Search results for "Reinforced carbon–carbon"

showing 5 items of 5 documents

Hydrogenolysis of carbon–carbon σ-bonds using water catalysed by semi-rigid diiridium(iii) porphyrins

2019

Semi-rigid diiridium(III) porphyrin alkyls with m-xylyl and p-xylyl diether linkers were synthesized. They were found to be catalysts for the carbon–carbon σ-bond hydrogenolysis of [2.2]paracyclophane under neutral conditions using water as the hydrogen source. The ether linkages in semi-rigid diiridium(III) porphyrins are unstable and undergo cleavage during the reaction.

HydrogenChemistryReinforced carbon–carbonchemistry.chemical_elementEther02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyCleavage (embryo)01 natural sciencesPorphyrinCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundHydrogenolysisPolymer chemistryMaterials Chemistry0210 nano-technologyNew Journal of Chemistry
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ASSESSMENT OF THE STRENGTH OF CARBON-CARBON COMPOSITES IN CROSS-BENDING AND SHEARING

2015

Shearing (physics)Materials scienceShear (geology)Mechanics of MaterialsUltimate tensile strengthCeramics and CompositesReinforced carbon–carbonComposite materialComposites: Mechanics, Computations, Applications: An International Journal
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Reactivity of the carbon-carbon double bond towards nucleophilic additions. A dft analysis

2004

Abstract The global and local electrophilicity indexes have been used to characterize the reactivity pattern of the CC double bond towards nucleophilic addition reactions. A wide family of molecules including ketones, esters, anhydrides, nitriles and nitrocompounds containing appropriate substitution on the CC double bond have been classified within an unique scale of reactivity. The predictive capability of the theoretical model is tested against a series of benzylidenemalononitriles and substituted α-nitrostilbenes.

chemistry.chemical_classificationNucleophilic additionDouble bondOrganic ChemistryReinforced carbon–carbonBiochemistrychemistryNucleophileComputational chemistryDrug DiscoveryElectrophileOrganic chemistryMoleculeDensity functional theoryReactivity (chemistry)
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The synergy between the CsPbBr3 nanoparticle surface and the organic ligand becomes manifest in a demanding carbon–carbon coupling reaction

2020

We demonstrate here the suitability of CsPbBr3nanoparticles as photosensitizers for a demanding photoredox catalytic homo- and cross-coupling of alkyl bromides at room temperature by merely using visible light and an electron donor, thanks to the cooperative action between the nanoparticle surface and organic capping. Fil: Rosa-Pardo, Ignacio. Instituto de Ciencia Molecular; España. Universidad de Valencia; España Fil: Casadevall, Carla. Barcelona Institute Of Science And Technology. Institut Català D'investigació Química.; España Fil: Schmidt, Luciana Carina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigac…

chemistry.chemical_classificationPEROVSKITE CsPbBr3LigandChemistryMetals and AlloysReinforced carbon–carbonNanoparticleElectron donorGeneral ChemistryPhotochemistryCatalysisCoupling reactionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysis//purl.org/becyt/ford/1 [https]chemistry.chemical_compoundCARBON-CARBON COUPLING//purl.org/becyt/ford/1.4 [https]Materials ChemistryCeramics and CompositesPHOTOREDOXAlkylVisible spectrumChemical Communications
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A new general fragmentation reaction in mass spectrometry: The hydrogen-carbon, carbon-carbon double rearrangement of 2 heteroalkyl substituted diphe…

1995

Diphenylmethyl cations formed by benzylic cleavage of the molecular ions of ortho heteroalkyl substituted 1,1-diphenylalkanes undergo the double rearrangement process (H to C followed by C to C) previously reported for ortho-methoxy derivatives. Hence the formation of substituted benzyl (or tropylium) ions allowing this double rearrangement process constitutes an interesting type of fragmentation reaction characteristic for 1,1-diphenylalkanes bearing ortho substituents (OMe, OEt, OiPr, SMe, NHMe, NMe2) which are able to transfer a hydride to the charged benzyl carbon of diphenylmethyl cations formed by benzylic cleavage of the molecular ion.

inorganic chemicalsCollision-induced dissociationHydrogenChemistryHydrideorganic chemicalsPolyatomic ionReinforced carbon–carbonAnalytical chemistrychemistry.chemical_elementMass spectrometryMedicinal chemistryIonFragmentation (mass spectrometry)heterocyclic compoundsSpectroscopyEuropean Journal of Mass Spectrometry
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