Search results for "Note"

showing 10 items of 10709 documents

Morphology transitions in ZnO nanorods grown by MOCVD

2012

Morphology transitions (nanorods–nanowalls and nanorods–nanotubes-layer) were induced in the growth of ZnO nanostructures by metal organic chemical vapor deposition (MOCVD) on c-sapphire, using helium as carrier gas, and dimethylzinc–triethylamine and nitrous oxide as zinc and oxygen sources, respectively. A systematic study of the influence of the VI/II ratio and precursor flow-rates on the morphology of ZnO nanorod arrays has been carried out, taking advantage of the ability of MOCVD to individually control the precursor partial pressures. Growth mechanisms are discussed to understand the evolution of the nanostructures morphology for different growth conditions. In particular, the influe…

SupersaturationNanostructureMaterials scienceMorphology (linguistics)chemistry.chemical_elementNanotechnologyChemical vapor depositionPartial pressureZincCondensed Matter PhysicsInorganic ChemistryChemical engineeringchemistryMaterials ChemistryNanorodMetalorganic vapour phase epitaxyJournal of Crystal Growth
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Hierachical Ni@Fe2O3superparticles through epitaxial growth of γ-Fe2O3nanorods on: In situ formed Ni nanoplates

2016

One endeavour of nanochemistry is the bottom-up synthesis of functional mesoscale structures from basic building blocks. We report a one-pot wet chemical synthesis of Ni@γ-Fe2O3 superparticles containing Ni cores densely covered with highly oriented γ-Fe2O3 (maghemite) nanorods (NRs) by controlled reduction/decomposition of nickel acetate (Ni(ac)2) and Fe(CO)5. Automated diffraction tomography (ADT) of the Ni-Fe2O3 interface in combination with Mossbauer spectroscopy showed that selective and oriented growth of the γ-Fe2O3 nanorods on the Ni core is facilitated through the formation of a Fe0.05Ni0.95 alloy and the appearance of superstructure features that may reduce strain at the Ni-Fe2O3 …

SuperstructureMaterials scienceAlloyNanochemistryMaghemiteNanotechnology02 engineering and technologyengineering.material010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesMagnetizationChemical engineeringMössbauer spectroscopyengineeringSurface modificationGeneral Materials ScienceNanorodMaterials Science (all)0210 nano-technology
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Hierarchical Self-Assembly of Supramolecular Spintronic Modules into 1D- and 2D-Architectures with Emergence of Magnetic Properties

2004

Hierarchical self-assembly of complex supramolecular architectures allows for the emergence of novel properties at each level of complexity. The reaction of the ligand components A and B with Fe II cations generates the (2 K 2) grid-type functional building modules 1 and 2, presenting spin-tran- sition properties and preorganizing an array of coordination sites that sets the stage for a second assembly step. Indeed, binding of La III ions to 1 and of Ag I ions to 2 leads to a 1D columnar superstructure 3 and to a wall-like 2D layer 4, respectively, with concomitant modulation of the magnetic properties of 1 and 2. Thus, to each of the two levels of structural complexity generat- ed by the t…

SuperstructureSpintronicsLigandChemistryOrganic ChemistrySupramolecular chemistrySpin transitionNanotechnologyGeneral ChemistrySelf-assemblyLayer (object-oriented design)CatalysisStructural complexityChemistry - A European Journal
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Electrochemical Conversion of Dichloroacetic Acid to Chloroacetic Acid in Conventional Cell and in Two Microfluidic Reactors

2013

The electrochemical conversion of dichloroacetic acid to chloracetic acid is investigated in conventional cells and in microreactors. Two different microreactors are used: the first is a filter press cell equipped with PTFE micrometric spacers, easy to assemble and disassemble and available for a large variety of electrodes and solvents; the second is made using an adhesive spacer, micromilling and press and could easily be developed on an industrial scale. The electrochemical synthesis is performed successfully in the microreactors equipped with a graphite cathode under proper operative conditions. The performance of the process strongly depends on the nature of the cathode and, for micror…

Supporting electrolyteChloroacetic acidElectrochemical Microfluidic Reactors Chloroacetic AcidDichloroacetic acidNanotechnologyElectrochemistryCatalysisCathodelaw.inventionchemistry.chemical_compoundchemistrylawElectrodeElectrochemistryGraphiteMicroreactorChemElectroChem
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Electrochemical reduction of carbon dioxide to formic acid at a tin cathode in divided and undivided cells: effect of carbon dioxide pressure and oth…

2016

Abstract The reduction of carbon dioxide to formic acid at a tin cathode was studied in both divided and undivided cells. In the first stage of the study, the effect of some operating parameters, including the working potential and the nature of the supporting electrolyte and of the cathode, on both the cathodic reduction of CO2 and the anodic oxidation of formic acid was investigated in a divided cell. In a second stage, the reduction of carbon dioxide was performed in an undivided cell with the aim of studying the effect on the generation of formic acid of various operating parameters such as current density, cathode to anode area ratio, mixing rate and nature of the anode and of the supp…

Supporting electrolyteFormic acidGeneral Chemical EngineeringInorganic chemistrychemistry.chemical_elementFormic acid02 engineering and technology010402 general chemistryElectrochemistry01 natural sciencesCarbon dioxide conversionlaw.inventionchemistry.chemical_compoundlawElectrochemistryChemical Engineering (all)CO2 PressureTin cathodeElectrochemical reduction of carbon dioxideElectrochemical reduction021001 nanoscience & nanotechnologyCathode0104 chemical sciencesAnodeCarbon dioxidechemistryCarbon dioxide0210 nano-technologyTinElectrochimica Acta
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Supported iridium catalysts for the total oxidation of short chain alkanes and their mixtures: Influence of the support

2021

13 figures, 3 tables.-- Supplementary information available.-- © 2020. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/

