Search results for "LEAN"

showing 10 items of 3611 documents

Reactivity of lithium β‑ketocarboxylates: the role of lithium salts

2017

Lithium beta-ketocarboxylates 1(COOLi), prepared by the reaction of lithium enolates 2(Li+) with carbon dioxide, readily decarboxylate in THF solution unless in the presence of lithium salts, in which case they are indefinitely stable at room temperature in inert atmosphere. The availability of stable THF solutions of lithium beta-ketocarboxylates 1(COOLi) in the absence of carbon dioxide allowed reactions to take place with nitrogen bases and alkyl halides 3 to give alpha-alkyl ketones 1(R) after acidic hydrolysis. The sequence thus represents the use of carbon dioxide as a removable directing group for the selective monoalkylation of lithium enolates 2(Li+). The roles of lithium salts in …

chemistry.chemical_classification010405 organic chemistryChemistryInorganic chemistryHalidechemistry.chemical_elementDisproportionationGeneral Chemistry010402 general chemistry01 natural sciences7. Clean energyBiochemistryNitrogenCatalysis0104 chemical sciencesHydrolysisColloid and Surface ChemistryPolymer chemistryReactivity (chemistry)LithiumInert gasQuímica orgànicaAlkyl
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Unveiling the high reactivity of benzyne in the formal [3+2] cycloaddition reactions towards thioamides through the Molecular Electron Density Theory

2020

Abstract The domino reaction of benzyne with thioamide has been studied within the Molecular Electron Density Theory (MEDT) at the MPWB1K/6-311G(d) level. This domino reaction takes place through i) a formal [3 + 2] cycloaddition (32CA) reaction affording an ammonium ylide, and ii) an extrusion of ethylene from this species yielding a dihydrothiazole. Topological analysis of the electron density of benzyne shows its pseudodiradical structure, that is, without any energy cost, changes to a carbenoid one, allowing its participation as electrophile in polar reactions. As a consequence, the formal 32CA reaction does not have an activation enthalpy. Analysis of the changes of electron density al…

chemistry.chemical_classification010405 organic chemistryOrganic Chemistry010402 general chemistry7. Clean energy01 natural sciencesBiochemistryCycloaddition0104 chemical sciencesElimination reactionCascade reactionchemistryYlideComputational chemistryIntramolecular forceDrug DiscoveryElectrophileReactivity (chemistry)CarbenoidTetrahedron
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Rapid Synthesis of Unsymmetrical Sulforhodamines Through Nucleophilic Amination of a Monobrominated Sulfoxanthene Dye

2014

A transition-metal-free method for the synthesis of N-substituted unsymmetrical sulforhodamine fluorophores from an unusual monobrominated sulfoxanthene dye and primary or secondary amines by direct SNAr-type reactions is presented. The simplicity and effectiveness of this “postamination” procedure were demonstrated through the rapid preparation of a library of multifunctional red-emitting rhodamine analogues. Some of these analogues are equipped with a reactive handle and retain the two water-solubilizing sulfonic acid moieties of the starting halogenated derivative; this makes them ideal candidates for biolabeling applications. The potential utility of this expeditious strategy to finely …

chemistry.chemical_classification010405 organic chemistryOrganic ChemistrySulfonic acid010402 general chemistryPhotochemistry01 natural sciences7. Clean energyFluorescence0104 chemical sciencesRhodaminechemistry.chemical_compoundchemistryCyclenNucleophileNucleophilic substitutionAmine gas treatingPhysical and Theoretical ChemistryAminationEuropean Journal of Organic Chemistry
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Triterpene saponins from Eryngium kotschyi

