Search results for "stacking"

showing 10 items of 215 documents

On the staking of miniaturized air-breathing microbial fuel cells

2018

Abstract This work focuses on the scale-up of the MFCs by miniaturization and multiplication strategy. Performances of five stacks containing 1, 2, 5, 8 and 16 MFCs were compared. Each stack was evaluated under individual, parallel and series electrical connection as well as for cascade or individual hydraulic connection. Cascade feeding mode with a tank per stack favours the COD removal when the number of MFCs in the stack increases. However, despite operating without COD limitations, the energy production was disadvantaged. By changing the feeding system of a tank per stack into an individual tank per MFC, the performance of the whole stack enhances considerably. Stacking in series can in…

Microbial fuel cellMaterials scienceMicrobial fuel cellCombustiblesStackingStack02 engineering and technology010501 environmental sciencesManagement Monitoring Policy and Law01 natural sciencesStack (abstract data type)MiniaturizationMultiplicationProcess engineering0105 earth and related environmental sciencesMiniaturizationbusiness.industryMechanical EngineeringBuilding and Construction021001 nanoscience & nanotechnologyElectrical connectionPower (physics)ElectroquímicaGeneral EnergyCascadeCascade0210 nano-technologybusinessVoltage
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Diastereoselective formation of homochiral flexible perylene bisimide cyclophanes and their hybrids with fullerenes†‡

2021

Cyclophanes of different ring sizes featuring perylene-3,4:9,10-tetracarboxylic acid bisimide (PBI) linked by flexible malonates were designed, synthesized, and investigated with respect to their structural, chemical and photo-physical properties. It is predominantly the number of PBIs and their geometric arrangement, which influence dramatically their properties. For example, two-PBI containing cyclophanes reveal physico-chemical characteristics that are governed by strong co-facial π–π interactions. This is in stark contrast to cyclophanes with either three or four PBIs. Key to co-facial π–π stackings are the flexible malonate linkers, which, in turn, set up the ways and means for diaster…

Fullerene010405 organic chemistryStackingDiastereomerGeneral Chemistry010402 general chemistryRing (chemistry)01 natural sciences0104 chemical sciencesCrystallographychemistry.chemical_compoundChemistrychemistryProton NMRSelectivityChirality (chemistry)PeryleneChemical Science
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Reconstructed bcc Co films on the surface

2007

Abstract Ultrathin epitaxial Co films on Cr ( 1 1 0 ) are examined by scanning tunneling microscopy and spectroscopy (STM and STS). At room temperature Co grows as pseudomorphic bcc layers for the first two monolayers and forms close-packed Co layers with stacking faults for thicker coverages. A periodic lattice distortion appears in two equivalent (3 × 1) reconstruction domains in combination with a regular lattice of dislocation lines oriented along the in-plane close-packed row directions bcc [ 1 1 ¯ 1 ] and bcc [ 1 ¯ 1 1 ] . The reconstruction and the occurrence of dislocation lines are caused by the epitaxial strain. The local density-of-states function is mapped by scanning tunneling …

Materials scienceCondensed matter physicsScanning tunneling spectroscopyStackingchemistry.chemical_elementSurfaces and InterfacesTungstenCondensed Matter PhysicsEpitaxySurfaces Coatings and Filmslaw.inventionCrystallographychemistrylawMonolayerMaterials ChemistryScanning tunneling microscopeDislocationSpectroscopySurface Science
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Cobalt Metal-Organic Framework Based on Layered Double Nanosheets for Enhanced Electrocatalytic Water Oxidation in Neutral Media

2020

A new cobalt metal-organic framework (2D-Co-MOF) based on well-defined layered double cores that are strongly connected by intermolecular bonds has been developed. Its 3D structure is held together by π-π stacking interactions between the labile pyridine ligands of the nanosheets. In aqueous solution, the axial pyridine ligands are exchanged by water molecules, producing a delamination of the material, where the individual double nanosheets preserve their structure. The original 3D layered structure can be restored by a solvothermal process with pyridine, so that the material shows a "memory effect"during the delamination-pillarization process. Electrochemical activation of a 2D-Co-MOF@Nafi…

