Search results for "ACETYLENE"

showing 10 items of 143 documents

On-surface synthesis on a bulk insulator surface

2018

On-surface synthesis has rapidly emerged as a most promising approach to prepare functional molecular structures directly on a support surface. Compared to solution synthesis, performing chemical reactions on a surface offers several exciting new options: due to the absence of a solvent, reactions can be envisioned that are otherwise not feasible due to the insolubility of the reaction product. Perhaps even more important, the confinement to a two-dimensional surface might enable reaction pathways that are not accessible otherwise. Consequently, on-surface synthesis has attracted great attention in the last decade, with an impressive number of classical reactions transferred to a surface as…

Materials scienceInsulator (electricity)02 engineering and technology010402 general chemistryF160 Organic Chemistry53001 natural sciencesChemical reactionUllmann reactionMetalchemistry.chemical_compoundGeneral Materials ScienceF200 Materials ScienceDiacetylene021001 nanoscience & nanotechnologyCondensed Matter PhysicsCycloaddition0104 chemical sciencesPolymerizationchemistryChemical physicsvisual_artvisual_art.visual_art_mediumF343 Computational PhysicsF320 Chemical PhysicsSupport surface0210 nano-technologyJournal of Physics: Condensed Matter
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Rapid one-pot propargylamine synthesis by plasmon mediated catalysis with gold nanoparticles on ZnO under ambient conditions

2013

Surface plasmon excitation of gold nanoparticles on ZnO in the presence of an aldehyde, an amine and phenylacetylene led to rapid and selective formation of propargylamines with good yields (50-95%) at room temperature. Plasmon mediated catalysis is the best available route for this ternary coupling.

Materials scienceMetal Nanoparticles010402 general chemistryPhotochemistry01 natural sciencesAldehydeCatalysisCatalysischemistry.chemical_compoundMaterials ChemistrySurface plasmon excitationAminesPlasmonchemistry.chemical_classificationAldehydesPropylamines010405 organic chemistryTemperatureMetals and AlloysGeneral Chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPargylinechemistryPhenylacetyleneColloidal goldAlkynesCeramics and CompositesAmine gas treatingGoldZinc OxideTernary operationChemical Communications
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Surface characterization of functional poly(diacetylene) and poly(butadiene) mono- and multilayers

1982

The surface properties of Langmuir-Blodgett mono- and multilayers of a variety of amphiphilic poly(diacetylene)s and poly(butadiene)s were investigated by contact angle, streaming potentialζ, ellipsometry, and X-ray photoelectron spectroscopic (XPS) measurements. Captive air and octane angles varied between approximately 60° and 105° for hydrophobicx-layers and 31° to 46° for hydrophilic surfaces depending on the particular head group, whereas advancing angles determined via the vertical plate method are considerably higher. Negative streaming potentials were obtained for all surfaces. Positively charged monolayers yielded less negativeζ- potential values (−28 mV) than negatively charged (−…

Materials sciencePolymers and PlasticsDiacetyleneAnalytical chemistryStreaming currentContact anglechemistry.chemical_compoundColloid and Surface ChemistryX-ray photoelectron spectroscopyPolymerizationchemistryEllipsometryMonolayerMaterials ChemistryPhysical and Theoretical ChemistryOctaneColloid and Polymer Science
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Spin Crossover Metal-Organic Frameworks with Inserted Photoactive Guests: On the Quest to Control the Spin State by Photoisomerization

2021

International audience; Three Hofmann-like metal-organic frameworks {Fe(bpac)[Pt(CN)4]}•G (bpac=1,2-bis(4-pyridyl)acetylene) were synthesized with photoisomerizable guest molecules (G = trans-azobenzene, trans-stilbene or cis-stilbene) and were characterized by elemental analysis, thermogravimetry and powder X-ray diffraction. The insertion of guest molecules and their conformation were inferred from Raman and FTIR spectra and from single-crystal X-ray diffraction and confronted with computational simulation. The magnetic and photomagnetic behaviors of the framework are significantly altered by the different guest molecules and different conformations. On the other hand, photoisomerization …

