Search results for "dehalogenation"

showing 2 items of 2 documents

Polycyclic aromatic chains on metals and insulating layers by repetitive [3+2] cycloadditions

2020

The vast potential of organic materials for electronic, optoelectronic and spintronic devices entails substantial interest in the fabrication of π-conjugated systems with tailored functionality directly at insulating interfaces. On-surface fabrication of such materials on non-metal surfaces remains to be demonstrated with high yield and selectivity. Here we present the synthesis of polyaromatic chains on metallic substrates, insulating layers, and in the solid state. Scanning probe microscopy shows the formation of azaullazine repeating units on Au(111), Ag(111), and h-BN/Cu(111), stemming from intermolecular homo-coupling via cycloaddition reactions of CN-substituted polycyclic aromatic az…

Materials scienceFabricationScienceGeneral Physics and Astronomy02 engineering and technologyConjugated system010402 general chemistry01 natural sciencesArticleGeneral Biochemistry Genetics and Molecular Biologylaw.inventionchemistry.chemical_compoundScanning probe microscopylawDehydrogenationon-surface synthesislcsh:Science13-dipolar cycloadditionschemistry.chemical_classificationMultidisciplinaryalgorithmGrapheneQgrapheneazomethine ylidesGeneral ChemistryPolymer021001 nanoscience & nanotechnologyCycloadditionddc:0104 chemical sciencesCU(111)total-energy calculationschemistryChemical engineeringboron-nitrideBoron nitrideazide-alkyne cycloadditionlcsh:QMaterials chemistrydehalogenation0210 nano-technology
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Influence of the nature of the substrate and of operative parameters in the electrocarboxylation of halogenated acetophenones and benzophenones

2005

Abstract The electrocarboxylation of halogenated acetophenones and benzophenones to the corresponding hydroxycarboxylic acids has been carried out in undivided cell equipped with aluminium sacrificial anode and using 1-methyl-2-pyrrolidinone (NMP) as the solvent. The radical anion generated by the electro-reduction of the aromatic ketone is involved in several competitive reactions which lead to the formation of the target hydroxycarboxylic acid, the corresponding alcohol and pinacol and the de-halogenated parent ketone. If sufficiently negative working potentials are imposed, the latter is reduced to the corresponding carboxylate, pinacol and alcohol. Very different results in terms of sel…

chemistry.chemical_classificationKetonePinacolGeneral Chemical EngineeringCarboxylic acidHalogenationReductive dehalogenationAlcoholSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrocarboxylationchemistry.chemical_compoundchemistryCarboxylationRadical anionsHalobenzophenoneElectrochemistryOrganic chemistryHaloacetophenoneCarboxylateSelectivity
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