Search results for "Aromatic ketones"

showing 3 items of 3 documents

Photochemical Size Reduction of CdSe and CdSe/ZnS Semiconductor Nanoparticles Assisted by nπ* Aromatic Ketones

2009

A novel effect of n pi* aromatic ketones on the quantum dots optical properties is reported. By controlling experimental conditions such as time of irradiation, presence of air in the media, hydrogen donor capacity of the solvent, and irradiation wavelength, core and core-shell CdSe QDs can be resized as convenient.

HydrogenChemistrySize reductionAromatic ketonestechnology industry and agriculturechemistry.chemical_elementGeneral Chemistryequipment and suppliesPhotochemistryBiochemistryCatalysisSolventWavelengthColloid and Surface ChemistryQuantum dotIrradiationSemiconductor NanoparticlesJournal of the American Chemical Society
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Catalytic activity of rare-earth-supported catalysts in Friedel–Crafts acylations

1999

Abstract Friedel–Crafts acylations are catalysed by rare-earth-supported catalysts. The preparation, characterization and performance of these solid catalysts in a test acylation reaction and in a variety of syntheses of aromatic ketones are reported. In contrast to the reactions using AlCl3, the experimental conditions are non-polluting and the final work-up does not require any aqueous treatment.

LanthanideAcylationAqueous solutionChemistryProcess Chemistry and TechnologyAromatic ketonesRare earthOrganic chemistryPhysical and Theoretical ChemistryHeterogeneous catalysisFriedel–Crafts reactionCatalysisCatalysisJournal of Molecular Catalysis A: Chemical
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CO2 as a C1-organic building block: Electrocarboxylation of aromatic ketones. A quantitative study of the effect of the concentration of substrate an…

2006

The purpose of this work is to establish and discuss quantitative relationships between the selectivity in preparative scale electrolysis and intrinsic and operational parameters for the electrocarboxylation of aromatic ketones. For the investigated ketones, under appopriate experimental conditions the selectivity of the process is mainly determined by the competition between carboxylation and protonation, de-halogenation reactions (when an halogenated ketone is involved), and possibly dimerizations involving the electrogenerated radical anion. A simple model was proposed to account for these unwanted side paths which allows to predict the dependence of the selectivity as a function of the …

chemistry.chemical_classificationElectrolysisKetoneGeneral Chemical EngineeringInorganic chemistryProtonationSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryElectrocarboxylation Electrochemistry Aromatic ketonesCarbon dioxide Concentration profileAnalytical Chemistrylaw.inventionchemistry.chemical_compoundchemistryCarboxylationlawElectrochemistryBenzophenoneOrganic chemistrySelectivityAcetophenoneJournal of Electroanalytical Chemistry
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