Search results for "Bases"

showing 10 items of 1240 documents

Switching and redox isomerism in first-row transition metal complexes containing redox active Schiff base ligands.

2014

International audience; The reversible redox isomerisms in first row transition metal complexes of the type ML2 were studied. The six ML2 complexes (M = Mn(III) (), Fe(II) (), Co(III) (), Ni(II) (), Cu(II) () and Zn(II) ()) were synthesized with a redox active Schiff base ligand [2-(3,5-di-tert-butyl-2-hydroxyphenylamino)-4-chlorophenol] (H3L) presenting different oxidation states from -2 to 0 (L(2-), L(-) and L(0)). EPR spectra and magnetic susceptibility measurements indicate the presence of complexes of the type [Mn(III)(L(2-))(L(-))] () with S = 1/2, [Fe(II)(L(-))2] () with S = 2, [Co(III)(L(2-))(L(-))] () with S = 1/2, [Ni(II)(L(-))2] () with S = 1, [Cu(II)(L(-))2] () with S = 1/2 and …

010402 general chemistryLigands01 natural sciencesRedoxlaw.inventionInorganic Chemistrychemistry.chemical_compoundElectron transferTransition metalIsomerismlawCoordination ComplexesMetals HeavyElectron paramagnetic resonanceSchiff BasesValence (chemistry)Schiff base010405 organic chemistryLigand[CHIM.MATE]Chemical Sciences/Material chemistryTautomer0104 chemical sciences3. Good healthCrystallographychemistryOxidation-Reduction
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9,10-Phenanthrenedione as Visible-Light Photoredox Catalyst: A Green Methodology for the Functionalization of 3,4-Dihydro-1,4-Benzoxazin-2- Ones thro…

2018

A visible-light photoredox functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones through a Friedel-Crafts reaction with indoles using an inexpensive organophotoredox catalyst is described. The reaction uses a dual catalytic system that is formed by a photocatalyst simple and cheap, 9,10-phenanthrenedione, and a Lewis acid, Zn(OTf)2. 5W white LEDs are used as visible-light source and oxygen from air as a terminal oxidant, obtaining the corresponding products with good yields. The reaction can be extended to other electron-rich arenes. Our methodology represents one of the most valuable and sustainable approach for the functionalization of 3,4-dihydro-1,4-benzoxazin-2-ones, as compared to th…

010402 general chemistrylcsh:Chemical technology01 natural sciencesCatalysisCatalysislcsh:Chemistrychemistry.chemical_compoundCatàlisiTryptophollcsh:TP1-1185Lewis acids and basesorganic_chemistryPhysical and Theoretical ChemistryFriedel-Crafts reactionFriedel–Crafts reaction010405 organic chemistryindolesCombinatorial chemistry0104 chemical scienceschemistrylcsh:QD1-999visible-light photocatalysis14-benzoxazin-2-onesPhotocatalysisSurface modificationorganophotoredox catalysisQuímica orgànicaDerivative (chemistry)Visible spectrum
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Dual role of silver in a fluorogenic N-squaraine probe based on Ag(i)–π interactions

2021

In the presence of Ag(I), the monoanion of cyano-N-squaraine (I) generates an intense fluorescence turn-on response. Experimental evidence and DFT calculations reveal a sequence of deprotonation-coordination events in which the Ag(I) ions play a dual role as a Lewis acid and coordinating metal. The observed effect is highly selective for Ag(I) compared to other metals.

010405 organic chemistryChemistry010402 general chemistryHighly selective01 natural sciences0104 chemical sciencesIonInorganic ChemistryMetalCrystallographyDual rolevisual_artIntense fluorescencevisual_art.visual_art_mediumLewis acids and basesSequence (medicine)Dalton Transactions
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Lewis Base Catalyzed Intramolecular Reduction of Salicylaldehydes by Pinacol-Derived Chlorohydrosilane

2018

010405 organic chemistryHydrosilylationPinacolOrganic ChemistryHomogeneous catalysis010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisReduction (complexity)chemistry.chemical_compoundchemistryIntramolecular forceLewis acids and basesPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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A robust viologen and Mn-based porous coordination polymer with two types of Lewis acid sites providing high affinity for H 2 O, CO 2 and NH 3

2017

A novel porous coordination polymer [Mn(pc3)(H2O)2]·xH2O (3 < x < 4) is synthesized in water at pH = 7 using the anionic viologen-carboxylate ligand 4,4′-bipyridinium,1,1′-bis-(2,4-dicarboxyphenyl) (pc32−). Dehydration of the material results in the formation of open pores containing two types of accessible Lewis acid sites: exposed Mn2+ cations and N+ atoms of viologen units. Due to this property the PCP shows high affinity and capacity in the adsorption of H2O, CO2 and NH3. Despite the presence of strong adsorption sites this material is stable in liquid water and in gaseous NH3.

