Search results for "Silylation"

showing 10 items of 97 documents

Three 2,5-dialkoxy-1,4-diethynylbenzene derivatives

2008

2,5-Dieth­oxy-1,4-bis­[(trimethyl­silyl)ethyn­yl]benzene, C20H30O2Si2, (I), constitutes one of the first structurally characterized examples of a family of compounds, viz. the 2,5-dialk­oxy-1,4-bis­[(trimethyl­silyl)ethyn­yl]benzene derivatives, used in the preparation of oligo(phenyl­ene­ethynylene)s via Pd/Cu-catalysed cross-coupling. 2,5-Dieth­oxy-1,4-diethynylbenzene, C14H14O2, (II), results from protodesilylation of (I). 1,4-Diethynyl-2,5-bis­(hept­yloxy)benzene, C24H34O2, (III), is a long alk­yloxy chain analogue of (II). The molecules of compounds (I)–(III) are located on sites with crystallographic inversion symmetry. The large substituents either in the alkynyl group or in the benz…

SilylationStereochemistryThree 25-dialkoxy-14-diethynylbenzene derivativesEtherGeneral MedicineCrystal structure.Ring (chemistry)Medicinal chemistryGeneral Biochemistry Genetics and Molecular BiologyFaculdade de Ciências Exatas e da Engenhariachemistry.chemical_compoundsymbols.namesakechemistryAtomsymbolsMoleculeVan der Waals radiusBenzeneActa Crystallographica Section C Crystal Structure Communications
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1,8-Bis[3-(triethoxysilyl)propyl]-1,8-diazoniatricyclo[9.3.1.14,8]hexadecane diiodide

2009

The organic molecule of title compound, C30H66N4O6Si22+·2I−, is located around a centre of symmetry. The structure exhibits disorder of the triethoxy groups with the ratios 0.78 (1)/0.22 (1), 0.67 (1)/0.33 (1) and 0.58 (1)/0.42 (1).

Silylation[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral ChemistryDecanecyclam010402 general chemistry010403 inorganic & nuclear chemistryCondensed Matter PhysicsBioinformaticsHEXAX-ray crystal structure01 natural sciencesMedicinal chemistry3. Good health0104 chemical scienceslcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999[ CHIM.ORGA ] Chemical Sciences/Organic chemistryCyclamGeneral Materials ScienceDiazobisaminalComputingMilieux_MISCELLANEOUS
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Synthesis and Reactivity of New Complexes of Rhodium and Iridium with Bis(dichloroimidazolylidene) Ligands. Electronic and Catalytic Implications of …

2006

The preparation of a new bis(dichloroimidazolylidene) ligand has provided chelate-N-heterocyclic complexes of Rh(I) and Ir(I), which have been fully characterized. The crystal structures of three of the new complexes are described. The study of the electronic properties of the new ligands was made on the basis of the ν(CO) stretching frequencies of the carbonyl derivatives, showing that the chloroimidazolylidene ligand is significantly less σ-donating than the related nonchlorinated analogue. This electronic modification of the ligand has important implications for the catalytic properties of the compounds obtained, as observed from enhanced activity shown in catalytic hydrosilylation of te…

StereochemistryHydrosilylationLigandOrganic Chemistrychemistry.chemical_elementCrystal structureMedicinal chemistryRhodiumCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryCarbonyl derivativesReactivity (chemistry)IridiumPhysical and Theoretical ChemistryOrganometallics
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Characterization of acrylic resins used for restoration of artworks by pyrolysis-silylation-gas chromatography/mass spectrometry with hexamethyldisil…

2006

A procedure based on the technique of the pyrolysis-GC/MS has been applied, in this work, in order to determine the composition of synthetic acrylic resins employed in artworks. The method is based on the on line derivatization of these resins using hexamethyldisilazane (HMDS). Results obtained have been compared with those others from direct pyrolysis and in situ thermally assisted hydrolysis and methylation with tetramethylammonium hydroxide (TMAH). Sensitivity using HMDS as derivatising reagent is found similar to that from direct pyrolysis and methylation with TMAH. Better resolution of the most representative peaks has been also obtained. Additionally, this method reduces the formation…

Tetramethylammonium hydroxideChromatographyHot TemperatureResolution (mass spectrometry)SilylationOrganic ChemistryVarnishAcrylic ResinsGeneral MedicineBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryvisual_artPaintvisual_art.visual_art_mediumOrganosilicon CompoundsDerivatizationPyrolysisAcrylic resinArtAcrylic acidJournal of chromatography. A
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Analytical characterization of diterpenoid resins present in pictorial varnishes using pyrolysis–gas chromatography–mass spectrometry with on line tr…

2005

Abstract A procedure based on the technique of the pyrolysis–gas chromatography–mass spectrometry (Py–GC–MS) has been applied, in this work, in order to determine the composition of diterpenoid resin employed in art works. The method is based on the on line derivatization of these resins using hexamethyldisilazane (HMDS). Results obtained were compared with those previously reported in literature from Venice turpentine, Strasbourg turpentine, colophony, sandarac and Manila copal using this same method and with those others from in situ thermally assisted hydrolysis and methylation with tetramethylammonium hydroxide (TMAH). Canada balsam, copper resinate and Copaiba balsam have been also ana…

Tetramethylammonium hydroxideChromatographySilylationOrganic ChemistryVarnishSandaracGeneral Medicineengineering.materialSensitivity and SpecificityBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistryPyrolysis–gas chromatography–mass spectrometrychemistry.chemical_compoundchemistryCanada balsamvisual_artPaintengineeringvisual_art.visual_art_mediumOrganic chemistryGas chromatographyDiterpenesDerivatizationJournal of Chromatography A
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Persistent radicals of trivalent tin and lead.

