Search results for "Reaction condition"

showing 10 items of 70 documents

Dissolution and hydrolysis of fibre sludge using hydroxyalkylimidazolium hydrogensulphate ionic liquids

2014

Abstract The dissolution and hydrolysis of wet fibre sludge in ionic liquids (ILs) with different reaction conditions are performed in this study. Novel types of hydroxyalkylimidazolium hydrogensulphate ILs, [glymim]HSO 4 , [hemim]HSO 4 and [hpmim]HSO 4 , are especially designed and aimed to combine the dissolution and hydrolysis of wet fibre sludge in a one-step pretreatment. The results were obtained based on the analysis of total reducing sugars (TRS) with the DNS method. The dissolution and hydrolysis of fresh wild horse chestnut fruit ( Aesculus hippocastanum ) with the same ILs were also carried out as a comparison reference. Since fibre sludge is cellulose based and horse chestnut fr…

Aesculus hippocastanumReaction conditionsChromatographyRenewable Energy Sustainability and the EnvironmentStarchForestryHorse chestnutchemistry.chemical_compoundHydrolysischemistryIonic liquidta219CelluloseWaste Management and DisposalAgronomy and Crop ScienceDissolutionta116Biomass and Bioenergy
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A Combination of Visible-Light Organophotoredox Catalysis and Asymmetric Organocatalysis for the Enantioselective Mannich Reaction of Dihydroquinoxal…

2019

[EN] An enantioselective photooxidative Mannich reaction of dihydroquinoxalinones with ketones by the merger of organophotoredox and asymmetric organocatalysis is described. This protocol features very mild reaction conditions using simple and cheap catalysts (Eosin Y and (S)-Proline) for the synthesis of chiral quinoxaline derivatives with good to high yields (up to 94%) and excellent enantioselectivities (up to 99% ee).

AlkylationActivation010402 general chemistry01 natural sciencesBiochemistryCatalysisReaccions químiqueschemistry.chemical_compoundQuinoxalineCatàlisiComplexesTertiary-AminesAcidOrganic chemistryPhysical and Theoretical ChemistryEosin YFunctionalizationMannich reactionReaction conditions010405 organic chemistryOrganic ChemistryEnantioselective synthesisMethodology0104 chemical sciencesPhotoredox catalysisEfficientchemistryOrganocatalysisFISICA APLICADAHydrogenationQuímica orgànicaVisible spectrum
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Regio-specific synthesis of new 1-(tert-butyl)-1H-pyrazolecarboxamide derivatives

2017

Regio-specific and non-regiospecific condensation reactions on 1,3-dicarbonyl compounds rendered 1,3,5-trisubstituted pyrazoles. Herein, the control of regio-specificity was a significant improvement in pyrazole research. A high yield acylation of poorly nucleophilic aryl amines, which resulted in mono- or diacylated products depending on the reaction conditions, is described. As a result, a library of potentially bioactive compounds was obtained. Fil: Ruatta Merke, Santiago Matías. Universidad Nacional del Litoral. Facultad de Bioquímica y Ciencias Biológicas; Argentina Fil: Murguia, Marcelo Cesar. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Co…

Arylamine acylationRegio-specific condensationPyrazole010402 general chemistry01 natural sciencesBiochemistryAcylationchemistry.chemical_compoundNucleophileDrug DiscoveryOrganic chemistryTert butylReaction conditions010405 organic chemistryChemistryArylOtras Ciencias Químicastert-Butyl hydrazineOrganic ChemistryCiencias QuímicasPyrazole carboxamideCondensation reaction0104 chemical sciencesDiacylationYield (chemistry)CIENCIAS NATURALES Y EXACTAS
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Untersuchungen zur Diastereoselektivität beim O ‐Angriff von Elektrophilen auf β‐Ketocarbonsäureester‐Enolate

