Search results for "Silane"

showing 10 items of 173 documents

CCDC 686635: Experimental Crystal Structure Determination

2009

Related Article: S.-O.Hauber, M.Niemeyer|2008|Z.Anorg.Allg.Chem.|634|2594|doi:10.1002/zaac.200800291

((Biphenyl-2-yl)dimethylsilyl)-tris(trimethylsilyl)silaneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

CCDC 105692: Experimental Crystal Structure Determination

1999

Related Article: K.Hensen, T.Stumpf, M.Bolte, C.Nather, H.Fleischer|1998|J.Am.Chem.Soc.|120|10402|doi:10.1021/ja981016g

(Dihydro-tetrapyridyl)silane dichloride chloroform solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct

Gas-Phase Synthesis of the Elusive Trisilicontetrahydride Species (Si3H4)

2016

The bimolecular gas-phase reaction of ground-state atomic silicon (Si; 3P) with disilane (Si2H6; 1A1g) was explored under single-collision conditions in a crossed molecular beam machine at a collision energy of 21 kJ mol–1. Combined with electronic structure calculations, the results suggest the formation of Si3H4 isomer(s) along with molecular hydrogen via indirect scattering dynamics through Si3H6 collision complex(es) and intersystem crossing from the triplet to the singlet surface. The nonadiabatic reaction dynamics can synthesize the energetically accessible singlet Si3H4 isomers in overall exoergic reaction(s) (−93 ± 21 kJ mol–1). All reasonable reaction products are either cyclic or …

010304 chemical physicsElectronic structure010402 general chemistryPhotochemistry01 natural sciences0104 chemical sciencesChemical DynamicsCrossed molecular beamchemistry.chemical_compoundIntersystem crossingchemistryReaction dynamics0103 physical sciencesGeneral Materials ScienceSinglet stateDisilanePhysical and Theoretical ChemistryIsomerizationThe Journal of Physical Chemistry Letters
researchProduct

Performance of different C18 columns in reversed-phase liquid chromatography with hydro-organic and micellar-organic mobile phases

2014

Column selection in reversed-phase liquid chromatography (RPLC) can become a challenge if the target compounds interact with the silica-based packing. One of such interactions is the attraction of cationic solutes to the free silanols in silica-based columns, which is a slow sorption-desorption interaction process that gives rise to tailed and broad peaks. The effect of silanols is minimised by the addition of a competing agent in the mobile phase, such as the anionic surfactant sodium dodecyl sulphate (SDS). In micellar-organic RPLC, the adsorption of an approximately fixed amount of SDS monomers gives rise to a stable modified stationary phase, with properties remarkably different from th…

AcetonitrilesAdrenergic beta-AntagonistsBiochemistryAnalytical ChemistrySurface-Active AgentsAdsorptionPulmonary surfactantPhenolsPhase (matter)Sodium dodecyl sulphateAcetonitrileMicellesChromatography Reverse-PhaseChromatographyElutionChemistryOrganic ChemistryCationic polymerizationC18 columnsSodium Dodecyl SulfateWaterGeneral MedicineReversed-phase chromatographySilanesMicellar liquid chromatographyβ-BlockersAdsorptionSelectivityMicellar liquid chromatography
researchProduct

Performance of amines as silanol suppressors in reversed-phase liquid chromatography

2016

In reversed-phase liquid chromatography, cationic basic compounds yield broad and asymmetrical peaks, as a result of their ionic interaction with the anionic free silanol groups present in the silica-based stationary phases (commonly derivatised with C18 groups). A simple way to improve the peak shape is the addition to the hydro-organic mobile phase of a reagent (usually called additive) with cationic character. This associates with the stationary phase to prevent the access of analytes to the free silanol groups. Cationic additives may interact electrostatically with the anionic silanols. The hydrophobic region of the additive may also associate with the alkyl chains bound to the stationa…

Adrenergic beta-AntagonistsIonic Liquids010402 general chemistry01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundHexylamineEndcappingPhase (matter)BoratesAminesChromatography Reverse-PhaseChromatography010401 analytical chemistryOrganic ChemistryImidazolesCationic polymerizationGeneral MedicineReversed-phase chromatographySilanes0104 chemical sciencesSilanolchemistryIonic liquidPentylamineHydrophobic and Hydrophilic InteractionsJournal of Chromatography A
researchProduct

3D-printing-assisted fabrication of chitosan scaffolds from different sources and cross-linkers for dental tissue engineering

2021

The aim of the present study was to fabricate and characterise chitosan scaffolds from animal and fungal sources, with or without gelatine as a co-polymer, and cross-linked to 3-glycidyloxyproply trimethoxysilane (GPTMS) or genipin for application in dental root tissue engineering. Chitosan-based scaffolds were prepared by the emulsion freeze-drying technique. Scanning electron microscopy (SEM) and nano-focus computed tomography (nano-CT) were used to characterise scaffold microstructure. Chemical composition and cross-linking were evaluated by Fourier transform infrared-attenuated total reflectance spectroscopy. Compression tests were performed to evaluate scaffold mechanical properties. S…

AdultMaleScaffoldMaterials scienceRD1-811AdolescentCompressive StrengthScanning electron microscopeSimulated body fluid0206 medical engineeringBiocompatible MaterialsDiseases of the musculoskeletal system02 engineering and technologyApatiteChitosanYoung Adultchemistry.chemical_compoundTissue engineeringfungal chitosanDental pulp stem cellsMaterials TestingHumansIridoidsCells CulturedDental PulpChitosanTissue EngineeringTissue ScaffoldsStem Cellstechnology industry and agricultureSilanes020601 biomedical engineeringdental pulp stem cellsRC925-935chemistryvisual_artPrinting Three-Dimensionalvisual_art.visual_art_mediumGenipinSurgeryFemalePorosityBiomedical engineeringEuropean Cells and Materials
researchProduct

Electronic excitations of 1,4-disilyl-substituted 1,4-disilabicycloalkanes: a MS-CASPT2 study of the influence of cage size.