2015

Four new oleanane-type saponins 3-O-alpha-L-rhamnopyranosyl-(1 -> 4)-beta-D-glucuronopyranosyl-22-O-beta, beta-dimethylacryloylA1-barrigenol (1), 3-O-alpha-L-rhamnopyranosyl-(1 -> 4)-beta-D-glucuronopyranosyl-22-O-angeloylA1-barrigenol (2), 3-O-beta-D-glucopyranosyl-(1 -> 2)-[beta-D-glucopyranosyl-(1 -> 6)]-beta-D-glucopyranosyl-21,22,28-O-triacetyl-(3 beta,21 beta,22 alpha)-olean-12-en-16-one (3), and 3-O-beta-D-glucopyranosyl-(1 -> 2)-glucopyranosyl-22-O-beta-D-glucopyranosylsteganogenin (4), along with the known 3-O-beta-D-galactopyranosyl-(1 -> 2)-[alpha-L-arabinopyranosyl-(1 -> 3)]-beta-D-glucuronopyranosyl-22-O-angeloylA1-barrigenol and 3-O-alpha-L-rhamnopyranosyl-(1 -> 4)-beta-D-gluc…

chemistry.chemical_classificationApiaceaeKetoneMolecular StructureTurkeybiologyEryngiumStereochemistryStereoisomerismPlant ScienceGeneral MedicineSaponinsHorticulturebiology.organism_classificationPlant RootsBiochemistryEryngium kotschyichemistryTriterpeneOleanolic AcidNuclear Magnetic Resonance BiomolecularMolecular BiologyTwo-dimensional nuclear magnetic resonance spectroscopy
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The effect of iron on the biodegradation of natural dissolved organic matter

2016

Iron (Fe) may alter the biodegradation of dissolved organic matter (DOM), by interacting with (DOM), phosphorus (P) and microbes. We isolated DOM and a bacterial community from boreal lake water and examined bacterial growth on DOM in laboratory experiments. Fe was introduced either together with DOM (DOM-Fe) or into bacterial suspension, which led to the formation of insoluble Fe-precipitates on bacterial surfaces (Fe coating). In the latter case, the density of planktonic bacteria was an order of magnitude lower than that in the corresponding treatment without introduced Fe. The association of Fe with DOM decreased bacterial growth, respiration, and growth efficiency compared with DOM alo…

chemistry.chemical_classificationAtmospheric Science010504 meteorology & atmospheric sciencesEcologyPhosphorusPaleontologySoil ScienceBiomasschemistry.chemical_elementForestry010501 environmental sciencesAquatic ScienceBacterial growthBiodegradation01 natural sciences6. Clean waterBioavailabilitychemistryEnvironmental chemistryDissolved organic carbonRespirationOrganic matter0105 earth and related environmental sciencesWater Science and TechnologyJournal of Geophysical Research: Biogeosciences
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Persistent photovoltage in methylammonium lead iodide perovskite solar cells

2014

Open circuit voltage decay measurements are performed on methylammonium lead iodide (CH3NH3PbI3) perovskite solar cells to investigate the charge carrier recombination dynamics. The measurements are compared to the two reference polymer-fullerene bulk heterojunction solar cells based on P3HT:PC60BM and PTB7:PC70BM blends. In the perovskite devices, two very different time domains of the voltage decay are found, with a first drop on a short time scale that is similar to the organic solar cells. However, two major differences are also observed. 65-70% of the maximum photovoltage persists on much longer timescales, and the recombination dynamics are dependent on the illumination intensity.

chemistry.chemical_classificationCondensed Matter - Materials ScienceMaterials scienceOrganic solar cellOpen-circuit voltagelcsh:BiotechnologyDrop (liquid)IodideGeneral EngineeringMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciences7. Clean energylcsh:QC1-999Polymer solar cell3. Good healthchemistryChemical physicslcsh:TP248.13-248.65General Materials ScienceCharge carrierddc:621lcsh:PhysicsVoltagePerovskite (structure)APL Materials
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Polymer solar cells based on diphenylmethanofullerenes with reduced sidechain length

2011

Diphenylmethanofullerenes (DPMs) show interesting properties as acceptors in polymer bulk heterojunction solar cells due to the high open circuit voltages they generate compared to their energy levels. Here we investigate the effect of reducing the alkane sidechain length of the DPMs from C12 to C6 in the properties of the solar cell. This change leads to an increase in the electron mobility, thus allowing for a lower fullerene content, which in turn results in an increase in the short circuit current and, finally, in an increase in the efficiency of the device (from 2.3 to 2.6%) due to the higher concentration of the more absorbing polymer in the film. Atomic force microscopy images and ex…

chemistry.chemical_classificationElectron mobilityFullereneMaterials scienceOpen-circuit voltage02 engineering and technologyGeneral ChemistryPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences7. Clean energyPolymer solar cell0104 chemical scienceslaw.inventionchemistryChemical engineeringlawSolar cellMaterials ChemistryOrganic chemistryCrystallization0210 nano-technologyShort circuit
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New Triterpenoid and Ergostane Glycosides from the Leaves of Hydrocotyle umbellata L.

