Search results for "nitrile"

showing 10 items of 1539 documents

Oxidative halogenation of substituted pyrroles with Cu(II). PartIII. Bromination and chlorination of 2-benzoylpyrrole

1992

The bromination of 2-benzoylpyrrole with copper(II) bromide in the homogeneous and the heterogeneous phase is described, giving 4- and 5-monobromo derivatives whose ratio decreases as the temperature is increased. The same reaction with copper(II) chloride in acetonitrile at 60° produces 5-chloro-2-benzoylpyrrole as the major product. 4,5-Dihalopyrroles in good yields are obtained with an excess of halogenating agent.

chemistry.chemical_classificationKetoneChemistryOrganic ChemistryHalogenationchemistry.chemical_elementOxidative phosphorylationMedicinal chemistryChlorideCopperchemistry.chemical_compoundBromidePhase (matter)medicineOrganic chemistryAcetonitrilemedicine.drugJournal of Heterocyclic Chemistry
researchProduct

Rare Earth Half-Sandwich Catalysts for the Homo- and Copolymerization of Ethylene and Styrene

2001

The synthesis of rare earth metal half-sandwich hydrido complexes [Ln(η5:η1-C5Me4SiMe2NCMe3)(THF)(μ-H)]2(Ln = Y, Lu, Yb, Er, Tb) through σ-bond metathesis of the alkyl complexes [Ln(η5:η1- C5Me4SiMe2NCMe3)(CH2SiMe3)(THF)], easily accessible by the reaction of the amino-cyclopentadiene with [Ln(CH2SiMe3)3(THF)2], was developed. The dimeric lanthanide hydrido complexes are highly fluxional involving THF dissociation and cis-trans isomerization of the linked amidocyclopentadienyl ligand. The presence of a monomer-dimer equilibrium is suggested by cross-over experiments. They were tested as single-site, single-component catalysts for the polymerization of ethylene, α-olefin, and styrene, as wel…

chemistry.chemical_classificationLanthanidechemistry.chemical_compoundAcrylateEthyleneMaterials sciencePolymerizationchemistryPolymer chemistryCopolymerAcrylonitrileAlkylStyrene
researchProduct

Lauroyl peroxide as thermal initiator of lauryl methacrylate monolithic columns for CEC

2008

The preparation of lauryl methacrylate (LMA)-based monolithic columns for CEC using lauroyl peroxide (LPO) as thermal initiator of polymerization has been investigated. The influence of initiator amount and composition of porogenic solvent on the physical and electrochromatographic properties of the resulting LMA-based monoliths was evaluated. A comparison with LMA-based columns thermally polymerized with AIBN was performed. At a given porogenic solvent composition, LMA stationary phases initiated with LPO showed higher permeabilities and better efficiency values than those prepared using AIBN as initiator. The optimum polymerization mixture found for LPO initiator provided a minimum plate …

chemistry.chemical_classificationLipid PeroxidesChromatographyFree RadicalsPolymersChemistryClinical BiochemistryTemperatureLauric AcidsPolycyclic aromatic hydrocarbonRepeatabilityLauroyl peroxideBiochemistryAnalytical ChemistrySolventPolymerizationCapillary ElectrochromatographyNitrilesThermalMethacrylatesSolvent compositionLauryl methacrylateNuclear chemistryELECTROPHORESIS
researchProduct

Light emitting and electrical properties of pure amorphous thin films of organic compounds containing 2-tert-butyl-6-methyl-4H-pyran-4-ylidene

2013

Abstract Low molecular weight organic compounds which make thin films from organic solutions would be a great benefit in future organic light emitting systems. Two most important advantages should be mentioned. First – repeatability of synthesis of small molecules is better than of polymers. Second – wet casting methods can be applied. In this paper we present optical and opto-electrical properties of three glassy forming compounds containing 2-tert-butyl-6-methyl-4H-pyran-4-ylidene fragment as a backbone. They have the same N,N-dialkylamino electron donating group with attached bulky trityloxyethyl groups. The difference between these compounds is in an electron acceptor group. One has ind…

chemistry.chemical_classificationMaterials scienceBarbituric acidOrganic ChemistryElectron acceptorElectroluminescencePhotochemistryAcceptorOrganic compoundAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsAmorphous solidInorganic Chemistrychemistry.chemical_compoundchemistryPEDOT:PSSElectrical and Electronic EngineeringPhysical and Theoretical ChemistrySpectroscopyMalononitrileOptical Materials
researchProduct

Einfluss des polymerrückgrats auf eigenschaften von thermoplastischen elastomeren

