Search results for "Silane"

showing 10 items of 173 documents

Bridging vs. Chelating Coordination Modes of Vinylsilanes in CuIπ-Complexes: Structure and Stability

2013

Two new copper(I) olefin complexes, [Cu6Cl6(MTrVS)2] (1) and [Cu2Cl2(DMVSP)2] (2), of tridentate bridging methyltrivinylsilane (MTrVS) and bidentate chelating 2-[dimethyl(vinyl)silyl]pyridine (DMVSP) have been synthesized and characterized by single-crystal X-ray structure analysis, IR and 1H NMR spectroscopy. It has been shown that using the alkenylsilanes with required electronic properties, molecular symmetry and conformational flexibility, it is possible to control the formation of optimal copper(I) halide oligomers. The obtained results, together with relevant literature data, also illustrate how the coordination mode of vinylsilanes is related to Cu–(C=C) bond strengthening and, conse…

Olefin fiberSilanesDenticityChemistryStereochemistrychemistry.chemical_elementCrystal structureCopperInorganic Chemistrychemistry.chemical_compoundCrystallographyPyridineThermal stabilityGroup 2 organometallic chemistryZeitschrift für anorganische und allgemeine Chemie
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Theoretical study of the effect of substituent and backbone conformation on the electronic properties of symmetrically substituted poly(di‐n‐alkylsil…

1994

We present the results of ab initio 3‐21G∗ geometry optimizations and valence effective Hamiltonian (VEH) band structure calculations aimed at determining the evolution of the geometric and electronic (ionization potential, electron affinities, and band gaps) properties of all‐trans poly(dimethylsilane), poly(diethylsilane), poly(di‐n‐propylsilane), and poly(di‐n‐butylsilane) when increasing the size of the alkyl group. In the latter polymer, we have also studied the 7/3 conformation, in order to analyze the effect of the backbone conformation on the geometric and electronic structure. The VEH ionization potentials of all‐trans poly(di‐n‐alkylsilanes) are almost equal, and as experimental p…

OptimizationEnergy GapPropyl CompoundsBand gapAb initioSubstituentGeometryGeneral Physics and AstronomyElectronic structurechemistry.chemical_compoundAb initio quantum chemistry methodsComputational chemistryMethyl CompoundsConformational ChangesPhysical and Theoretical ChemistryBand Structure:FÍSICA::Química física [UNESCO]Electronic band structureAlkyl Compounds ; Silanes ; Organic Polymers ; Conformational Changes ; Ab Initio Calculations ; Geometry ; Optimization ; Band Structure ; Affinity ; Ionization Potential ; Energy Gap ; Methyl Compounds ; Ethyl Compounds ; Propyl CompoundsDimethylsilaneOrganic PolymersSilanesUNESCO::FÍSICA::Química físicaCrystallographyAlkyl CompoundsIonization PotentialAffinitychemistryEthyl CompoundsIonization energyAb Initio Calculations
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Synthesis of silacyclopent-2-en-4-ols via intramolecular [2 + 2] photocycloaddition of benzoyl(allyl)silanes

2019

Organosilicon compounds are versatile units with a wide range of uses from medicinal chemistry to the field of organic electronics. An unprecedented method for the synthesis of novel diaryl-substituted silacyclopentenols via blue-light promoted intramolecular [2 + 2] photocycloaddition of acyl silanes is herein disclosed. Additionally, the present findings demonstrate the influence of the olefin substituents in controlling the regioselectivity of the intramolecular Paterno–Buchi reaction, providing silacycles different from previously reported ones. The high degree of functionalization of these compounds makes them attractive precursors to other synthetically challenging silacyclopentanes.

Organic electronicsOlefin fiberSilanes010405 organic chemistryOrganic Chemistry116 Chemical sciencesRegioselectivity010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical scienceschemistry.chemical_compoundchemistryIntramolecular forceSurface modificationOrganosilicon
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Connecting Curable Siloxanes to Luminescent Organic Semiconductors - Monomers for Functional Hybrid Materials

2006

ABSTRACTLuminescent stilbenoid chromophores with two alkoxysilane end groups are prepared via hydrosilylation or condensation / reduction of substituted 5-ring OPVs with hydro- and aminopropylsilanes. Chromophore and curable units are connected via flexible spacers. To obtain compounds with a rigid connection between silane and π-system, iodo- or bromo-OPVs were coupled to alkoxysilanes carrying vinyl- or p-vinylphenyl moieties under Heck conditions. This approach allowed a combined connection of the chromophore to the silane moiety with an extension of the π-system. Hydrolysis of the alkoxysilanes yields silanols condensing to curable three-dimensional networks, thus allowing the transform…

Organic semiconductorchemistry.chemical_compoundMonomerMaterials sciencechemistryPolymerizationHydrosilylationPolymer chemistryMoietyChromophoreHybrid materialSilaneMRS Proceedings
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Performance of porous silica layers in open-tubular columns for liquid chromatography

1989

Abstract Progress has been made in the preparation of porous silica layers in fused-silica capillaries for open-tubular liquid chromatography. The porous silica layer is prepared by (i) static coating of the silica precursor, polyethoxysiloxane (PES), followed by (ii) converting the PES film into a porous silica layer with ammonia solution. The porous silica layer can be easily modified by silane reagents commonly used in packed column high-performance liquid chromatography. The performance of the silica layer with the different phase systems was tested with polyaromatic hydrocarbons and derivatized amino acids as samples.