Materials scienceSpin statesPhotoisomerization02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesInorganic ChemistryThermogravimetryCrystallographychemistry.chemical_compoundsymbols.namesakeAcetylenechemistrySpin crossoversymbols[CHIM.CRIS]Chemical Sciences/CristallographyMoleculeMetal-organic framework[CHIM.COOR]Chemical Sciences/Coordination chemistry0210 nano-technologyRaman spectroscopy
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Diacetylene Linked Anthracene Oligomers Synthesized by One-Shot Homocoupling of Trimethylsilyl on Cu(111)

2018

On-surface chemical reaction has become a very powerful technique to conjugate small precursor molecules and several reactions have been proposed with the aim to fabricate functional nanostructures on surfaces. Here we present an unforeseen adsorption mode of 9,10-bis-((trimethylsilyl)ethynyl)anthracene on a Cu(111)surface and the resulting one-shot desilylative homocoupling of of the adsorbate by annealing at 400 K. With a combination of high-resolution atomic force microscopy and density functional theory calculations, we found that the triple bonds and silicon atoms of the monomer chemically interact with the copper surface. After the oligomerization, we discovered that the anthracene un…

Materials scienceTrimethylsilylta221General Physics and Astronomy02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesChemical reactionchemistry.chemical_compoundAdsorptionMoleculeGeneral Materials Scienceon-surface chemical reactionAnthraceneatomic force microscopyDiacetyleneanthraceneGlaser couplingGeneral Engineeringtrimethylsilyl021001 nanoscience & nanotechnologyTriple bond0104 chemical sciencesMonomerchemistry0210 nano-technologyACS Nano
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The extraction of negative carbon ions from a volume cusp ion source

2017

Acetylene and carbon dioxide gases are used in a filament-powered volume-cusp ion source to produce negative carbon ions for the purpose of carbon implantation for gettering applications. The beam was extracted to an energy of 25 keV and the composition was analyzed with a spectrometer system consisting of a 90° dipole magnet and a pair of slits. It is found that acetylene produces mostly C−2 ions (up to 92 µA), while carbon dioxide produces mostly O− with only trace amounts of C−. Maximum C−2 current was achieved with 400 W of arc power and, the beam current and composition were found to be highly dependent on the pressure in the source. The beam properties as a function of source settings…

Materials scienceta114SpectrometerionithiiliAnalytical chemistrychemistry.chemical_elementPlasmaplasmatekniikkaIon sourceIonsymbols.namesakechemistry.chemical_compoundcarbon ionsion sourcesvolume cusp ion sourceAcetylenechemistryPhysics::Plasma PhysicssymbolsLangmuir probeCarbonBeam (structure)
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A New Heterogeneous Catalyst Obtained via Supramolecular Decoration of Graphene with a Pd2+ Azamacrocyclic Complex

2019

A new G-(H2L)-Pd heterogeneous catalyst has been prepared via a self-assembly process consisting in the spontaneous adsorption, in water at room temperature, of a macrocyclic H2L ligand on graphene (G) (G + H2L = G-(H2L)), followed by decoration of the macrocycle with Pd2+ ions (G-(H2L) + Pd2+ = G-(H2L)-Pd) under the same mild conditions. This supramolecular approach is a sustainable (green) procedure that preserves the special characteristics of graphene and furnishes an efficient catalyst for the Cu-free Sonogashira cross coupling reaction between iodobenzene and phenylacetylene. Indeed, G-(H2L)-Pd shows an excellent conversion (90%) of reactants into diphenylacetylene under mild conditio…