2008

In this report we present synthetic, crystallographic, and new electron paramagnetic resonance (EPR) spectroscopic work that shows that the synthetic route leading to the recently reported, first persistent plumbyl radical *PbEbt3 (Ebt = ethylbis(trimethylsilyl)silyl), that is, the oxidation of the related PbEbt3-anion, was easily extended to the synthesis of other persistent molecular mononuclear radicals of lead and tin. At first, various novel solvates of homoleptic potassium metallates KSnHyp3 (4a), KPbHyp3 (3a), KSnEbt3 (4b), KPbIbt3 (3c), and KSnIbt3 (4c) (Hyp = tris(trimethylsilyl)silyl, Ibt = isopropylbis(trimethylsilyl)silyl), as well as some heteroleptic metallates, such as [Li(OE…

TrisSilylationTrimethylsilylRadicalInorganic chemistrychemistry.chemical_elementMedicinal chemistrylaw.inventionInorganic Chemistrychemistry.chemical_compoundchemistrylawYield (chemistry)Physical and Theoretical ChemistryHomolepticTinElectron paramagnetic resonanceInorganic chemistry
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ChemInform Abstract: Mono(cyclopentadienyl) Complexes of the Rare-Earth Metals

2010

I. Introduction 1953II. Overview of Synthesis, Structure, and Properties 1954A. Synthetic Methods 1954B. Ligands and Structures 1955III. Halo Complexes 1956A. General 1956B. Divalent Halo Complexes 1956C. Trivalent Halo Complexes 1957IV. Chalcogenido Complexes 1958A. General 1958B. Divalent Chalcogenido Complexes 1958C. Trivalent Chalcogenido Complexes 1959V. Pnicogenido Complexes 1960A. General 1960B. Divalent Amido and Phosphido Complexes 1960C. Trivalent Pnicogenido Complexes 19611. Bis(amido) Complexes 19612. Mixed Halo and Chalcogenido Complexes 1962VI. Hydrocarbyl and Silyl Complexes 1963A. General 1963B. Divalent Complexes 19631. Metallacarbaboranes 19632. Bimetallic Naphthalene Comp…

Trischemistry.chemical_classificationchemistry.chemical_compoundchemistrySilylationCyclopentadienyl complexArylPolymer chemistryGeneral MedicineBimetallic stripAlkylNaphthaleneDivalentChemInform
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Bis-organosilane applications and synthesis

2017

Tutkielman kirjallisuusosuudessa perehdytään organofunktionaalisiin silaaneihin. Näitä yhdisteitä käytetään kytkentäaineina komposiittien valmistuksessa sekä monessa muussa sovelluksessa, kuten hydrofobisten ja hydrofiilisten pintojen muodostamiseen, kuivausaineina, ulkoisena elektroniluovuttajana polymeroinnissa, sekä kosteuskovettuvien silaanimodifioitujenpolymeeriliimojen (SMP) kovettumisreaktiossa. Silaanien kosteuskovettuminen johtuu pii-atomiin (Si) sitoutuneiden ryhmien hydrolysoitumisesta kosteuden vaikutuksesta, jolloin syntyy silanoli-ryhmiä (Si-OH), jotka voivat edelleen kondensoitua keskenään muodostaen siloksaanisidoksia (Si-O-Si) tai sidoksia pintojen hydroksyyliryhmien kanssa…

bis-organosilanehydrosilylationaminofunctionalnucleophilic substitution
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1994

The synthesis of linear carbohydrate modified polysiloxanes has been successfully performed by hydrosilation of functionalized and protected carbohydrate derivates. The functionalization (allyl glycosilation) may be applied to a wide variety of reducing carbohydrates. In this study, mono-, di- and oligosaccharides were converted by a simple two-step reaction (β-acetylation and allyl glycosilation) into active compounds, allowing the polymer analogous addition to random poly[dimethyl-co-hydromethyl]siloxanes (hydrosilation). By variation of the Si–H amount in the starting polymers, polysiloxanes with 1.5% to 56% (by weight) carbohydrate content were prepared. At small degrees of substitution…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsChemistryHydrosilylationGeneral Chemical EngineeringDisaccharideChemical modificationPolymerOligosaccharideCarbohydratechemistry.chemical_compoundPolymer chemistryOrganic chemistryMethanolActa Polymerica
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Stereoselektive c-glycosidsynthese durch titan-(iv)-katalysierte addition von silylenolethern an 2-acyloxy-3-keto-glycale

1984

Abstract C-Glycosides are stereoselectively formed by the titan-(IV)-catalysed addition of silyl enolethers 2 to 2,4,6-tri-O-acyl-1-deoxy-D-erythro-hex-1-enopyran-3-uloses 1 followed by elimination of the 4-acyloxy substituent. Cyclohexenyl silylether 2a reacts with 2-acetoxy-3-keto-glycal derivative la forming only one product 3a . Thus, the reaction seems to be diastereospecific with respect to both new chiral centers of the product.

chemistry.chemical_classificationC glycosidesKetoneSilylationGlycalStereochemistryOrganic ChemistrySubstituentBiochemistryCatalysischemistry.chemical_compoundchemistryDrug DiscoveryEnol etherDerivative (chemistry)Tetrahedron Letters
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