1989

Aus den in reiner Form eingesetzten Z- oder E-Enolen 2a–c werden uber die Enolatstufe 3a–c die O-alkylierten, -silylierten oder -acylierten Produkte 4aa–ae, 4ba, bf und 4ca, cc, cf hergestellt. Im Gegensatz zu der vollstandigen Regioselektivitat hangt die Z/E-Diastereoselektivitat dabei von den Substituenten in 2/3, dem verwendeten Elektrophil und den Reaktionsbedingungen ab. Insbesondere bei weichen Elektrophilen kann sich das Z/E-Verhaltnis bei der Umsetzung 34 stark andern. On the Diastereoselectivity of the O-Attack of Electrophiles on Enolates from β-Ketocarboxylates The O-alkylated, -silylated or -acylated derivatives 4aa–ae, 4ba, bf, 4ca, cc, cf of the pure Z or E enoles 2a–c are gen…

Inorganic ChemistryReaction conditionschemistry.chemical_classificationStereochemistryChemistryElectrophileEnol etherRegioselectivityAliphatic compoundChemische Berichte
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Photochemie des 1,3,5‐Tristyrylbenzols

1984

In Abhangigkeit von den Reaktionsbedingungen erhalt man bei der Belichtung der Titelverbindung 1 das Cyclophan 5, das Pyrenderivat 6 oder das polykondensierte aromatische System 9. Fur den neuen Cyclophantyp 5, bei dem zwei Benzolringe selbst wieder durch Ringe verbruckt sind, wurde eine Rontgenstrukturanalyse durchgefuhrt. Photochemistry of 1,3,5-Tristyrylbenzene Depending on the reaction conditions the irradiation of the title compound 1 yields the cyclophane 5, the pyrene derivative 6, or the polycondensed aromatic system 9. An X-ray analysis was performed for 5, representing a new type of cyclophane in which two benzene rings are bridged again by rings.

Inorganic ChemistryReaction conditionschemistry.chemical_classificationchemistry.chemical_compoundPolycyclic compoundStereochemistryChemistryPyreneMedicinal chemistryDerivative (chemistry)CyclophaneChemische Berichte
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Synthesen mit substituierten Malondialdehyden, XI. γ‐Formyl‐tetramethinmerocyanin‐, γ‐Formyl‐pentamethincyanin‐ und [2.2.2]Heptamethincyanin‐Farbstof…

1972

Durch Kondensation des Formylmalondialdehyds (Triformylmethan) 5 mit heterocyclischen Imoniumsalzen 4 werden je nach Reaktionsbedingungen neuartige γ-Formyl-tetramethinmerocyanin-(6), γ-Formyl-pentamethincyanin-(8) und trinucleare symmetrische [2.2.2]Heptamethincyanin-Farbstoffe (9) dargestellt. Die Isolierung der Mono- (6) und Dikondensationsprodukte (8) des Formylmalondialdehyds ermoglicht die Darstellung unsymmetrischer Farbstoffe 8 und 9 mit verschiedenen Endgruppen. — Die trinuclearen [2.2.2]Heptamethincyanine 9 lassen sich in Analogie zu den phenylogen Guanidiniumionen (Triphenylmethanfarbstoffe) als methinyloge Guanidiniumkationen 3 (n = 3) auffassen. — Die spektroskopischen Eigensch…

Inorganic ChemistryReaction conditionschemistry.chemical_compoundTriphenylmethaneChemistryStereochemistrySpectral propertiesMedicinal chemistryTriformylmethaneChemische Berichte
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Direct formation of Sub-Micron and Nanoparticles of a bioinspired coordination polymer based on Copper with Adenine

2017

We report on the use of different reaction conditions, e.g., temperature, time, and/or concentration of reactants, to gain control over the particle formation of a bioinspired coordination polymer based on copper(II) and adenine, allowing homogeneous particle production from microto submicro-, and up to nano-size. Additionally, studies on this reaction carried out in the presence of different surfactants gives rise to the control of the particle size due to the modulation of the electrostatic interactions. Stability of the water suspensions obtained within the time and pH has been evaluated. We have also studied that there is no significant effect of the size reduction in the magnetic prope…

