Search results for "FRAM"

showing 10 items of 2142 documents

Bicyclo[2.2.2]octane-1,4-dicarboxylic acid: towards transparent metal–organic frameworks

2017

The preparation of transparent porous materials can offer a different access towards the study of molecules under solid confined space. Metal-organic frameworks represent a unique opportunity due to their tunable pore size, however aromatic linkers present strong absorption and reduce the transparency. Herein, we report the first example of a MOF with bicyclic organic dicarboxylic linkers and its use as a solid solvent.

chemistry.chemical_classificationMaterials scienceBicyclic molecule02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistry0104 chemical sciencesInorganic ChemistrySolventchemistry.chemical_compoundDicarboxylic acidchemistryOrganic chemistryMoleculeMetal-organic frameworkAbsorption (chemistry)0210 nano-technologyPorous mediumOctaneDalton Transactions
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A pea nuclear protein that is induced by dehydration belongs to the vicilin superfamily

2000

The purification to homogeneity of p16, a protein with an electrophoretic mobility compatible with an apparent molecular mass of 16 kDa, from nuclei of ungerminated pea embryonic axes is described. A cDNA clone of its gene, which was designated psp54, was also isolated. The psp54 cDNA contains an open reading frame coding for a 54.4-kDa polypeptide (p54). p16 corresponds to the C-terminal third of p54, although the mechanisms by which the primary polypeptide could be processed are not yet known. The sequence of p54 is 60% identical with that of the precursor of a sucrose-binding soybean protein, and, to a lesser extent (31-34%), it shares homology with some storage proteins. p16 is also 30%…

chemistry.chemical_classificationOpen reading frameBiochemistrychemistryComplementary DNAGene expressionVicilinStorage proteinNuclear proteinBiologyBiochemistryGenePeptide sequenceEuropean Journal of Biochemistry
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Enhanced Sieving of C2‐Hydrocarbon from Methane by Fluoro‐Functionalization of In‐MOF with Robust Stability

2021

Developing efficient adsorbent materials is crucial for adsorption and separation to realize the purification of energy source and raw chemicals. Here, we report a novel and robust 3D In-based MOF built up with fluorine-functionalized ligands, QMOF-2F, with improved separation properties of C2-light hydrocarbons over methane at room temperature respect isoreticular non-fluorinated MOF. QMOF-2F shows a remarkable chemical stability in different solvents, including water, and pH (2-12). DFT calculations support the key role of fluorine-functionalization on the improved performance of QMOF-2F.

chemistry.chemical_classificationOrganic ChemistryGeneral ChemistryBiochemistryMethaneImproved performancechemistry.chemical_compoundAdsorptionHydrocarbonchemistryChemical engineeringSurface modificationChemical stabilityMetal-organic frameworkEnergy sourceChemistry – An Asian Journal
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Postsynthetic Approach for the Rational Design of Chiral Ferroelectric Metal–Organic Frameworks

2017

International audience; Ferroelectrics (FEs) are materials of paramount importance with a wide diversity of applications. Herein, we propose a postsynthetic methodology for the smart implementation of ferroelectricity in chiral metal−organic frameworks (MOFs): following a single-crystal to single-crystal cation metathesis, the Ca2+ counterions of a preformed chiral MOF of formula Ca6II{CuII24[(S,S)-hismox]12(OH2)3}·212H2O (1), where hismox is a chiral ligand derived from the natural amino acid l-histidine, are replaced by CH3NH3+. The resulting compound, (CH3NH3)12{CuII24[(S,S)-hismox]12(OH2)3}·178H2O (2), retains the polar space group of 1 and is ferroelectric below 260 K. These results op…

chemistry.chemical_classificationStereochemistryChiral ligandRational design02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyMetathesis01 natural sciencesBiochemistryFerroelectricityCatalysis0104 chemical sciencesCrystallographyColloid and Surface Chemistrychemistry[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Metal-organic frameworkCounterion0210 nano-technology
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The dcuD (former yhcL ) gene product of Escherichia coli as a member of the DcuC family of C4-dicarboxylate carriers: lack of evident expression

1999

The dcuD gene (formerly yhcL) of Escherichia coli shows significant sequence similarity only to the dcuC gene of E. coli, which encodes a C4-dicarboxylate carrier (DcuC) that functions during anaerobic growth. Inactivation of dcuD had no effect on the growth of E. coli under a large number of conditions and led to no detectable changes in phenotype. Translational dcuD'-'lacZ gene fusions were not significantly expressed in the presence of dicarboxylates or monocarboxylates under oxic or anoxic conditions. Other potential substrates such as amino sugar derivatives, amino acids, and alpha-aspartyl dipeptides also did not lead to expression of dcuD. Changes in medium composition, pH, ionic str…

chemistry.chemical_classificationbiologyHypothetical proteinGeneral Medicinebiology.organism_classificationmedicine.disease_causeBiochemistryMicrobiologyEnterobacteriaceaeAmino acidGene productOpen reading frameBiochemistrychemistryGene expressionGeneticsmedicineMolecular BiologyEscherichia coliGeneArchives of Microbiology
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Investigation of Charge-Transfer Interactions Induced by Encapsulating Fullerene in a Mesoporous Tetrathiafulvalene-Based Metal-Organic Framework

