Search results for " carboxylation"

showing 3 items of 3 documents

Unravelling Radicals Reactivity Towards Carbon Nanotubes Manipulation/Functionalization

2016

Carbon Nanotubes (CNTs) chemistry is under constant evolution, as a consequence of the deep interest of the scientific community in finding new applications for these versatile materials. New and old synthetic protocols are used for improving the control of the functionalization degree of the final materials and for offering to scientists the possibility to fine-tune their final properties. In this Review, we focus the attention on radical reactions, a class of protocols characterized by small number of steps, different degrees of functionalization and enhanced solubility of the final modified CNTs, in the desired environment. The most well-known protocols are analysed providing some releva…

Radical02 engineering and technologyCarbon nanotube010402 general chemistryPhotochemistry01 natural sciencesCarbon nanotubelaw.inventioncarboxylationBirch reductionlawepoxidationOrganic chemistryReactivity (chemistry)diazonium saltsradicalBirch reductionChemistryOrganic Chemistry021001 nanoscience & nanotechnologyradicals0104 chemical sciencesCarboxylationdiazonium saltSurface modificationCarbon Nanotubespolymer grafting0210 nano-technologyCarbon Nanotubes radicals carboxylation diazonium salts Birch reduction epoxidation polymer grafting
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Electrocarboxylation of Benzyl Halides through Redox Catalysis on the Preparative Scale

2006

The electrocarboxylation of benzyl halides to the corresponding carboxylic acids through homogeneous charge-transfer catalysis was investigated both theoretically and experimentally to determine the influence of the operative parameters on the yield of the process and on the catalyst consumption. Theoretical considerations, based on fast kinetics of redox catalysis, were confirmed by the electrocarboxylation of 1-phenyl-1-chloroethane catalyzed by 1,3-benzenedicarboxylic acid di methyl ester performed at a carbon cathode under different operative conditions. We obtained high yields of the target carboxylic acid and experienced a low catalyst consumption by operating with optimized [RX]bulk/…

chemistry.chemical_classification010405 organic chemistryChemistryCarboxylic acidOrganic ChemistryInorganic chemistryHalideHomogeneous catalysisGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryElectrochemistry01 natural sciencesRedoxCatalysis0104 chemical sciencesCatalysisCarboxylationYield (chemistry)benzyl halides • carbon dioxide • carboxylation • electrochemistry • homogeneous catalysisComputingMilieux_MISCELLANEOUS
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An unexpected ring carboxylation in the electrocarboxylation of aromatic ketones

2006

The electrocarboxylation of various aromatic ketones, carried out in N-methyl-2-pyrrolidone (NMP) in a diaphragmless cell equipped with a carbon cathode and an aluminium sacrificial anode, yielded, among the products, the target hydroxy acids, the corresponding alcohols and pinacols and, quite surprisingly, detectable amounts of substituted benzoic acids and cycloexene carboxylic acids. These compounds arise from a never reported before electrocarboxylation on the aromatic ring, respectively, for substitution of an aromatic hydrogen and from an addition reaction. For example, the electrocarboxylation of acetophenone gave rise to the substituted benzoic acids in ortho, para and meta position…

inorganic chemicalschemistry.chemical_classificationAddition reactionKetoneorganic chemicalsGeneral Chemical EngineeringReaction intermediateSettore ING-IND/27 - Chimica Industriale E TecnologicaHydrogen atom abstractionchemistry.chemical_compoundMeta-chemistryCarboxylationElectrochemistryOrganic chemistryElectrocarboxylationRing carboxylationKetonesCarbon dioxideUndivided cellsBenzoic acidAcetophenone
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