ammonium lead iodide (CH3NH3PbI3) and its Co2+- and Bi3+-substituted derivatives (CH3NH3Pb1-x Co x I3 and CH3NH3Pb1-x Bi x I3, respectively, where x = 0.1) as electrodes for SCs. SC devices were constructed symmetrically by sandwiching the synthesized electrode materials in a quasi-solid-state electrolyte between two TiO2-coated FTO glasses. We discussed the optimization parameters (i.e., A-site doping, B-site doping, and controlling the stoichiometry of the anion and cation) to improve the electrochemical performance of the fabricated SCs. Furthermore, the effects of substitution ions (Co2+ and Bi3+) on the charge-discharge performance, energy and power density, defects, crystallinity, and microstructure were demonstrated. Electrochemical performances of the electrodes were analyzed by using CV, EIS, and GCPL techniques. The highest power density of 934.6 W/kg was obtained for Bi-substituted perovskite electrodes. Fabricated SC devices show good cyclability with 97.2, 96.3, and 86.6% retention of the initial capacitances after 50 cycles for pure, Co2+-substituted, and Bi3+-substituted perovskite electrodes, respectively.

| S-EPMC9774324 | biostudies-literature