Aqueous solutionOxygen evolutionStackingIonic bondingchemistry.chemical_elementGeneral ChemistryCobaltQuímicaOverpotential010402 general chemistryElectrochemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundColloid and Surface ChemistryQUIMICA ORGANICAchemistryChemical engineeringPyridineQUIMICA ANALITICACobalt
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The Use of Polyoxometalates in the Design of Layer‐Like Hybrid Salts Containing Cationic Mn 4 Single‐Molecule Magnets

2013

Herein, we describe the combination of polyoxometalates (POMs) with a polynuclear metallic cluster Mn4 {Mn4 = [Mn4(OAc)2(pdmH)6]2+, (pdmH = deprotonated pyridine-2,6-dimethanol; C7H8NO2)} for the construction of ionic crystals with layered architectures. Choosing a POM with the appropriate charge and size not only allows for the fine tuning of the stacking periodicity, but it also allows modifying the in-plane packing motif and density of the cationic metallic clusters. The isolation of differently layered hybrid crystals with the same Mn4 single-molecule-magnet (SMM) system allowed for the direct comparison of the magnetic properties of such materials. The variation of the slow relaxation …

Spin statesChemistryInorganic chemistryRelaxation (NMR)StackingCationic polymerizationInorganic ChemistryMetalCrystallographyvisual_artvisual_art.visual_art_mediumCluster (physics)MoleculeHybrid materialEuropean Journal of Inorganic Chemistry
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7-Amino-2-methylsulfanyl-1,2,4-triazolo[1,5-a]pyrimidine-6-carboxylic acid as the dimethylformamide and water monosolvates at 293 K.

2010

The molecular structure of 7-amino-2-methylsulfanyl-1,2,4-triazolo[1,5-a]pyrimidine-6-carboxylic acid is reported in two crystal environments, viz. as the dimethylformamide (DMF) monosolvate, C(7)H(7)N(5)O(2)S·C(3)H(7)NO, (I), and as the monohydrate, C(7)H(7)N(5)O(2)S·H(2)O, (II), both at 293 (2) K. The triazolo[1,5-a]pyrimidine molecule is of interest with respect to the possible biological activity of its coordination compounds. While the DMF solvate exhibits a layered structural arrangement through N...O hydrogen-bonding interactions, the monohydrate displays a network of intermolecular O...O and N...O hydrogen bonds assisted by cocrystallized water molecules and weak π-π stacking intera…

chemistry.chemical_classificationPyrimidineMolecular StructureHydrogen bondStereochemistryCarboxylic acidStackingCarboxylic AcidsWaterDimethylformamideHydrogen BondingGeneral MedicineCrystal structureCrystallography X-RayGeneral Biochemistry Genetics and Molecular BiologyCoordination complexchemistry.chemical_compoundCrystallographyPyrimidineschemistrytriazolo- [15-a]pyrimidineSettore CHIM/03 - Chimica Generale E InorganicaSolventsDimethylformamideMoleculeActa crystallographica. Section C, Crystal structure communications
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Competition of Dzyaloshinskii-Moriya and Higher-Order Exchange Interactions in Rh/Fe Atomic Bilayers on Ir(111)

2018

Using spin-polarized scanning tunneling microscopy and density functional theory we demonstrate the occurrence of a novel type of noncollinear spin structure in $\mathrm{Rh}/\mathrm{Fe}$ atomic bilayers on Ir(111). We find that higher-order exchange interactions depend sensitively on the stacking sequence. For fcc-$\mathrm{Rh}/\mathrm{Fe}/\mathrm{Ir}(111)$, frustrated exchange interactions are dominant and lead to the formation of a spin spiral ground state with a period of about 1.5 nm. For hcp-$\mathrm{Rh}/\mathrm{Fe}/\mathrm{Ir}(111)$, higher-order exchange interactions favor an up-up-down-down ($\ensuremath{\uparrow}\ensuremath{\uparrow}\ensuremath{\downarrow}\ensuremath{\downarrow}$) s…