2011

Two new triterpenoid glycosides, together with two new ergostane glycosides, umbellatosides A–D (1–4, resp.), have been isolated from the leaves of Hydrocotyle umbellata L. Their structures were established by 2D-NMR spectroscopic techniques (1H,1H-COSY, TOCSY, NOESY, HSQC, and HMBC) and mass spectrometry as 3β,22β-dihydroxy-3-O-[α-L-rhamnopyranosyl-(12)-β-D-glucuronopyranosyl]olean-12-en-28-oic acid 28-O-β-D-glucopyranosyl ester (1), 3-O-[α-L-rhamnopyranosyl-(12)-β-D-glucuronopyranosyl]oleanolic acid 28-O-β-D-glucopyranosyl ester (2), (3β,11α,26)-ergosta-5,24(28)-diene-3,11,26-triol 3-O-(β-D-glucopyranosyl)-11-O-(α-L-rhamnopyranosyl)-26-O-β-D-glucopyranoside (3), and (3β,11α,21,26)-ergosta…

chemistry.chemical_classificationErgostanebiologyStereochemistryOrganic ChemistryGlycosideHydrocotyle umbellataMass spectrometrybiology.organism_classificationBiochemistryCatalysisInorganic ChemistryTerpenechemistry.chemical_compoundTriterpenoidchemistryDrug DiscoveryOrganic chemistryPhysical and Theoretical ChemistryOleanolic acidTwo-dimensional nuclear magnetic resonance spectroscopyHelvetica Chimica Acta
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A new oleanane glycoside from the roots ofAstragalus caprinus

2006

A novel oleanane-type triterpene saponin (1) together with two known molecules, soyasapogenol B and astragaloside VIII were isolated from the roots of Astragalus caprinus. Their structural elucidation was performed mainly by 2D NMR techniques (COSY, TOCSY, NOESY, HSQC, HMBC) and mass spectrometry. Compound 1 was determined as 3-O-[alpha-L-rhamnopyranosyl-(1 --> 2)-beta-D-glucuronopyranosyl]-22-O-beta-D-apiofuranosyl-soyasapogenol B.

chemistry.chemical_classificationMagnetic Resonance SpectroscopyMolecular StructureChemistryStereochemistrySaponinGlycosideAstragalus PlantGeneral ChemistryNuclear magnetic resonance spectroscopyPlant Rootschemistry.chemical_compoundAstragalosideTriterpeneOrganic chemistryGeneral Materials ScienceGlycosidesOleanolic AcidOleananeTwo-dimensional nuclear magnetic resonance spectroscopyHeteronuclear single quantum coherence spectroscopyMagnetic Resonance in Chemistry
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Fast and continuous synthesis of nanostructured iron spinel in supercritical water: influence of cations and citrates

2014

International audience; Spinel iron oxide nanoparticles were obtained under supercritical water conditions in a continuous and fast (less than 10s) way by modifying the initial stoichiometric Fe II /Fe III molar ratio from (1/2) to (3/0), without base solution, and using citrates directly with iron precursors. This result opens the way of an economical and environmentally benign approach to synthesize superparamagnetic iron oxide nanoparticles (SPIONs) in important yields.

chemistry.chemical_classificationMaterials scienceBase (chemistry)Superparamagnetic iron oxide nanoparticlesGeneral Chemical EngineeringSpinelInorganic chemistry02 engineering and technologyGeneral Chemistryengineering.material010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences7. Clean energySupercritical fluid0104 chemical scienceschemistry.chemical_compoundchemistryMolar ratioengineeringIron oxide cycle[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics0210 nano-technologyStoichiometryIron oxide nanoparticles
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