Search results for "Reaction"

showing 10 items of 6134 documents

The first catalytic method for Heck alkynylation of unactivated aryl bromides (copper-free Sonogashira) in an ionic liquid: 1 mol-percent palladium/t…

2007

Herein we report the studies of Heck alkynylation (copper-free Sonogashira) with aryl halides (I, Br, Cl) employing various metallic precursors, tertiary phosphanes and bases in [BMIM][BF4] as the solvent. As a result, we provide the first method that allows the coupling of a large array of substrates, either activated or deactivated bromides in an ionic liquid. Furthermore, the system of highest efficiency is unexpectedly the simplest and cheaper combination that employs [Pd(η3-C3H5)Cl]2/PPh3 at only a 1 mol-% loading with pyrrolidine as the base and in the absence of a copper salt. The coupling of sterically and electronically deactivated bromides bearing different functional groups to ar…

copper-free SonogashiraIonic bondingchemistry.chemical_elementSonogashira coupling010402 general chemistry01 natural sciences7. Clean energyHeck alkynylationPyrrolidineCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/CatalysisHeck reactiontriphenylphosphaneOrganic chemistryPhysical and Theoretical ChemistryAlkylComputingMilieux_MISCELLANEOUSionic liquidchemistry.chemical_classificationcatalysis010405 organic chemistryArylOrganic ChemistryGeneral Medicine[CHIM.CATA]Chemical Sciences/CatalysispalladiumCombinatorial chemistrymethylimidazolium0104 chemical sciencesSolventchemistryIonic liquidPalladium
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An Overview on the Performance of 1,2,3-Triazole Derivatives as Corrosion Inhibitors for Metal Surfaces

2021

This review accounts for the most recent and significant research results from the literature on the design and synthesis of 1,2,3-triazole compounds and their usefulness as molecular well-defined corrosion inhibitors for steels, copper, iron, aluminum, and their alloys in several aggressive media. Of particular interest are the 1,4-disubstituted 1,2,3-triazole derivatives prepared in a regioselective manner under copper-catalyzed azide-alkyne cycloaddition (CuAAC) click reactions. They are easily and straightforwardly prepared compounds, non-toxic, environmentally friendly, and stable products to the hydrolysis under acidic conditions. Moreover, they have shown a good efficiency as corrosi…

corrosion inhibitorAzidesmetalQH301-705.5Surface PropertiesReviewCatalysisInorganic ChemistryPhysical and Theoretical ChemistryBiology (General)metal alloysMolecular BiologyQD1-999Spectroscopymechanism of inhibitionCycloaddition ReactionMolecular StructureOrganic ChemistryGeneral MedicineQuímicaTriazolesComputer Science ApplicationsCorrosionChemistryMetalsclick chemistry123-triazoleInternational Journal of Molecular Sciences
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Multiple solutions for semilinear Robin problems with superlinear reaction and no symmetries

2021

We study a semilinear Robin problem driven by the Laplacian with a parametric superlinear reaction. Using variational tools from the critical point theory with truncation and comparison techniques, critical groups and flow invariance arguments, we show the existence of seven nontrivial smooth solutions, all with sign information and ordered.

critical groupSettore MAT/05 - Analisi Matematicacritical point theoryConstant sign and nodal solutionsuperlinear reactionflow invariance
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Cross-coupling reactions of organoborons with organic halides

2011

cross-coupling reactionsorgaaninen kemiaboorisynthesis of arylbenzothiazole derivativesboronic derivativesreaktiotorganic halides
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Naphthalene-2,6-diyl bis(4-methylbenzenesulfonate)

2018

The complete molecule of the title compound, C24H20O6S2, is generated by a crystallographic inversion centre at the middle of the naphthalene ring system. The dihedral angle between the naphthalene ring system and the pendant benzene ring is 10.23 (6)° and the C—S—O—C torsion angle is −172.05 (10)°. In the crystal, weak C—H...O interactions link the molecules into (10-1) sheets.

crystal structure010405 organic chemistryChemistryGeneral MedicineCrystal structureDihedral angle010402 general chemistryRing (chemistry)01 natural sciencesCoupling reactioncrosscoupling reactions0104 chemical sciencesCrystalCrystallographychemistry.chemical_compoundSulfonatecross-coupling reactionslcsh:QD901-999lcsh:CrystallographyPhysics::Chemical PhysicsBenzenetosylatesNaphthaleneIUCrData
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4-Chloronaphthalen-1-yl 4-methylbenzenesulfonate

2018

In the title compound, C17H13ClO3S, the naphthalene ring system and the benzene ring of the tosylate substituent are inclined to one another by 55.32 (5)°. The crystal structure features weak intermolecular C—H...O hydrogen bonds, one of which forms inversion dimers. Additional C—H...O hydrogen bonds and weak Cl...Cl halogen bonds stack the molecules along the b-axis direction.

