Search results for "Reactivity"

showing 10 items of 880 documents

Site-selectivity control in hetero-Diels-Alder reactions of methylidene derivatives of lawsone through modification of the reactive carbonyl group: a…

2019

A new perspective on the reactivity of hydroxyquinones was revealed as an acetal derivative of lawsone was synthesized, isolated, and used in tandem Knoevenagel/hetero-Diels-Alder reactions catalyzed by S-proline. The intermediate alkylidene-1,3-diones that were formed in situ reacted with electron rich alkenes to predominantly afford pyrano-1,2-naphthoquinone (β-lapachone) derivatives along with the isomeric pyrano-1,4-naphthoquinone (α-lapachone) derivatives in high to excellent total yields. Interestingly, the highly reactive arylidene-1,3-dione derivatives were found to be stable and isolable. DFT calculations suggest that these hetero-Diels-Alder reactions have a high polar character, …

Tandem010405 organic chemistryChemistrySite selectivityOrganic ChemistryAcetal010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistry0104 chemical sciencesCatalysisLawsonechemistry.chemical_compoundDerivative (finance)Knoevenagel condensationReactivity (chemistry)Physical and Theoretical ChemistryOrganicbiomolecular chemistry
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ChemInform Abstract: Synthesis and Reactivity of New β-Enamino Acid Derivatives: A Simple and General Approach to β-Enamino Esters and Thioesters.

2010

A new strategy has been developed for the synthesis of several β-enamino acid derivatives. N,N‘-Carbonyldiimidazole has been used as C-acylating agent of methyl ketimines, providing a direct and simple route to new β-enamino carbonyl imidazole derivatives 2. These derivatives 2 were cleanly and efficiently transformed into β-enamino esters 4 (X = O) and thioesters 4 (X = S) by reaction with a great variety of alcohols and thiols, including tertiary ones. Alternative and complementary routes to compounds 4 were also investigated. In addition, β-keto esters 6 have been obtained by mild acid hydrolysis of β-enamino esters 4.

Terpenechemistry.chemical_compoundchemistryImidazoleOrganic chemistryReactivity (chemistry)Acid hydrolysisGeneral MedicineChemInform
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Ionic liquid binary mixtures: How different factors contribute to determine their effect on the reactivity

2016

We studied how mixing ionic liquids affected the rate of the Diels Alder reaction between 9-anthracenemethanol and N-ethylmaleimide. The mixtures considered spanned the whole compositional range and differed for the anion or the cation. These comprised mixtures of the ionic liquid 1-benzyl-3-butyl-imidazolium bis-(trifluoromethanesulfonyl)imide ([Bzbim][NTf2]) with 1-(2,3,4,5,6-pentafluorophenyl)-3-butyl-imidazolium bis-(trifluoromethanesulfonyl)imide ([Bz(F5)bim][NTf2]) or 1-benzyl-3-butyl-imidazolium tetrafluoroborate ([Bzbim][BF4]). Moreover we studied the reaction in a set of mixtures containing an aliphatic and an aromatic cation, namely [Bzbim+] and N-butyltriethylammonium ([bEt3N+]) …

TetrafluoroborateGeneral Chemical EngineeringInorganic chemistrySolvatochromismfungiionic liquids binary mixtures Diels-Alder reaction02 engineering and technologyGeneral ChemistrySettore CHIM/06 - Chimica Organica010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesSolventchemistry.chemical_compoundchemistryIonic liquidProton NMRPhysical chemistryReactivity (chemistry)0210 nano-technologyImideDiels–Alder reaction
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Reactivity of cellulose during hydrothermal carbonization of lignocellulosic biomass

2020

Abstract Hydrothermal carbonization (HTC) of pure cellulose (CE) and birchwood (BW) samples was carried out at temperatures between 160 and 280 °C, 0.5 h residence time and biomass-to-water ratio 1:5, to investigate the reactivity of cellulose in lignocellulosic biomass. Thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FTIR) showed that the CE samples remained unaltered at temperatures up to 220 °C, but were significantly decomposed at 230 °C producing a thermal recalcitrant aromatic and high energy-dense material. FTIR showed that dehydration and aromatization reactions occurred at temperature equal or higher than 230 °C for the CE samples while a similar incre…

