Search results for "trifluoromethanesulfonate"

showing 10 items of 276 documents

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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Structural and metallo selectivity in the assembly of [2 × 2] grid-type metallosupramolecular species: Mechanisms and kinetic control

2011

An unsymmetrical bis(tridentate) ligand LH in which one binding site can be readily deprotonated forms a kinetically inert [Co(III)L(2)](+) complex which can be used as a "corner" species for the "Coupe du Roi" assembly of trans,trans-[Co(2)M(2)L(4)](6+) metallogrids (M = Fe(II), Co(II), Cu(II), Zn(II)). In the mixed Co(III)/Co(II) species, the oxidation states appear to be localised. In solution, the ligand LH forms octacationic, homometallic [2 × 2] grids with the individual labile metal ions Fe(II), Co(II), Cu(II), Zn(II), seemingly as mixtures of all possible isomers arising from the unsymmetrical nature of the ligand. In the solid state, however, [Zn(4)L(4)](CF(3)SO(3))(8)·4CH(3)CN cry…

010405 organic chemistryStereochemistryChemistryLigandMetal ions in aqueous solutionCrystal structure010402 general chemistry01 natural sciencesKinetic control0104 chemical sciencesInorganic ChemistryCrystallographyDeprotonation[CHIM]Chemical SciencesStereoselectivitySelectivityta116TrifluoromethanesulfonateComputingMilieux_MISCELLANEOUS
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CCDC 2182459: Experimental Crystal Structure Determination

2022

Related Article: Anni I. Taponen, Awatef Ayadi, Noora Svahn, Manu K. Lahtinen, Mathieu Rouzières, Rodolphe Clérac, Heikki M. Tuononen, Aaron Mailman|2022|Cryst.Growth Des.|22|7110|doi:10.1021/acs.cgd.2c00795

4-(1-n-butylpyridinium-3-yl)-1235-dithiadiazolyl radical trifluoromethanesulfonateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1401638: Experimental Crystal Structure Determination

2015

Related Article: Fangfang Pan, N. Kodiah Beyeh, Kari Rissanen|2015|RSC Advances|5|57912|doi:10.1039/C5RA11905G

5111723-tetrakis((cyclohexylammonio)methyl)-281420-tetramethyl-46101216182224-octahydroxycalix(4)arene tetrakis(trifluoromethanesulfonate) 14-dioxane solvate dihydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1522088: Experimental Crystal Structure Determination

2017

Related Article: Mikk Kaasik, Sandra Kaabel, Kadri Kriis, Ivar Järving, Riina Aav, Kari Rissanen, Tönis Kanger|2017|Chem.-Eur.J.|23|7337|doi:10.1002/chem.201700618

9-(4-(35-bis(trifluoromethyl)phenyl)-5-iodo-3-methyl-1H-123-triazol-3-ium-1-yl)-6'-methoxy-11'-dimethylcinchonan-11'-diium tris(trifluoromethanesulfonate) methanol solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Anion-Exchange Properties of Trifluoroacetate and Triflate Salts of N-Alkylammonium Resorcinarenes

2016

The synthesis of N-benzyl- and N-cyclohexylammonium resorcinarene trifluoroacetate (TFA) and triflate (OTf) salt receptors was investigated. Solid-state analysis by single-crystal X-ray diffraction revealed that the N-alkylammonium resorcinarene salts (NARSs) with different upper substituents had different cavity sizes and different affinities for anions. Anion-exchange experiments by mixing equimolar amounts of N-benzylammonium resorcinarene trifluoroacetate and N-cyclohexylammonium resorcinarene triflate, as well as N-benzylammonium resorcinarene triflate and N-cyclohexylammonium resorcinarene trifluoroacetate showed that the NARS with flexible benzyl groups preferred the larger OTf anion…

AnionsModels MolecularsaltsPhenylalanineElectrospray ionizationInorganic chemistrySalt (chemistry)Benzylammonium CompoundsCrystallography X-Ray010402 general chemistryCrystal engineeringchemistry01 natural sciencesBiochemistryIonDioxanesX-rayPolymer chemistryTrifluoroacetic AcidAnion bindingta116N-AlkylammoniumMesylateschemistry.chemical_classificationanion-exchangeIon exchange010405 organic chemistryChemistryOrganic ChemistryGeneral ChemistryResorcinarene3. Good health0104 chemical sciencesCalixarenesTrifluoromethanesulfonateChemistry: An Asian Journal
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New acridinium trifluoromethanesulfonate stacks induced in the presence of organotin(IV) complexes

