Search results for "reactions"

showing 10 items of 631 documents

Stopped-Flow and DFT Studies of Proton Transfer and Isomerization of 5-Amino-3-imino-1,2,6,7-tetracyano-3H-pyrrolizine and Its Related Base 2-(5-Amin…

2001

International audience; A complete kinetic study of pH-dependent isomerization of 5-amino-3-imino-1,2,6,7-tetracyano-3H-pyrrolizine (HL) and 2-(5-amino-3,4-dicyano-2H-pyrrol-2-ylidene)-1,1,2-tricyanoethanide (L‘-) in the pH range from −0.5 to +13 in aqueous solution, which spans over 7 orders of magnitude for the pseudo-first-order rates (log k from −4.8 to +2.5), has revealed for the first time the existence of the corresponding conjugate species L- and HL‘. The study has allowed the determination of the acid dissociation constants of HL (pKa) and HL‘ (pKa‘), as well as all of the individual forward and reverse isomerization rates of the acidic (HL/HL‘) and basic (L-/L‘-) forms. Although L…

chemistry.chemical_classificationIsomerizationAqueous solutionBase (chemistry)ProtonStereochemistryEquilibrium[CHIM.ORGA]Chemical Sciences/Organic chemistryProtonation02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesDecompositionAcid dissociation constant0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryKineticschemistryOrganic reactionsKinetic parametersPhysical and Theoretical Chemistry0210 nano-technologyIsomerizationConjugate
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Synthesis of brominated tetrathiafulvalenes via phosphite-mediated cross-coupling

2010

The synthesis of polybrominated tetrathiafulvalenes (TTF-Brn, 2-4) containing 2-4 bromine atoms via phosphite-mediated cross-coupling of bromo-substituted 1,3-dithiole-2-thiones and 1,3-dithiole-2-ones is reported. © 2010 Elsevier B.V.

chemistry.chemical_classificationKetoneBromineHalogenationLithiationChemistryMechanical EngineeringMetals and AlloysCross reactionschemistry.chemical_elementHalogenationCondensed Matter PhysicsChemical synthesisElectronic Optical and Magnetic MaterialsCoupling (electronics)Brominated tetrathiafulvalenesPhosphite cross-couplingMechanics of MaterialsPolymer chemistryMaterials ChemistryOrganic chemistrySynthetic Metals
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Carbon nitride as photocatalyst in organic selective transformations

2020

Abstract Graphitic carbon nitride (g-C3N4) is a metal-free conjugated polymer which has become a new research hotspot in photocatalysis. It can be used for solar energy exploitation like in solar energy organic synthesis, one of the most new and appealing green applications of heterogeneous photocatalysis. This chapter resumes the state-of-the-art and progresses in the application of heterogeneous visible light photocatalysis in organic selective transformations by using C3N4 as photocatalyst.

chemistry.chemical_classificationMaterials sciencebusiness.industryGraphitic carbon nitrideNanotechnologyPolymerConjugated systemSolar energychemistry.chemical_compoundchemistryC-C formation Carbon nitride Coupling reactions Organic synthesis Organic transformations Partial oxidationPhotocatalysisOrganic synthesisSettore CHIM/07 - Fondamenti Chimici Delle TecnologiebusinessCarbon nitrideVisible spectrum
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A new strategy for the synthesis of fluorinated 3,4-dihydropyrimidinones

2009

A new family of 3,4-dihydropyrimidinones (DHPMs) bearing fluorinated substituents at C6 have been prepared from gem-difluorinated nitriles, alkyl 3-butenoates and iso(thio)cyanates. This novel Biginelli-type process relies on the gamma-addition of the ester-derived enolate to fluorinated nitriles. A tandem nucleophilic addition aza-Michael reaction sequence completes the synthetic process. (C) 2009 Elsevier B.V. All rights reserved.

chemistry.chemical_classificationNucleophilic additionFluorinated nitrilesTandemChemistryOrganic ChemistryThio-BiochemistryInorganic ChemistryReaction sequenceMulticomponent reactionsEnvironmental ChemistryOrganic chemistryFluorinated dihydropyrimidinonesPhysical and Theoretical ChemistryAlkylIntramolecular aza-Michael reaction
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Overview on oxidation mechanisms of organic compounds by TiO2 in heterogeneous photocatalysis

2012

This review provides the reader with a general overview on heterogeneous photocatalytic oxidation mechanisms in the presence of TiO2, with a special address to conversion of aliphatic and aromatic organic species. The aim was to clarify the steps of the photo-oxidation of the various classes of compounds and to relate them with the properties of the catalysts and the experimental conditions used. Reactions carried out to perform complete degradation and photocatalytic partial oxidations have been deeply discussed. Recent isotopic studies highlighted new reaction pathways concerning partial oxidation of alcohols to aldehyde and oxidation of benzene while EPR investigations confirmed that not…

chemistry.chemical_classificationReaction mechanismRadicalOrganic ChemistryPhotochemistryAldehydeCatalysisCatalysischemistry.chemical_compoundchemistryOrganic reactionPhotocatalysisPartial oxidationSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical ChemistryPhotocatalysis Reaction mechanisms Organic reactions TiO2Benzene
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A Headful of T4 Coliphage DNA Packaged to Fasces-Like Globules in Fractal Models

