Search results for "carboxylates"

showing 3 items of 13 documents

Imidazolium-2-carboxylate as an afficient, expeditious and eco-friendly organocatalyst for glycerol carbonate synthesis

2009

An improved and greener approach towards the synthesis of glycerol carbonate, via transesterification, using 1-n-butyl-3-methylimidazolium-2-carboxylate as catalyst is described. The catalyst loading as low as 1% was sufficient to yield quantitative conversions. A plausible mechanism is proposed for the catalytic cycle leading to product formation.

glycerol carbonate010405 organic chemistryChemistry[CHIM.CATA]Chemical Sciences/CatalysisGeneral ChemistryTransesterification010402 general chemistry01 natural sciencesEnvironmentally friendly0104 chemical sciencesCatalysistransesterificationchemistry.chemical_compoundimidazolium-2-carboxylates[ CHIM.CATA ] Chemical Sciences/CatalysisCatalytic cycleorganic catalysisdimethyl carbonateGlycerolOrganic chemistryCarbonateCarboxylateDimethyl carbonateComputingMilieux_MISCELLANEOUS
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From 1D coordination polymers to Metal Organic Frameworks by the use of 2-pyridyl oximes.

2020

The synthesis and characterization of coordination polymers and metal&ndash

metal–organic frameworks (MOFs)MagnetismPolymersdetectioncarboxylatesmixed-ligand02 engineering and technology010402 general chemistry01 natural scienceslcsh:TechnologyArticleMetalchemistry.chemical_compoundPolymer chemistryGeneral Materials Sciencelcsh:Microscopylcsh:QC120-168.85chemistry.chemical_classificationMagnetismeFerric oxidelcsh:QH201-278.5Ligandlcsh:TMagnetismPolymer021001 nanoscience & nanotechnologyOximeMagnetic susceptibility0104 chemical sciencesPolímerscoordination polymerschemistrylcsh:TA1-2040magnetismvisual_artvisual_art.visual_art_mediumencapsulationMetal-organic frameworklcsh:Descriptive and experimental mechanicslcsh:Electrical engineering. Electronics. Nuclear engineeringÒxid de ferropyridyl oximes0210 nano-technologySelectivitylcsh:Engineering (General). Civil engineering (General)lcsh:TK1-9971iron(III)
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Carboxylate catalyzed isomerization of β,γ‐unsaturated N-acetylcysteamine thioesters

2022

We demonstrate herein the capacity of simple carboxylate salts – tetrametylammonium and tetramethylguanidinium pivalate – to act as catalysts in the isomerization of β,γ-unsaturated thioesters to α,β-unsaturated thioesters. The carboxylate catalysts gave reaction rates comparable to those obtained with DBU, but with fewer side reactions. The reaction exhibits a normal secondary kinetic isotope effect ( k 1H / k 1D = 1.065±0.026) with a β,γ−deuterated substrate. Computational analysis of the mechanism provides a similar value ( k 1H / k 1D = 1.05) with a mechanism where γ-reprotonation of the enolate intermediate is rate determining. peerReviewed

thioesterskatalyytitkinetic isotope effectsisomeriakatalyysirikkiyhdisteetcarboxylatesreaction mechanismreaktiomekanismitbase catalysisisomerizationenolatesorgaaniset yhdisteet
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