2013

Abstract Three new crystalline architectures based on acridinium trifluoromethanesulfonate salts [C13H10N]+[CF3SO3]– have been isolated as single crystals from the reaction of the dimeric hydroxo di-n-butylstannane trifluoromethanesulfonato complex [n-Bu2Sn(OH)(H2O)(CF3SO3)]2 (1) with acridine (C13H9N, Acr), in dichloromethane at room temperature. When an equimolar mixture of anthracene (C14H10, Ant) and acridine is initially used, the crystallization of a sandwich-type arrangement occurs, leading to the intercalation of one molecule of anthracene between two acridium trifluoromethanesulfonate salt molecules. In the three X-ray structures reported, the crystal packing involves the contribut…

AnthraceneHydrogen bondStereochemistryGeneral Chemical EngineeringIntercalation (chemistry)General ChemistryCrystal engineeringMedicinal chemistrylaw.inventionchemistry.chemical_compoundchemistrylawAcridineMoleculeCrystallizationTrifluoromethanesulfonateComptes Rendus Chimie
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Organotin(IV) trifluoromethanesulfonates chemistry: Isolation and characterization of a new di-n-butyl derivative presenting a Sn3O3 core

2012

Abstract Reaction of the dimeric hydroxo di-n-butylstannane trifluoromethanesulfonato complex [n-Bu2Sn(OH)(H2O)(CF3SO3)]2 (1) with a mixture of anthracene (C14H10, Ant) and phenazine (C12H8N2, Phz) in dichloromethane at room temperature yielded the novel di-n-butyltin(IV) trifluoromethanesulfonate salt {[n-Bu2Sn(H2O)]2O·n-Bu2Sn(OH)2}(CF3SO3)2 (2), together with the co-crystallization of phenazinium trifluoromethanesulfonate salts ([C12H9N2][CF3SO3], PhzH) collected in the solid state in two distinct self-assembled architectures, 3 and 4, showing π–π stacking interactions, and involving the intercalation of free molecules of phenazine and anthracene, respectively. Complex 2 is a cationic tri…

AnthraceneHydrogen bondStereochemistryPhenazineSupramolecular chemistryCrystal engineeringInorganic Chemistrychemistry.chemical_compoundCrystallographyTrigonal bipyramidal molecular geometrychemistryMaterials ChemistryMoleculePhysical and Theoretical ChemistryTrifluoromethanesulfonateInorganica Chimica Acta
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Composite polymer electrolytes with improved lithium metal electrode interfacial properties: II. Application in rechargeable batteries

1998

The application of a liquid-free, ceramic-added composite polymer electrolyte in a Li/LiMn{sub 2}O{sub 4} rechargeable battery is presented and discussed. As expected by the high stability of the electrolyte toward the lithium metal anode, the battery has promising characteristics in terms of reliability and cyclability.

Battery (electricity)Materials scienceRenewable Energy Sustainability and the EnvironmentInorganic chemistryElectrolyteCondensed Matter PhysicsLithium aluminateEnergy storageSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAnodechemistry.chemical_compoundchemistryChemical engineeringElectrodeMaterials ChemistryElectrochemistryFast ion conductorTrifluoromethanesulfonate
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ChemInform Abstract: Enantioselective Synthesis of Herbertane Sesquiterpenes: Synthesis of (-)-α-Formylherbertenol.

2010

Abstract The synthesis of 4-hydroxy-3-[(1 S )-1,2,2-trimethylcyclopentyl]benzaldehyde [(−)-α-formylherbertenol 1 ], a herbertane-type sesquiterpene isolated from the leafy liverwort Herberta adunca , from β-cyclogeraniol is described. The synthesis is based on the previously described preparation of an enantiopure 1,2,2-trimethylcyclopentane synthon from which the characteristic aromatic moiety of 1 is elaborated, using a Robinson annulation and a palladium-catalysed methoxycarbonylation of an aryl triflate as key synthetic steps. The synthesis of the natural sesquiterpene (−)-α-herbertenol, also a natural sequiterpene, using the same methodology is also described.

Benzaldehydechemistry.chemical_compoundEnantiopure drugChemistryStereochemistryArylSynthonRobinson annulationEnantioselective synthesisGeneral MedicineSesquiterpeneTrifluoromethanesulfonateChemInform
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