Condensed Matter::Quantum GasesPhysicsCondensed matter physicsMagnetic momentStackingGeneral Physics and Astronomy02 engineering and technologySpin structureType (model theory)021001 nanoscience & nanotechnology01 natural scienceslaw.inventionlaw0103 physical sciencesPhysics::Atomic and Molecular ClustersCondensed Matter::Strongly Correlated ElectronsDensity functional theoryScanning tunneling microscope010306 general physics0210 nano-technologySpin (physics)Ground statePhysical Review Letters
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Structure of anisole derivatives by total neutron and X-ray scattering: Evidences of weak C–H⋯O and C–H⋯π interactions in the liquid state

2020

Abstract High resolution, total neutron and X-ray scattering data have been used in synergy with Molecular Dynamics simulations to access atomistic scale insight into the structure of anisole and 2,3,5-trimethylanisole, two aromatic compounds bearing an electron-donating methoxy group. A detailed description is provided for the main interactions occurring in these systems, including π-π stacking and weak hydrogen bonding correlations: C H⋯O and C H⋯π. The existence of preferential orientations of the first shell coordinating molecules and the specific nature of the interactions involving the π cloud and the polar methoxy group have been reported and discussed.

Materials scienceStacking02 engineering and technologyNeutron scattering010402 general chemistry01 natural sciencesAnisole Hydrogen bonding Solvation π-πstocking Neutron scattering X-ray scattering Molecular dynamicchemistry.chemical_compoundMolecular dynamicsMaterials ChemistryMoleculePhysical and Theoretical ChemistrySpectroscopyScatteringHydrogen bondSolvation021001 nanoscience & nanotechnologyCondensed Matter PhysicsAnisoleAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallographychemistryAnisole Aromatic C–H/O C–H/π Hydrogen bonding Molecular dynamics Neutron scattering Solvation X-ray scattering π-π stacking0210 nano-technology
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Structure determination of three polymorphs of xylazine from laboratory powder diffraction data

2014

The crystal structures of three xylazine hydrochloride [N-(2,6-dimethylphenyl)-5,6-dihydro-4H-1,3-thiaz-2-amine hydrochloride] polymorphsA,ZandXhave been solved from powder diffraction data and refined using Rietveld refinement. Data were obtained with Cu Kα radiation. All polymorphs were found to have structures withZ′ = 1 andZ= 4. All the structures determined contained strong hydrogen bonds between the amino groups and chloride anions. The crystal structures of formsAandXfeatured π–π stacking interactions.

Rietveld refinementHydrogen bondChemistryHydrochlorideMetals and AlloysStackingCrystal structureChlorideAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic Materialschemistry.chemical_compoundCrystallographyPolymorphism (materials science)Materials ChemistrymedicinePowder diffractionmedicine.drugActa Crystallographica Section B Structural Science, Crystal Engineering and Materials
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Fluorine Scan of Inhibitors of the Cysteine Protease Human Cathepsin L: Dipolar and Quadrupolar Effects in the π-Stacking of Fluorinated Phenyl Rings…

2016

The π-stacking of fluorinated benzene rings on protein backbone amide groups was investigated, using a dual approach comprising enzyme-ligand binding studies complemented by high-level quantum chemical calculations. In the experimental study, the phenyl substituent of triazine nitrile inhibitors of human cathepsin L (hCatL), which stacks onto the peptide amide bond Gly67-Gly68 at the entrance of the S3 pocket, was systematically fluorinated, and differences in inhibitory potency were measured in a fluorimetric assay. Binding affinity is influenced by lipophilicity (clog P), the dipole and quadrupole moments of the fluorinated rings, but also by additional interactions of the introduced fluo…

HalogenationNitrileStereochemistryCathepsin LStackingSubstituentchemistry.chemical_elementPeptideCysteine Proteinase InhibitorsMolecular Dynamics SimulationLigands010402 general chemistry01 natural sciencesBiochemistrychemistry.chemical_compoundAmideDrug DiscoveryHumansPeptide bondFluorometryGeneral Pharmacology Toxicology and PharmaceuticsTriazinePharmacologychemistry.chemical_classificationBinding SitesTriazines010405 organic chemistryOrganic ChemistryFluorineAmidesProtein Structure Tertiary0104 chemical sciencesKineticschemistryFluorineQuantum TheoryMolecular MedicineHydrophobic and Hydrophilic InteractionsChemMedChem
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