010405 organic chemistryLiquid waterCoordination polymerLigandInorganic chemistryViologen010402 general chemistrymedicine.disease01 natural sciences0104 chemical sciencesInorganic Chemistry[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundAdsorptionchemistrymedicine[CHIM]Chemical SciencesLewis acids and basesDehydrationPorosityComputingMilieux_MISCELLANEOUSmedicine.drug
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Enantioselective synthesis of chiral oxazolines from unactivated ketones and isocyanoacetate esters by synergistic silver/organocatalysis

2018

[EN] A multicatalytic approach that combines a bifunctional Brønsted base¿squaramide organocatalyst and Ag+ as Lewis acid has been applied in the reaction of unactivated ketones with tert-butyl isocyanoacetate to give chiral oxazolines bearing a quaternary stereocenter. The formal [3+2] cycloaddition provided high yields of the corresponding cis-oxazolines with good diastereoselectivity and excellent enantioselectivity, being applied to aryl¿alkyl and alkyl¿alkyl ketones.

010405 organic chemistryMetals and AlloysEnantioselective synthesisGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisCycloaddition0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStereocenterchemistry.chemical_compoundchemistryCatàlisiFISICA APLICADAOrganocatalysisMaterials ChemistryCeramics and CompositesLewis acids and basesBifunctionalQuímica orgànica
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Comparative hydroamination of aniline and substituted anilines with styrene on different zeolites, triflate based catalysts and their physical mixtur…

2014

Abstract Catalytic performances of different zeolites (Beta and mordenites), scandium triflate based catalysts, mesoporous UVM-7 encapsulated scandium triflate and physical mixtures prepared under ultrasound irradiation were evaluated in the hydroamination of aniline and substituted anilines with styrene. The performances of these catalysts were controlled by the type of acidity and strength. Thus, the conversion was mainly controlled by the strength of the acid sites and their accessibility, while the selectivity appeared to be controlled by the Lewis/Bronsted type of acidity. Lewis acid catalysts directed the reactions mainly to the formation of the Markovnikov adducts while Bronsted acid…

010405 organic chemistryProcess Chemistry and TechnologyMarkovnikov's rulechemistry.chemical_element010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundAnilinechemistryOrganic chemistryScandiumHydroaminationLewis acids and basesBrønsted–Lowry acid–base theoryTrifluoromethanesulfonateApplied Catalysis A: General
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A Ferrocenyl Amino Substituted Stannylene as an Intramolecular Fe→Sn Lewis Adduct

2018

010405 organic chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesAdductInorganic Chemistrychemistry.chemical_compoundchemistryFerroceneIntramolecular forceLewis acids and basesTinZeitschrift für anorganische und allgemeine Chemie
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Analysis of psychoactive substances in water by information dependent acquisition on a hybrid quadrupole time-of-flight mass spectrometer.

2016

Emerging drugs of abuse, belonging to many different chemical classes, are attracting users with promises of “legal” highs and easy access via internet. Prevalence of their consumption and abuse through wastewater-based epidemiology can only be realized if a suitable analytical screening procedure exists to detect and quantify them in water. Solid-phase extraction and ultra-high performance liquid chromatography quadrupole time-of-flight-mass spectrometry (UHPLC–QqTOF–MS/MS) was applied for rapid suspect screening as well as for the quantitative determination of 42 illicit drugs and metabolites in water. Using this platform, we were able to identify amphetamines, tryptamines, piperazines, p…

010501 environmental sciencesWastewaterMass spectrometryTandem mass spectrometry01 natural sciencesBiochemistryRiver waterHigh resolution mass spectrometryAnalytical ChemistryRiversTandem Mass SpectrometryQuantificationPsychoactive drugsHumansSample preparationSolid phase extractionQuadrupole time of flightChromatography High Pressure Liquid0105 earth and related environmental sciencesPsychotropic DrugsChromatographyChemistryIllicit Drugs010401 analytical chemistryOrganic ChemistrySolid Phase ExtractionWaterGeneral MedicineQuantitative determination0104 chemical sciencesWastewaterEnvironmental chemistryScreeningDatabases ChemicalWater Pollutants ChemicalJournal of chromatography. A
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Ecological genomics of adaptation to unpredictability in experimental rotifer populations

2019

AbstractElucidating the genetic basis of phenotypic variation in response to different environments is key to understanding how populations evolve. Facultatively sexual rotifers can develop adaptive responses to fluctuating environments. In a previous evolution experiment, diapause-related traits changed rapidly in response to two selective regimes (predictable vs unpredictable) in laboratory populations of the rotifer Brachionus plicatilis. Here, we investigate the genomic basis of adaptation to environmental unpredictability in these experimental populations. We identified and genotyped genome-wide polymorphisms in 169 clones from both selective regimes after seven cycles of selection usi…

0106 biological sciences0301 basic medicineAcclimatizationRotiferalcsh:MedicineGenomicsSingle-nucleotide polymorphismEvolutionary ecologyPolymorphism Single Nucleotide010603 evolutionary biology01 natural sciencesArticle03 medical and health sciencesAnimalsSelection Geneticlcsh:ScienceGenetic Association StudiesSelection (genetic algorithm)GenomeMultidisciplinarybiologylcsh:REcological geneticsBrachionusEcological geneticsbiology.organism_classificationPhenotype030104 developmental biologyEvolutionary biologylcsh:QEvolutionary ecologyAdaptationDatabases Nucleic AcidScientific Reports
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