crystal structure010405 organic chemistryChemistryHydrogen bondSubstituentGeneral MedicineCrystal structure010402 general chemistryRing (chemistry)01 natural sciencesMedicinal chemistryCoupling reactioncrosscoupling reactions0104 chemical scienceschemistry.chemical_compoundSulfonatecross-coupling reactionsHalogenlcsh:QD901-999lcsh:CrystallographyPhysics::Chemical PhysicsBenzenetosylatesIUCrData
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3,5-Dimethoxyphenyl 4-methylbenzenesulfonate

2017

Molecules of the title compound, C15H16O5S, are composed of a 3,5-dimethoxyphenyl moiety substituted with a toluene-4-sulfonate group. The dihedral angle between two aromatic rings is 57.23 (4)°. In the crystal, molecules are connected by weak C—H...O hydrogen bonds and S...O van der Waals interactions.

crystal structure010405 organic chemistryHydrogen bondStereochemistryChemistryAromaticityCrystal structuretosyl­atesDihedral angle010403 inorganic & nuclear chemistry01 natural sciencesMedicinal chemistryCoupling reaction0104 chemical sciencessymbols.namesakechemistry.chemical_compoundSulfonatecross-coupling reactionssymbolsMoietyvan der Waals forceIUCrData
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3,5-Bis(trifluoromethyl)phenyl 4-methylbenzenesulfonate

2017

Molecules of the title compound, C15H10F6O3S, are composed of 3,5-bis(trifluoromethyl)phenyl substituted with a toluene-4-sulfonate group. The dihedral angle between two aromatic moieties is 45.10 (5)°. In the crystal, molecules are connected by weak C—H...O and C—H...F contacts. One of the trifluoromethyl groups is disordered.

crystal structure010405 organic chemistryMeth-Crystal structuretosyl­atesDihedral angle010402 general chemistry01 natural sciencesCoupling reaction0104 chemical sciencesCrystalchemistry.chemical_compoundSulfonatecross-coupling reactionschemistryGroup (periodic table)Polymer chemistryMethyl benzeneIUCrData
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Chlorido(2,2′-{[2-(1-methyl-1H-imidazol-2-yl-κN 3)imidazolidine-1,3-diyl-κN]bis(methylene)}bis(1-methyl-1H-imidazole-κN 3))copper(II) perchlorate

2019

In the crystal structure of the title complex, [CuCl(C17H24N8)]ClO4, the copper(II) metal exhibits an N4Cl pentacoordinate environment in a distorted square-pyramidal geometry. Coordination to the metal centre occurs through the three 1-methylimidazole N atoms from the pendant groups, one amine N atom from the imidazolidine moiety and one chlorido anion. Intermolecular interactions take place at two of the 1-methyl-imidazole rings in the form of parallel-displaced π–π stacking interactions forming chains parallel to the a axis. Three O atoms of the perchlorate anion are rotationally disordered between two orientations with occupancies of 0.5.

crystal structureCrystallographyCopper(II) perchlorate010405 organic chemistrychemistry.chemical_elementGeneral ChemistryCrystal structure010402 general chemistryCondensed Matter Physics01 natural sciencesMedicinal chemistryCopper0104 chemical sciencesPerchloratechemistry.chemical_compoundchemistryQD901-999ImidazolidineImidazoleMoietyGeneral Materials Scienceimidazolidine ligandEne reactioncopper complexActa Crystallographica Section E Crystallographic Communications
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Crystal structure and Hirshfeld surface analysis of 3-octyl-4-oxo-2,6-bis(3,4,5-trimethoxyphenyl)piperidinium chloride

2018

The title compound was synthesized by a one-pot Mannich condensation reaction. In the crystal, centrosymmetric dimers are linked into layers parallel to (011) by N—H⋯Cl and C—H⋯Cl hydrogen bonds. A Hirshfeld surface analysis indicates that O—H (20.5%) inter­actions make the largest contribution to the crystal packing.

crystal structureCyclohexane conformationCrystal structure010403 inorganic & nuclear chemistryRing (chemistry)01 natural sciencesMedicinal chemistryChlorideResearch CommunicationsCrystalchemistry.chemical_compoundMannich reactionmedicineHirshfeld surface analysisGeneral Materials ScienceBenzeneMannich reactionCrystallography010405 organic chemistryHydrogen bondChemistryGeneral ChemistryCondensed Matter Physics0104 chemical sciencesQD901-999piperidine-4-onemedicine.drugActa Crystallographica Section E Crystallographic Communications
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