2007

We present a multistate complete active space second-order perturbation theory computational study aimed to predict the low-lying electronic excitations of four compounds that can be viewed as two disilane units connected through alkane bridges in a bicyclic cage. The analysis has focused on 1,4-disilyl-1,4-disilabicyclo[2.2.1]heptane (1a), 1,4-bis(trimethylsilyl)-1,4-disilabicyclo[2.2.1]heptane (1b), 1,4-disilyl-1,4-disilabicyclo[2.1.1]hexane (2a), and 1,4-bis(trimethylsilyl)-1,4-disilabicyclo[2.1.1]hexane (2b). The aim has been to find out the nature of the lowest excitations with significant oscillator strengths and to investigate how the cage size affects the excitation energies and the…

Alkanechemistry.chemical_classificationHeptaneBicyclic moleculeTrimethylsilylMolecular StructureElectronsHexanechemistry.chemical_compoundchemistryModels ChemicalComputational chemistryPhysical chemistryQuantum TheoryOrganosilicon CompoundsComplete active spaceDisilanePhysical and Theoretical ChemistryExcitationThe journal of physical chemistry. A
researchProduct

New insights in the formation of silanol defects in silicalite-1 by water intrusion under high pressure.

2010

International audience; The "water-silicalite-1" system is known to act as a molecular spring. The successive intrusion-extrusion cycles of liquid water in small crystallites (6 × 3 × 0.5 μm(3)) of hydrophobic silicalite-1 were studied by volumetric and calorimetric techniques. The experiments displayed a decrease of the intrusion pressure between the first intrusion-extrusion cycle and the consecutive ones, whereas the extrusion pressures remained unchanged. However, neither XRD studies nor SEM observations revealed any structural and morphological modifications of silicalite-1 at the long-range order. Such a shift in the value of the intrusion pressure after the first water intrusion-extr…

Analytical chemistryGeneral Physics and AstronomyInfrared spectroscopy02 engineering and technologyCalorimetry010402 general chemistryMolecular sieve01 natural scienceschemistry.chemical_compoundX-Ray DiffractionSpectroscopy Fourier Transform InfraredPressure[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyPhysical and Theoretical ChemistryFourier transform infrared spectroscopyZeoliteSilicatesWaterSilanes021001 nanoscience & nanotechnology0104 chemical sciencesSilanolchemistryChemical engineeringSiloxaneX-ray crystallographyZeolitesCrystallite0210 nano-technologyCrystallizationPhysical chemistry chemical physics : PCCP
researchProduct

A solid device based on doped hybrid composites for controlling the dosage of the biocide N-(3-aminopropyl)-N-dodecyl-1,3-propanediamine in industria…

2015

A colorimetric composite device is proposed to determine the widely used biocide N-(3-aminopropyl)-N-dodecyl-1,3-propanediamine (ADP).This sensing device is based on a film of 1,2-Naphthoquinone-4-sulfonate (NQS) embedded into polydimethylsiloxane-tetraethylortosilicate-SiO2 nanoparticles composite (PDMS-TEOS-SiO2NPs). Semiquantitative analysis can be performed by visual inspection. Digitalized image or diffuse reflectance (DR) measurements can be carried out for quantitative analysis. Satisfactory detection limit (0.018%, w/v) and relative standard deviations <12% were achieved. The proposed device has been applied for the determination of ADP in detergent industrial formulations with reco…

BiocideChemistry PharmaceuticalDetergentsComposite numberAnalytical chemistryNQSNanoparticle02 engineering and technology01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundDimethylpolysiloxanesDetection limitPropylaminesPolydimethylsiloxaneChemistry010401 analytical chemistrySilanesSilicon Dioxide021001 nanoscience & nanotechnology0104 chemical sciencesKineticsColorimetryDiffuse reflection0210 nano-technologyQuantitative analysis (chemistry)DisinfectantsNaphthoquinonesTalanta
researchProduct

Palladium-catalyzed formation and reactions of iodo- and bromosiloxane intermediates

2012

Polysiloxanes are useful materials because of their functionality, such as high thermal stability, electrical resistance, and hydrophobicity. In this regard, we studied palladium-catalyzed formation of iodo-and bromopolysiloxanes from two types of hydrosiloxanes, alpha,omega-dihydropoly(dimethylsiloxane) (1) and cyclotetra(hydromethylsiloxane) (2), and their reactions. Treatment of 1 with mixtures of cyclic ethers or lactones and MeI or allylBr in the presence of a catalytic amount of PdCl2 gave the corresponding alpha,omega-bis(haloalkoxy and haloalkanoyloxy) poly(dimethylsiloxane)s in good yields, via iodo-and bromopoly(dimethylsiloxane) intermediates. Transformation of the iodobutoxy-ter…

BoromosilaneIodosilanechemistry.chemical_element430BiochemistryCatalysisInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryThermal stabilityPhysical and Theoretical Chemistrychemistry.chemical_classification430Quenching (fluorescence)EthanolOrganic ChemistryPolysiloxanePolymerLactonechemistryCyclic etherPalladium catalystCyclic etherLactonePalladiumJournal of Organometallic Chemistry
researchProduct