Models MolecularChemical PhenomenaIodobenzeneMolecular ConformationPharmaceutical ScienceSonogashira couplingLigands010402 general chemistryHeterogeneous catalysiscross coupling01 natural sciencesArticleCoupling reactionAnalytical Chemistrylaw.inventionCatalysislcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryCoordination ComplexeslawDrug DiscoveryPolymer chemistryPhysical and Theoretical ChemistryDiphenylacetyleneMolecular Structurecatalysis010405 organic chemistryGrapheneSpectrum AnalysisOrganic ChemistrySonogashirapalladium catalystHydrogen-Ion Concentrationsupramolecular interactions0104 chemical sciencesSolutionsazamacrocycleschemistryPhenylacetyleneChemistry (miscellaneous)surface adsorptionMolecular MedicineGraphitecatalysis palladium catalyst; Sonogashira graphenePalladiumMolecules
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Aminobisphenolate supported tungsten disulphido and dithiolene complexes

2015

Dioxotungsten(vi) complexes with tetradentate amino bisphenolates were converted into the corresponding Cs-symmetric amino bisphenolate disulphido complexes by a reaction with either Lawesson's reagent or P2S5. Further reaction with diethyl acetylenedicarboxylate leads to the formation of diamagnetic tungsten(iv) dithiolene compounds. The syntheses, crystal structures, spectroscopic and electrochemical characterization of such disulphido and dithiolene complexes are presented.

Models MolecularInorganic chemistryMolecular Conformationchemistry.chemical_elementOxidestungsten disulphidoCrystal structureSulfidesTungstenElectrochemistryTungstenInorganic ChemistryDiethyl acetylenedicarboxylatechemistryReagentPolymer chemistryElectrochemistryHydroxybenzoatesOrganometallic Compoundsdithiolene complexesta116Dalton Transactions
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Organometallic Oligomers Based on Bis(arylacetylide)bis(P-chirogenic phosphine)platinum(II) Complexes: Synthesis and Photonic Properties

2013

A series of P-chirogenic oligomers of the type (-C≡C-aryl-C≡C-PtL2-)n [L = (R)- and (S)-P(Ph)(iPr)(C17H35); aryl = 1,4-benzene, 2,1,3-benzothiadiazole] along the corresponding achiral analogues (L = PBu3) and model complexes PhC≡CPtL2C≡CPh were prepared from the ephedrine strategy and were fully characterized [(1)H, (31)P NMR; IR; small-angle X-ray scattering (SAXS); gel permeation chromatography (GPC); thermal gravimetric analysis (TGA); circular dichroism, UV-vis, and luminescence spectroscopy; photophysics, and degree of anisotropy measurements]. From the CD measurements, the chiral environment of the phosphine ligands is modestly felt by the aryl moieties. Concurrently, the TGA shows th…

Models MolecularPhotonsCircular dichroismThermogravimetric analysisMolecular StructureOrganoplatinum CompoundsAcetylenePhosphinesSmall-angle X-ray scatteringChemistryLigandArylMolecular Dynamics SimulationPhotochemistryInorganic ChemistryGel permeation chromatographychemistry.chemical_compoundPolymer chemistryPhysical and Theoretical ChemistryLuminescencePhosphineInorganic Chemistry
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A DFT study of the ionic [2+2] cycloaddition reactions of keteniminium cations with terminal acetylenes

2015

Abstract The molecular mechanism of the ionic [2+2] cycloaddition (I-22CA) reactions of a keteniminium cation (KC) with acetylene and propyne has been investigated using DFT methods at the MPWB1K/6-311G(d,p) level. These I-22CA reactions take place via a two-step mechanism. The first step is the nucleophilic attack of these alkynes on the central carbon of KC, yielding cyclopropene intermediates, while the second step corresponds to the conversion of these intermediates into more stable cyclobuteniminium cations (CCs). The first step is the rate-determining step, while the second step is responsible for the formation of the two regioisomeric CCs experimentally observed in the reaction with …

Organic ChemistryIonic bondingCyclopropenePropynePhotochemistryBiochemistryCycloadditionchemistry.chemical_compoundNucleophilechemistryAcetyleneComputational chemistryDrug DiscoveryElectrophileReactivity (chemistry)Tetrahedron
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