Thermogravimetric analysis020209 energyGeneral Chemical EngineeringEnergy Engineering and Power TechnologyLignocellulosic biomass02 engineering and technologyHydrothermal carbonizationBirchwoodchemistry.chemical_compoundHydrothermal carbonization020401 chemical engineeringSettore BIO/13 - Biologia Applicata0202 electrical engineering electronic engineering information engineeringSolid biofuelLignin0204 chemical engineeringCelluloseFourier transform infrared spectroscopyAromatizationAcid hydrolysiCellulose reactivityFuel TechnologychemistryAcid hydrolysisNuclear chemistrySettore AGR/16 - Microbiologia Agraria
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The effect of feedstock origin and temperature on the structure and reactivity of char from pyrolysis at 1300–2800 °C

2018

This study reports the effect of feedstock origin, residence time, and heat treatment temperature on CO2 and O2 reactivities, nanostructure and carbon chemistry of chars prepared at 1300, 1600, 2400, and 2800 °C in a slow pyrolysis reactor. The structure of char was characterized by transmission electron microscopy and Raman spectroscopy. The CO2 and O2 reactivity of char was investigated by thermogravimetric analysis. Results showed that the ash composition and residence time influence the char reactivity less than the heat treatment temperature. The heat treatment temperature and co-pyrolysis of pinewood char with biooil decreased the CO2 reactivity, approaching that of metallurgical coke…

Thermogravimetric analysisBiooilHigh-temperature pyrolysis020209 energyGeneral Chemical EngineeringEnergy Engineering and Power Technologychemistry.chemical_element02 engineering and technologyRaw materialsymbols.namesake020401 chemical engineeringMaschinenbau0202 electrical engineering electronic engineering information engineeringReactivity (chemistry)Char0204 chemical engineeringOrganic ChemistryReactivityMetallurgical cokeFuel TechnologychemistryChemical engineeringTransmission electron microscopyBiomass charsymbolsRaman spectroscopyCarbonPyrolysis
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Surface and bulk changes of a Pt 1%/Ce0.6Zr0.4O2 catalyst during CO oxidation in the absence of O2

2004

The reduction of a Pt 1%/Ce0.6Zr0.4O2 catalyst by CO in the absence of gaseous oxygen was studied by transient reactivity tests, temperature programmed surface reaction with CO, flow thermogravimetric tests and DRIFTS experiments, in order to obtain information generally on the OSC properties and, specifically, on the mechanism of CO oxidation over both, Pt catalyst and support-only sample (Ce0.6Zr0.4O2). The results of thermogravimetric experiments showed the presence of an induction time in the weight change % of the catalyst, depending on the CO concentration in the gas flow. This induction time could be related to the presence of two oxygen reactive sites. The first one leads to strongl…

Thermogravimetric analysisChemistryInorganic chemistryWeight changeAnalytical chemistrychemistry.chemical_elementInduction timeGeneral ChemistrySurface reactionOxygenCatalysisCatalysischemistry.chemical_compoundCarbonateReactivity (chemistry)
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Nanocrystalline ZnCO3—A novel sorbent for low-temperature removal of H2S

2013

Abstract The reactivity of a nanocrystalline ZnCO 3 toward H 2 S (0.2 vol% in N 2 /H 2 mixture) at 140–180 °C was characterized by thermal gravimetric analysis and by breakthrough curves measurements. We have found that under used conditions transformation of ZnCO 3 into ZnS is complete and the rate determining step of the sulfidation is the surface reaction. Such behavior is in strike contrast with that of ZnO whose sulfidation is severely limited by diffusion. The higher reactivity of ZnCO 3 in comparison with ZnO is attributed to the different microstructure of ZnS layer formed in these materials after a partial sulfidation. As in ZnO–ZnS transformation the molar volume increases (from 1…