1992

4-Urazoyl benzoic acid groups were statistically attached to various hydrocarbon elastomers, polar elastomers and partially crystalline polymers via a polymer-analogous reaction. DSC, FTIR, stress-strain experiments and dynamic-mechanical analysis were used to analyse whether these systems, analogous to functionalized polybutadienes, would form ordered supra-molecular structures of the polar side-groups that would lead to a thermoreversible crosslinking. While the structure formation is suppressed for elastomers with a large cross-sectional area of the chain (e.g. butyl rubber) or polar side-groups, (e.g. polychloroprene), the mechanical propertie can be controlled by balancing supermolecul…

chemistry.chemical_classificationMaterials scienceButyl rubberPolymerElastomerlaw.inventionchemistry.chemical_compoundNatural rubberchemistrylawvisual_artPolymer chemistryvisual_art.visual_art_mediumGeneral Materials ScienceThermoplastic elastomerCrystallizationNitrile rubberBenzoic acidAngewandte Makromolekulare Chemie
researchProduct

Dicyanobenzothiadiazole Derivatives Possessing Switchable Dielectric Permittivities

2017

Benzothiadiazoles are important electron acceptors and are frequently employed as electron-deficient components of donor-acceptor polymers. We report the effect of nitrile functionalities on the reactivity, steric hindrance, optoelectronic properties, and dielectric permittivity in dicyanobenzothioadiazole (DCNBT). Dielectric spectroscopy in the bulk and in solution assisted by DFT-calculations revealed that these molecules can be engineered to engender maximum values of the dipole moment and of dielectric permittivity due to the strong electron-withdrawing effect of the nitrile groups. The self-assembly in the bulk was investigated by X-ray scattering performed on single crystals, fibers (…

chemistry.chemical_classificationMaterials scienceNitrileRelative permittivity02 engineering and technologyPolymerDielectric010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesDielectric spectroscopyDipolechemistry.chemical_compoundchemistryChemical physicsLiquid crystalPhase (matter)Organic chemistryGeneral Materials Science0210 nano-technologyACS Applied Materials & Interfaces
researchProduct

P-chirogenic organocatalysts: application to the aza-Morita–Baylis–Hillman (aza-MBH) reaction of ketimines

2013

The P-chirogenic organocatalysts were found to promote the enantioselective aza-Morita-Baylis-Hillman reaction of ketimines derived from acyclic α-keto esters. In the P-chirogenic organocatalyzed aza-MBH reactions, α,α-disubstituted α-amino acid derivatives were obtained in high yields with high enantioselectivities (up to 97% ee).

chemistry.chemical_classificationMetals and AlloysEnantioselective synthesisStereoisomerismStereoisomerismGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisAmino acidchemistryNitrilesMaterials ChemistryCeramics and CompositesOrganic chemistryIminesAmino AcidsChemical Communications
researchProduct

Synthesis of novel isoxazoline-fused cispentacin stereoisomers

2009

Abstract New isoxazoline-fused cispentacins were prepared by the 1,3-dipolar cycloaddition of nitrile oxides to β-amino esters containing a cyclopentene skeleton. This synthetic procedure gave regio- and diastereoisomers of the cispentacins. The synthetic route was extended to the synthesis of these compounds in enantiomerically pure form.

chemistry.chemical_classificationNitrileBicyclic moleculeStereochemistryOrganic ChemistryDiastereomerCispentacinBiochemistryCycloadditionAmino acidchemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryCyclopenteneTetrahedron Letters
researchProduct

Selective nitrile oxide dipolar cycloaddition for the synthesis of highly functionalized β-aminocyclohexanecarboxylate stereoisomers

2012

Highly functionalized β-aminocyclohexanecarboxylate regio- and stereoisomers were synthesized from a bicyclic β-lactam by successive regioselective iodolactonization, stereo- and regioselective nitrile oxide cycloaddition, lactone ring-opening and isoxazoline ring-opening.

chemistry.chemical_classificationNitrileBicyclic moleculeStereochemistryOrganic ChemistryOxideIodolactonizationRegioselectivityBiochemistryCycloadditionchemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryta116LactoneTetrahedron
researchProduct

On the Unique Reactivity of Pd(OAc)2with Organic Azides: Expedient Synthesis of Nitriles and Imines

2013

Organic azides are well-established as versatile compounds that can act as precursors of different heterocycles (triazoles, triazolines, tetrazoles, etc.) or other nitrogen-containing compounds, such as amines (Staudinger reduction, Curtius rearrangement) or imines (Schmidt rearrangement, aza-Wittig reaction).1 Besides the ubiquitous copper-catalysed azide–alkyne cycloaddition reaction,2 two applications of organic azides have recently attracted the interest of the synthetic community: 1) the preparation of aziridines through the generation of nitrenes3 and 2) the synthesis of nitriles. We were particularly interested in the latter application, owing to the importance of the cyano group in …

chemistry.chemical_classificationNitrileChemistryOrganic ChemistryImineAlkyneCyanationCatalysisCycloadditionInorganic Chemistrychemistry.chemical_compoundBenzonitrileOrganic chemistryOrganic synthesisAzidePhysical and Theoretical ChemistryChemCatChem
researchProduct