Search results for "Nagel"

showing 5 items of 25 documents

ChemInform Abstract: Sequential Suzuki/Asymmetric Aldol and Suzuki/Knoevenagel Reactions under Aqueous Conditions.

2012

Here we describe for the first time a sequential Suzuki/asymmetric aldol reaction. Such sequential approach was achieved through the combined use of an ionic liquid supported palladium catalyst and the organocatalyst trans-4-(2,2-diphenylacetoxy)proline. Suzuki and asymmetric aldol reactions were performed under aqueous conditions. The use of a palladium catalyst under basic conditions allowed also the first example of sequential Suzuki/Knoevenagel reaction. Reactions were carried out under aqueous conditions and products were isolated in good to high yields and, in the case of the Suzuki/aldol reaction, with diastereoselectivities up to 91:9 and enantioselectivities up to at least 99 %.

chemistry.chemical_compoundAddition reactionAqueous solutionchemistryAldol reactionCombined useIonic liquidOrganic chemistryKnoevenagel condensationGeneral MedicinePalladium catalystChemInform
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Nanoparticle-Directed Metal–Organic Framework/Porous Organic Polymer Monolithic Supports for Flow-Based Applications

2017

A two-step nanoparticle-directed route for the preparation of macroporous polymer monoliths for which the pore surface is covered with a metal–organic framework (MOF) coating has been developed to facilitate the use of MOFs in flow-based applications. The flow-through monolithic matrix was prepared in a column format from a polymerization mixture containing ZnO-nanoparticles. These nanoparticles embedded in the precursor monolith were converted to MOF coatings via the dissolution–precipitation equilibrium after filling the pores of the monolith with a solution of the organic linker. Pore surface coverage with the microporous zeolitic imidazolate framework ZIF-8 resulted in an increase in su…

geographyMaterials sciencegeography.geographical_feature_category02 engineering and technologyMicroporous materialengineering.material010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCoatingPolymerizationChemical engineeringengineeringOrganic chemistryGeneral Materials ScienceKnoevenagel condensationMetal-organic frameworkMicroreactorMonolith0210 nano-technologyZeolitic imidazolate frameworkACS Applied Materials & Interfaces
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Catalytic activity of humic substances in condensation reactions

1998

Abstract Humic substances (HS) have considerable impact on the fate of organic xenobiotics in natural environments. This paper reports on the catalytic activity of HS in condensation reactions of carbonyl compounds with active methylene compounds, using Knoevenagel and Claisen-Schmidt reactions as examples. Of the HS, the aquatic fulvic acids are the most active, but the velocity of condensation reactions depends also on the temperature, concentration and form of HS (free or salt) used, and the solvent.

lcsh:GE1-350chemistry.chemical_classificationChemistryMineralogySalt (chemistry)Condensation reactionCatalysisSolventchemistry.chemical_compoundOrganic chemistryKnoevenagel condensationMethyleneXenobioticlcsh:Environmental sciencesGeneral Environmental ScienceEnvironment International
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Solvatochromic behaviour of new donor–acceptor oligothiophenes

2021

Oligothiophene derivatives play a central role in the formulation of materials used in devices in the field of organic electronics. In this work, we report the results of the study of UV-vis absorption and fluorescence spectra, in several solvents, of a series of oligothiophenes recently synthesized in our laboratory. The studied oligothiophenes present different structures due to several factors: the donor– acceptor (D–A) or acceptor–donor–acceptor (A–D–A) architecture, the number of thiophene rings in the backbone (ranging from three to eight), the number and position of solubilizing octyl chains in the backbone, and the type of acceptor moieties (from Knoevenagel condensation either with…

oligothiophenessolvatochromism02 engineering and technology010402 general chemistryElectrochemistryPhotochemistry01 natural sciencesCatalysischemistry.chemical_compoundMaterials ChemistryThiopheneOrganic electronicsanodic dimerizationSolvatochromismSettore CHIM/06 - Chimica OrganicaGeneral Chemistry021001 nanoscience & nanotechnologyAcceptor0104 chemical scienceschemistryoligothiophenes; solvatochromism; anodic dimerizationKnoevenagel condensationAbsorption (chemistry)0210 nano-technologyDonor acceptorOligothiophenes fluorescence donor-acceptor systemsNew Journal of Chemistry
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Synthesis, Structure and Solvatochromism of the Emission of Cyano-Substituted Oligo(phenylenevinylene)s

2001

Strongly luminescent and highly soluble oligo(phenylenevinylene)s with five benzene rings and cyano groups in different positions of the terminal styrene units were prepared by means of Horner and Knoevenagel reactions. The substitution pattern − cyanide moieties on the vinyl or on the aromatic regions, together with the effect of auxochromic groups − has distinct influences on the electronic spectra, particularly on the fluorescence. Polar solvents induce red shifts and strongly reduce the fluorescence intensity of the vinyl-substituted oligomers. Cyano substitution increases the electron affinity of the oligomers; this effect is more pronounced for molecules with vinyl cyanides and can be…

organic chemicalsOrganic ChemistrySolvatochromismPhotochemistryOligomerStyrenechemistry.chemical_compoundBenzonitrilechemistryElectron affinity (data page)Polymer chemistryMoleculeKnoevenagel condensationPhysical and Theoretical ChemistryBenzeneEuropean Journal of Organic Chemistry
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