SupportsGeneral Chemical EngineeringTotal oxidationchemistry.chemical_element02 engineering and technologyIridium oxide010402 general chemistryIridium01 natural sciencesIndustrial and Manufacturing EngineeringCatalysislaw.inventionsymbols.namesakeAdsorptionX-ray photoelectron spectroscopylawAlkanesEnvironmental ChemistryCalcinationIridiumVOCsGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryChemical engineeringsymbols0210 nano-technologyRaman spectroscopy
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Influence of theZ/EIsomerism on the Pathway Complexity of a Squaramide‐Based Macrocycle

2020

The rising interest on pathway complexity in supramolecular polymerization has prompted the finding of novel monomer designs able to stabilize kinetically trapped species and generate supramolecular polymorphs. In the present work, the exploitation of the Z/E (geometrical) isomerism of squaramide (SQ) units to produce various self-assembled isoforms and complex supramolecular polymerization pathways in methylcyclohexane/CHCl3 mixtures is reported for the first time. This is achieved by using a new bissquaramidic macrocycle (MSq) that self-assembles into two markedly different thermodynamic aggregates, AggA (discrete cyclic structures) and AggB (fibrillar structures), depending on the solven…

Supramolecular chemistry02 engineering and technology010402 general chemistry01 natural sciencesPolymerizationBiomaterialschemistry.chemical_compoundIsomerismSpectroscopy Fourier Transform InfraredGeneral Materials ScienceConformational isomerismchemistry.chemical_classificationQuinineHydrogen bondSquaramideHydrogen BondingGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesSupramolecular polymersCrystallographyMonomerPolymerizationchemistryMethylcyclohexane0210 nano-technologyBiotechnologySmall
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A Stereochemically Driven Supramolecular Polymerisation

2018

Anthracyclines self-assemble in water into dimers. In the presence of sufficiently high salt (NaCl) concentrations, solutions of the antibiotic doxorubicin, but not those of the closely related molecules daunomycin and epirubicin, turn into gels barely compatible with the presence of small oligomers. The use of spectroscopic, scattering, imaging and computational techniques, allowed light to be shed on the self-assembly process that triggered doxorubicin gelification. A complex picture emerged, with doxorubicin molecules assembled into long, highly chiral, supramolecular aggregates made of hundreds of units, showing redshifted fluorescence spectra, very short fluorescence lifetimes and smal…

Supramolecular chemistry02 engineering and technology010402 general chemistryPhotochemistrydoxorubicin01 natural sciencesCatalysisTurn (biochemistry)chemistry.chemical_compoundMolecular dynamicsanthracyclines; doxorubicin; fluorescence; circular dichroism; SAXS; molecular dynamicsMoleculeanthracyclinesScatteringOrganic ChemistrySAXSGeneral Chemistry021001 nanoscience & nanotechnologyFluorescencemolecular dynamicscircular dichroism0104 chemical sciencesMonomerchemistryPolymerizationfluorescence0210 nano-technologyChemistry - A European Journal
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Synthesis, UV/vis, FT-IR and Mössbauer spectroscopic characterization and molecular structure of the Bis[4-(2-aminoethyl)morpholine](tetrakis(4-metox…

2016

International audience; The synthesis, the UV-visible, FT-IR and Mossbauer spectroscopy and the crystal structure characterizations of the bis[4-(2-Aminoethyl)morpholine]tetrakis(4-metoxyphenyl)porphy-rinato)iron(II) complex are described. The title compound crystallizes in the triclinic, space group P-1, with a = 11.1253(4) angstrom, b = 11.2379(4) angstrom, c = 11.5488(4) angstrom, alpha = 72.304(2)degrees, beta = 86.002(2)degrees gamma = 72.066(2)degrees, V = 1308.28(8) angstrom(3), Z = 1. The Mossbauer data are consistent with an iron(II) low-spin (S = 0) porphyin species. The spin-state is confirmed by the value of the average equatorial iron-nitrogen pyrrole distance (Fe-Np = 1.988(2)…

Supramolecular chemistry02 engineering and technologyCrystal structureTriclinic crystal system010402 general chemistryspin01 natural sciencesUV-visible[ CHIM ] Chemical SciencesAnalytical ChemistryInorganic ChemistryMossbauerchemistry.chemical_compoundMorpholineMössbauer spectroscopy[CHIM]Chemical SciencesSpectroscopyPyrroleHydrogen bondOrganic Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesX-ray diffractionCrystallographychemistryIron porphyrin complexX-ray crystallography0210 nano-technologycrystal-structures
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Carbohydrate-supramolecular gels : adsorbents for chromium(VI) removal from wastewater.

2019

Abstract Hypothesis To overcome the contamination of water by heavy metals the adsorption of the pollutant on gel phases is an attractive solution since gels are inexpensive, potentially highly efficient and form a distinct phase while allowing diffusion of the contaminated water throughout the material. This work tests the chromium(VI) adsorbent capacity of new supramolecular gels for Chromium(VI) removal from wastewater. Experiments First hydrophobic imidazolium salts of carbohydrate anions were synthesised as new gelators. Subsequently, they were dissolved in a solvent by heating and, after cooling overnight, to give the formation of supramolecular gels. The properties of the resulting g…

Supramolecular chemistryInfrared spectroscopychemistry.chemical_element02 engineering and technologychemisorption010402 general chemistry01 natural sciencesBiomaterialsChromiumchemistry.chemical_compoundColloid and Surface ChemistryAdsorptionThermal stabilityHexavalent chromiumhexavalent chromiumChemistrySettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolventcarbohydrate gelatorwastewater treatmentChemical engineeringreduction of toxic metalSelf-healing hydrogelsSupramolecular gel0210 nano-technologyenvironmental remediation
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