2019

<p>The design of Metal-Organic Frameworks (MOFs) incorporating electroactive guest molecules in the pores has become a subject of great interest in order to install additional electrical functionalities within the framework while maintaining porosity. In this direction, understanding the charge-transfer (CT) process between the framework and the guest molecules is crucial towards the design of new electroactive MOFs. Herein, we present the encapsulation of fullerenes (C<sub>60</sub>) in a mesoporous tetrathiafulvalene(TTF)-based MOF. The CT process between the electron-acceptor C<sub>60 </sub>guest and the electron-donor TTF ligand is studied in detail by means…

chemistry.chemical_compoundMaterials scienceFullerenechemistryMoleculeMetal-organic frameworkNanotechnologySorptionDensity functional theoryMesoporous materialPorosityTetrathiafulvalene
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Metal-organic frameworks-based catalysts for biomass valorization

2020

Abstract The objective of this chapter is to review the most promising metal-organic framework (MOF) catalysts in biomass valorization processes in the bulk and fine chemical industries. Either bulk metal-organic frameworks, encapsulated catalytic species in MOFs, or MOF-derived catalysts are revised in terms of activity, selectivity, and stability for biomass valorization applications. The work revised here is focused on the transformation of lignocellulose biomass through purely chemical pathways. In the first part of the chapter, the few studies of cellulose hydrolysis into monosaccharides reported are commented, since this crucial first step in the valorization of hemicellulose is expec…

chemistry.chemical_compoundchemistryFuranfungiOrganic chemistryFine chemicalHemicelluloseMetal-organic frameworkAldol condensationFurfuralCatalysisFurfuryl alcohol
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Temperature-Induced Structural Transitions in the Gallium-Based MIL-53 Metal–Organic Framework

2013

We report a structural and thermodynamic investigation of the phase behavior of Ga(OH,F)-MIL-53, a gallium-based metal–organic framework (MOF) having the MIL-53 topology containing 0.7 wt % fluorine bonded to the metal. Despite some small structural differences, especially for the hydrated form, the overall physical chemistry behavior of Ga(OH,F)-MIL-53 is very similar to standard fluorine free Ga-MIL-53 material. A combination of in situ X-ray diffraction, in situ Fourier transform infrared spectroscopy, differential scanning calorimetry, and heat capacity measurements allowed us to establish that Ga(OH,F)-MIL-53 under vacuum (i.e., the empty material) exhibits two stable phases: a nonporo…

chemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesHeat capacityMetalDifferential scanning calorimetryPhase (matter)[CHIM] Chemical Sciences[CHIM]Chemical SciencesPhysical and Theoretical ChemistryGalliumFourier transform infrared spectroscopyComputingMilieux_MISCELLANEOUS[CHIM.MATE] Chemical Sciences/Material chemistry[CHIM.MATE]Chemical Sciences/Material chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materials[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistryCrystallographyGeneral Energychemistryvisual_artvisual_art.visual_art_mediumFluorinePhysical chemistryMetal-organic framework0210 nano-technology
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Selective Gold Recovery and Catalysis in a Highly Flexible Methionine-Decorated Metal–Organic Framework

2016

A novel chiral 3D bioMOF exhibiting functional channels with thio-alkyl chains derived from the natural amino acid l-methionine (1) has been rationally prepared. The well-known strong affinity of gold for sulfur derivatives, together with the extremely high flexibility of the thioether "arms" decorating the channels, account for a selective capture of gold(III) and gold(I) salts in the presence of other metal cations typically found in electronic wastes. The X-ray single-crystal structures of the different gold adsorbates Au(III)@1 and Au(I)@1 suggest that the selective metal capture occurs in a metal ion recognition process somehow mimicking what happens in biological systems and protein r…

chemistry.chemical_element02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciencesBiochemistrySulfurCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryThioetherchemistryvisual_artvisual_art.visual_art_mediumOrganic chemistryMetal-organic framework0210 nano-technologyHybrid materialHydroalkoxylationJournal of the American Chemical Society
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Bidirectional Chemo-Switching of Spin State in a Microporous Framework

2009

The ins and outs of spin: Using the microporous coordination polymer {Fe(pz)[Pt(CN)(4)]} (1, pz=pyrazine), incorporating spin-crossover subunits, two-directional magnetic chemo-switching is achieved at room temperature. In situ magnetic measurements following guest vapor injection show that most guest molecules transform 1 from the low-spin (LS) state to the high-spin (HS) state, whereas CS(2) uniquely causes the reverse HS-to-LS transition.

chemo-switchingSpin statesPyrazinemicroporous materialsCoordination polymerGeneral ChemistryMicroporous materialCatalysiscoordination polymerschemistry.chemical_compoundCrystallographyspin crossoverchemistrySpin crossoverMoleculeMetal-organic frameworkSpin (physics)metal-organic frameworksAngewandte Chemie International Edition
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