Packed bedChromatographyOrganic Chemistrytechnology industry and agricultureGeneral Medicinerespiratory systemPorous glassBiochemistrySilaneAnalytical Chemistrychemistry.chemical_compoundchemistryReagentPorosityLayer (electronics)Fumed silicaHydrophobic silicaJournal of Chromatography A
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The hot bands of silane between 2120 and 2270cm−1

2005

Abstract The infrared spectrum of the SiH 4 molecule has been recorded between 2040 and 2320 cm −1 using the high-resolution Fourier interferometer of the Laboratoire de Photophysique Moleculaire ( Orsay , France ). The resolution was 5.4 × 10 −3  cm −1 . In this region, many lines were previously analyzed and assigned to the ν 1 / ν 3 stretching dyad of 28 SiH 4 , 29 SiH 4 , and 30 SiH 4 molecules [J. Mol. Spectrosc. 143 (1990) 35]. However, several lines in the spectrum were not assigned. The results obtained in our previous study [J. Mol. Spectrosc. 197 (1999) 307] of the infrared spectrum of 28 SiH 4 , in the bending-stretching tetrad region at 3100 cm −1 , enabled us to assign 204 of t…

PhysicsInfraredAnalytical chemistryTetrahedral molecular geometrySilaneAtomic and Molecular Physics and Opticschemistry.chemical_compoundsymbols.namesakeFormalism (philosophy of mathematics)Fourier transformchemistrysymbolsMoleculePhysical and Theoretical ChemistryHamiltonian (quantum mechanics)TetradSpectroscopyJournal of Molecular Spectroscopy
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Double modulation sideband spectroscopy: μ0, μ24, and μ44 of 28SiH4

1992

Abstract The linear Stark effect within the ν 2 ν 4 dyad of the main isotopomer of silane, 28 SiH 4 , has been investigated by applying the saturation technique as well as IR-IR double resonance. From 35 transitions, two vibration-induced dipole moment parameters and the centrifugal distortion moment have been determined as μ 0 = 1.357(12) × 10 −5 D, μ 24 = 2.391(31) × 10 −2 D, and μ 44 = −1.261(17) × 10 −2 D employing the Stark coefficients calculated by the procedure of Loete.

PhysicsSidebandSilaneAtomic and Molecular Physics and OpticsIsotopomerssymbols.namesakeDipolechemistry.chemical_compoundNuclear magnetic resonanceStark effectchemistrysymbolsPhysical and Theoretical ChemistryAtomic physicsSaturation (chemistry)SpectroscopySpectroscopyJournal of Molecular Spectroscopy
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Highly selective and sensitive chromo-fluorogenic detection of the Tetryl explosive using functional silica nanoparticles

2011

Silica nanoparticles containing polyamines and thiol groups have been used as probes for the selective detection of Tetryl. © 2011 The Royal Society of Chemistry.

PolyamineINGENIERIA DE LA CONSTRUCCIONUnclassified drugNanoparticlePhotochemistryColorimetry (chemical method)Nitrobenzenechemistry.chemical_compoundNanoparticleQUIMICA ORGANICAChemical structureSilicon dioxidePolyaminesMaterials ChemistryChemical analysischemistry.chemical_classificationAniline CompoundsChemistryMetals and Alloysrespiratory systemTetrylSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsThiolColorimetryDyeExplosive materialSilicon dioxideChemical structureArticleCatalysisThiol groupBinding site246 trinitrophenylmethylnitramineExplosive AgentsExplosiveReaction analysisQUIMICA ANALITICASulfhydryl CompoundsNitrobenzenesSensorFluorescent DyesFluorescent dyeQUIMICA INORGANICAGeneral ChemistrySilane derivativeCombinatorial chemistryChromogenic substrateCeramics and CompositesNanoparticlesChemical Communications
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Characterization of Polyorganosiloxane Nanoparticles in Aqueous Dispersion by Asymmetrical Flow Field-Flow Fractionation

2001

The advantages of asymmetrical flow field-flow fractionation (AF-FFF) for the characterization of aqueous dispersions of spherical polyorganosiloxane nanoparticles are discussed. With AF-FFF it was possible to obtain information about the synthesis, which is based on the hydrolysis and condensation of alkylalkoxysilanes in aqueous dispersion, and the average size of the spherical nanoparticles in the complex mixture in the presence of excess surfactant. The results are compared to measurements performed with dynamic light scattering (DLS). The size of the nanoparticles increases as a function of the amount of added monomer. Particles with radii between 2 and 50 nm are observed. If only the …

Polymers and PlasticsMethyltrimethoxysilaneOrganic ChemistryCondensationNanoparticleRadiusFractionationInorganic Chemistrychemistry.chemical_compoundMonomerchemistryDynamic light scatteringPulmonary surfactantChemical engineeringPolymer chemistryMaterials ChemistryMacromolecules
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Elastomeric Organosilicon Micronetworks

1997

Trifunctional methyltrimethoxysilane and bifunctional dimethyldimethoxysilane monomers were cocondensed in water in the presence of surfactant. Strictly spherical micronetworks of narrow size distribution were obtained for particle sizes 10 nm < R < 30 nm. By special “endcapping” reactions all reactive SiOH groups were removed quantitatively, and the resulting micronetworks become soluble in common organic solvents like toluene, THF, or chloroform. For contents of trifunctional monomer larger than 50 mol % the particles do not swell irrespective of the choice of the solvent, whereas for lower mole fractions of trimethoxysilane an increasing swelling ratio is observed. Below 2.5 mol % trifun…

Polymers and PlasticsMethyltrimethoxysilaneOrganic ChemistryMole fractionTolueneInorganic ChemistrySolventchemistry.chemical_compoundMonomerchemistryEndcappingPolymer chemistryMaterials ChemistryBifunctionalOrganosiliconMacromolecules
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