1998

We present a new model for T4 DNA packaging based on fractal considerations. The proposed model is based on electron microscopic observations of spread and packaged DNA. The model takes into account enzymatically and unidirectionally driven packaging, and quick release of the DNA during infection. We also consider the different biochemical reactions of the packaging process.

chemistry.chemical_compoundFractalMaterials sciencechemistrybiologyBiophysicsActive packagingBiochemical reactionsColiphagebiology.organism_classificationElectron microscopicDna packagingDNA
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1,2,4-Oxadiazole rearrangements involving an NNC side-chain sequence.

2009

The thermal rearrangement of N-1,2,4-oxadiazol-3-yl-hydrazones into 1,2,4-triazole derivatives is reported. This represents the first example of a three-atom side-chain rearrangement involving an NNC sequence linked at the C(3) of the oxadiazole. The reactions carried out under solvent-free conditions produced good to high yields of the final products.

chemistry.chemical_compoundchemistryStereochemistryOrganic ChemistrySide chainTriazoleoxadiazole triazole solvent-free reactions heterocyclic rearrangementOxadiazoleSettore CHIM/06 - Chimica OrganicaPhysical and Theoretical ChemistryBiochemistrySequence (medicine)Organic letters
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Palladium-based catalytic systems for the synthesis of conjugated enynes by Sonogashira reactions and related alkynylations

2007

Conjugated alkynes are recurring building blocks in natural products, a wide range of industrial intermediates, pharmaceuticals and agrochemicals, and molecular materials for optics and electronics. The palladium-catalyzed cross-coupling between sp(2)-hybridized carbon atoms of aryl, heteroaryl, and vinyl halides with sp-hybridized carbon atoms of terminal acetylenes is one of the most important developments in the field of alkyne chemistry over the past 50 years. The seminal work of the 1970s has initiated an intense search for more general and reliable reaction conditions. The interest in the catalytic activation of demanding substrates, the need to minimize the consumption of depletive r…

chemistry.chemical_elementSonogashira couplingAlkyneHalideConjugated systemHeterogeneous catalysis010402 general chemistryalkynes01 natural sciencesCatalysisCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/CatalysisOrganometallic Compoundscross-couplingOrganic chemistryComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationMolecular Structure010405 organic chemistryArylStereoisomerismGeneral ChemistryGeneral Medicine[CHIM.CATA]Chemical Sciences/Catalysissonogashira reactionspalladiumCombinatorial chemistry0104 chemical sciencesheterogeneous catalysischemistryCarbonPalladium
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Organocatalytic Domino Oxa-Michael/1,6-Addition Reactions: Asymmetric Synthesis of Chromans Bearing Oxindole Scaffolds.

2016

An asymmetric organocatalytic domino oxa-Michael/1,6-addition reaction of ortho-hydroxyphenyl-substituted para-quinone methides and isatin-derived enoates has been developed. In the presence of 5 mol % of a bifunctional thiourea organocatalyst, this scalable domino reaction affords 4-phenyl-substituted chromans bearing spiro-connected oxindole scaffolds and three adjacent stereogenic centers in good to excellent yields (up to 98 %) and with very high stereoselectivities (up to >20:1 d.r., >99 % ee).

chromansAddition reaction010405 organic chemistrydomino reactionspara-quinone methidesEnantioselective synthesisGeneral MedicineGeneral Chemistry010402 general chemistry01 natural sciencesoxa-Michael additionCatalysisDomino0104 chemical sciencesStereocenterchemistry.chemical_compoundchemistryCascade reactionOrganocatalysisOrganic chemistryorganocatalysisOxindoleBifunctionalta116Angewandte Chemie (International ed. in English)
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Neutron halos in the excited states of 12B

2018

The differential cross sections of the 11B(d,p) 12B reaction leading to formation of the 1+ ground state and the 0.95-MeV 2+, 1.67-MeV 2−, 2.62-MeV 1−, 2.72-MeV 0+, and 3.39-MeV 3− excited states of 12B are measured at Ed = 21.5 MeV. The analysis of the data is carried out within the coupled-reaction-channels method for the direct neutron transfer and the Hauser-Feshbach formalism of the statistical compound-nucleus model. The spectroscopic factors, asymptotic normalization coefficients, and rms radii of the last neutron in all states studied are deduced. The existence of the neutron halos in the 1.67-MeV 2− and 2.62-MeV 1− states is found, consistent with the earlier published data. New in…

cluster modelselectromagnetic momentsNuclear Theorynucleon distributiontransfer reactionsbooriPhysics::Accelerator Physicsspectroscopic factorsdirect reactionsNuclear Experimentydinfysiikka
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