Materials sciencePolymers and PlasticsCoordination polymerSurfactantsInorganic chemistryNanoparticlechemistry.chemical_element010402 general chemistry01 natural sciencesArticlesurfactantslcsh:QD241-441coordination polymers; surfactants; nanoparticleschemistry.chemical_compoundlcsh:Organic chemistryReaction conditions010405 organic chemistryGeneral ChemistryQuímicaElectrostaticsCopper0104 chemical sciencesCoordination polymerscoordination polymerschemistryHomogeneousParticleNanoparticlesnanoparticlesParticle size
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The rate of polymerization in two loci reaction systems: VDF-HFP precipitation copolymerization in supercritical carbon dioxide

2011

When the copolymerization of vinylidene fluoride (VDF) and hexafluoropropylene (HFP) is carried out in supercritical carbon dioxide (scCO 2) under heterogeneous conditions, the reaction occurs both in the continuous CO 2-rich phase and in the dispersed polymer-rich phase. The two phases being characterized by different values of reactant concentrations and kinetic parameters, one would expect that the reaction kinetics is affected by the polymer phase holdup in the reactor. However, the reaction rate is almost insensitive to the amount of produced polymer, at least at specific reaction conditions. This apparent contradiction is discussed and clarified in this paper by a series of comparativ…

Materials sciencePolymers and PlasticsRich phaseChemical kineticsReaction ratechemistry.chemical_compoundSupercritical carbon dioxideCopolymerCopolymerizationPhase (matter)Single phasePolymer chemistryMaterials ChemistryCopolymerHeterogeneous conditionPolymerRate of polymerizationReaction systemchemistry.chemical_classificationSupercritical carbon dioxideHexafluoropropyleneExperimental investigationComparative simulationGeneral ChemistryPolymerComputer simulationReaction rates Supercritical fluid extractionReactant concentrationchemistryPolymerizationChemical engineeringReaction conditionVinylidene fluoride Carbon dioxideHeterogeneous polymerizationHexafluoropropylenePolymer phasePolymer Engineering & Science
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Biomimetic chitosan-mediated synthesis in heterogeneous phase of bulk and mesoporous silica nanoparticles

2009

Both bulk and mesoporous silica nanoparticles can be obtained in the form of granular aggregates using chitosan flakes as additive under very soft biomimetic reaction conditions. Puchol Estors, Victoria, Victoria.Puchol@uv.es ; El Haskouri, Jamal, Jamal.Haskouri@uv.es ; Latorre Saborit, Julio, Julio.Latorre@uv.es ; Beltran Porter, Aurelio, Aurelio.Beltran@uv.es ; Beltran Porter, Daniel, Daniel.Beltran@uv.es ; Amoros del Toro, Pedro Jose, Pedro.Amoros@uv.es

Materials scienceSilicon dioxideUNESCO::QUÍMICANanoparticleNanotechnologyBulk:QUÍMICA [UNESCO]CatalysisChitosanchemistry.chemical_compoundMicroscopy Electron TransmissionBiomimeticsPhase (matter)Materials ChemistryReaction conditionsChitosanUNESCO::QUÍMICA::Química inorgánicaMesoporus silicaMetals and AlloysGeneral ChemistryMesoporous silica:QUÍMICA::Química inorgánica [UNESCO]Silicon DioxideSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryMicroscopy Electron ScanningCeramics and CompositesNanoparticlesBiomimeticBulk ; Mesoporus silica ; Biomimetic ; Nanoparticles ; ChitosanChemical Communications
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Alkylation of Benzene with Short-Chain Olefins over MCM-22 Zeolite: Catalytic Behaviour and Kinetic Mechanism

2000

Abstract Benzene alkylation with ethene and propene has been carried out under liquid-phase reaction conditions over zeolites MCM-22, Beta, and ZSM-5. MCM-22 seems to be a good catalyst for benzene alkylation especially with propene, showing high activity and stability and good selectivity. Kinetic experiments show that alkylation with propene follows an Eley–Rideal type mechanism.

PropeneReaction conditionschemistry.chemical_compoundchemistryPhysical and Theoretical ChemistryAlkylationSelectivityZeoliteKinetic energyPhotochemistryBenzeneCatalysisCatalysisJournal of Catalysis
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