Thermogravimetric analysisEnvironmental EngineeringMaterials scienceSorbentHealth Toxicology and MutagenesisInorganic chemistryCarbonatesTemperatureSulfidationOxideMicrostructureRate-determining stepPollutionNanocrystalline materialchemistry.chemical_compoundchemistryZinc CompoundsNanoparticlesEnvironmental ChemistryReactivity (chemistry)Hydrogen SulfideWaste Management and DisposalJournal of Hazardous Materials
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Upgrade of citrus waste as a biofuel via slow pyrolysis

2015

Abstract Slow pyrolysis (200–650 °C) experiments on citrus residues (orange peel waste “OP” and lemon peel waste “LP”) were carried out in lab scale fixed bed batch reactor. Bio-oil and bio-char obtained by thermal degradation are more stable, more homogeneous and higher energy content fuels when compared to the parent feedstock. Thermogravimetric analysis (TGA) showed higher stability of LP waste, which appears related to the higher lignin content . Mass and energy yields of solid and liquid products (i.e., char and oil) were measured to determine the effects of peak temperature on feedstock. A linear correlation between Gross Calorific Value (GCV), peak temperatures and mass loss (ML) all…

Thermogravimetric analysisFixed-bed reactorChemistryChemistry (all)Batch reactorAnalytical chemistrychemistry.chemical_elementPyrolysiRaw materialChar reactivityNitrogenAnalytical ChemistryEnergy densityFuel TechnologyBiofuelCitrus peel wasteSettore ING-IND/10 - Fisica Tecnica IndustrialeOrganic chemistryChemical Engineering (all)Heat of combustionCharPyrolysisJournal of Analytical and Applied Pyrolysis
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A tris-oxovanadium pyrogallate complex: synthesis, structure, and magnetic and electronic properties

2021

International audience; With the aim of identifying new cation-phenolate complexes, we herein investigated the reactivity of pyrogallol (H(3)pgal) with vanadium salts. A trimetallic anionic complex was identified, and found to be formed under a broad set of reaction conditions. This complex, with the formula V3O3(pgal)(3)(3-), consists of three oxovanadium(iv) units connected together by three pyrogallate ligands to afford a bowl-shaped species presenting a pseudo 3-fold symmetry axis. Its crystal structure is reported, as well as its characterisation by a broad set of techniques, including powder X-ray diffraction, thermogravimetric analysis, infrared and Raman spectroscopy, and solid stat…

Thermogravimetric analysisMaterials science010405 organic chemistryInfraredQuímica organometàl·licaVanadiumchemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryCompostos orgànics Síntesisymbols.namesakeCrystallographychemistry[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]symbolsMetal-organic frameworkReactivity (chemistry)Diffuse reflectionRaman spectroscopyDalton Transactions
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Characterization and reactivity of charcoal from high temperature pyrolysis (800-1600°C)

2019

This study presents the effect of wood origin and heat treatment temperature on the CO2 reactivity, nanostructure and carbon chemistry of chars prepared at 800, 1200, and 1600 °C in slow pyrolysis reactors. The structure of charcoal was characterized by transmission electron microscopy, Raman spectroscopy, mercury intrusion porosimetry and N2 adsorption. The CO2 reactivity of char was investigated by thermogravimetric analysis. Results showed that spruce and oak chars have similar reactivity at all heat treatment temperatures. The oak char prepared at 1600 °C contained long and flat graphene layers and interplanar distance that is similar to graphite and thus, was more ordered t…

Thermogravimetric analysisMaterials science020209 energyGeneral Chemical EngineeringChemieEnergy Engineering and Power Technologychemistry.chemical_element02 engineering and technologyAdsorption020401 chemical engineering0202 electrical engineering electronic engineering information engineeringReactivity (chemistry)CharGraphite0204 chemical engineeringCharcoallow heating rateOrganic Chemistrynon-graphitizing carbonCO2 reactivityFuel TechnologyChemical engineeringchemistryhigh-temperature pyrolysisvisual_artvisual_art.visual_art_mediumPyrolysisCarboncharcoal
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