Search results for "Catalyst"

showing 10 items of 516 documents

Thiourea Organocatalysts as Emerging Chiral Pollutants: En Route to Porphyrin-Based (Chir)Optical Sensing

2021

Environmental pollution with chiral organic compounds is an emerging problem requiring innovative sensing methods. Amino-functionalized thioureas, such as 2-(dimethylamino)cyclohexyl-(3,5-bis(trifluoromethyl)phenyl)thiourea (Takemoto’s catalyst), are widely used organocatalysts with virtually unknown environmental safety data. Ecotoxicity studies based on the Vibrio fischeri luminescence inhibition test reveal significant toxicity of Takemoto’s catalyst (EC50 = 7.9 mg/L) and its NH2-substituted analog (EC50 = 7.2–7.4 mg/L). The observed toxic effect was pronounced by the influence of the trifluoromethyl moiety. En route to the porphyrin-based chemosensing of Takemoto-type thioureas, their s…

Circular dichroismSupramolecular chemistrychiralitymonitorointiEnvironmental pollutionchiral amineVibrio fischeriQD415-436010402 general chemistryBiochemistry01 natural sciencesMedicinal chemistrysupramolecular chemistrybakteeritAnalytical Chemistry<i>Vibrio</i> <i>fischeri</i>chemistry.chemical_compoundkatalyytitrikkiyhdisteetsupramolekulaarinen kemiaMoiety[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistrythioureaorgaaniset yhdisteetchiral pollutantsTrifluoromethyl010405 organic chemistrytoxicityhost–guest bindingPorphyrin0104 chemical sciencesTakemoto’s catalystcircular dichroismekotoksikologiachemistryThiourea13. Climate action[SDV.TOX.ECO]Life Sciences [q-bio]/Toxicology/Ecotoxicology[SDE.BE]Environmental Sciences/Biodiversity and EcologyChirality (chemistry)porphyrinorganocatalyst
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First-Principles Modelling of N-Doped Co3O4

2018

The project Nr. AP05131211 “First Principles Investigation on Catalytic Properties of N-doped Co3O4” is supported by the Ministry of Education and Science of the Republic of Kazakhstan within the framework of the grant funding for scientific and (or) scientific and technical research for 2018-2020. The authors thank T. Inerbaev and A. Popov for fruitful discussions and valuable suggestions. Yu.M. thanks M.Putnina for the technical assistance in preparation of the manuscript.

Condensed Matter::Quantum GasesMaterials sciencePhysicsQC1-999DopingGeneral EngineeringGeneral Physics and Astronomy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesCondensed Matter::Materials ScienceCo3O4Condensed Matter::SuperconductivityoerPhysics::Atomic and Molecular Clustersco3o4:NATURAL SCIENCES:Physics [Research Subject Categories]OERPhysical chemistryelectrocatalystPhysics::Atomic Physics0210 nano-technology
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Nanostructured Ni Based Anode and Cathode for Alkaline Water Electrolyzers

2019

Owing to the progressive abandoning of the fossil fuels and the increase of atmospheric CO2 concentration, the use of renewable energies is strongly encouraged. The hydrogen economy provides a very interesting scenario. In fact, hydrogen is a valuable energy carrier and can act as a storage medium as well to balance the discontinuity of the renewable sources. In order to exploit the potential of hydrogen it must be made available in adequate quantities and at an affordable price. Both goals can be potentially achieved through the electrochemical water splitting, which is an environmentally friendly process as well as the electrons and water are the only reagents. However, these devices stil…

Control and OptimizationMaterials scienceNanostructureHydrogen020209 energyEnergy Engineering and Power Technologychemistry.chemical_elementNanotechnology02 engineering and technologyElectrocatalystElectrosynthesiselectrocatalystslcsh:Technologynickeliridium oxideHydrogen economySettore ING-IND/17 - Impianti Industriali Meccanicinanostructures0202 electrical engineering electronic engineering information engineeringalkaline electrolyzersElectrical and Electronic EngineeringEngineering (miscellaneous)Energy carrierRenewable Energy Sustainability and the Environmentbusiness.industrylcsh:TOxygen evolutionElectrocatalyst021001 nanoscience & nanotechnologypalladiumcobaltAnodeNanowireSettore ING-IND/23 - Chimica Fisica Applicatachemistrynanowiresni-alloyWater splitting0210 nano-technologybusinessAlkaline electrolyzerfoamEnergy (miscellaneous)Energies
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Multidentate Tetrahydrofurfuryloxide Ligand in a Ziegler−Natta Catalyst Studied by Molecular Modeling

2008

The transition from a generation III Ziegler-Natta catalyst with a monodentate Lewis base to a more modem generation 1V/V system, containing a tetrahydrofuran derivative, the tetrahydrofurturyloxide C 4 H 7 O-CH 2 O - bidentate ligand (THFFO), was studied by means of molecular modeling and DFT calculations. This particular ligand was carefully chosen so that it remained in the titanium coordination sphere in the model active site. With such a constraint, the dual role of tetrahydrofurfuryloxide was identified: it was demonstrated how the presence of this ligand limits the number of isomeric active sites as well as enhances the selectivity of the species that can still exist. The results ind…

Coordination sphereDenticityPolymers and PlasticsbiologyLigandOrganic ChemistryActive siteCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryMaterials Chemistrybiology.proteinLewis acids and basesZiegler–Natta catalystTetrahydrofuranMacromolecules
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ChemInform Abstract: Switchable Palladium-Catalyst Reaction of Bromomethyl Sulfoxides, CO, and N-Nucleophiles: Aminocarbonylation at Csp3versus Oxida…

2013

Pd2(dba)3/ Xantphos-catalyzed coupling of the sulfoxides (I) and (V) with amines and carbon monoxide allows a new and efficient access to amides of type (IV) and (VI).

Coupling (electronics)chemistry.chemical_compoundNucleophileChemistryOxidative carbonylationPolymer chemistryGeneral MedicinePalladium catalystPyrrole derivativesCarbon monoxideChemInform
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POSS-Al-porphyrin-imidazolium cross-linked network as catalytic bifunctional platform for the conversion of CO2 with epoxides

2023

Two heterogeneous catalysts were prepared with the aim of following the promising path of CO2 fixation into epoxides. The synthetic procedure involves a radical copolymerization of an octavinylsilsesquioxane as inorganic core building block and tetrastyrylporphyrin aluminum chloride monomer (TSP-AlCl) in presence (POSS-TSP-AlCl-imiBr) or in absence (POSS-TSP-AlCl) of a bis-vinylimidazolium bromide salt (bis-imiBr), in order to investigate if the bifunctional heterogeneous material can display better catalytic performance than the separate species. All the solids were fully characterized and tested in the synthesis of cyclic carbonates starting from CO2 and several epoxides. The synergic coo…

Cyclic CarbonatesSilsesquioxanesSilsesquioxaneFuel TechnologyBifunctional catalystGeneral Chemical EngineeringOrganic ChemistryEnergy Engineering and Power TechnologySettore CHIM/06 - Chimica OrganicaCyclic CarbonateCarbon Dioxide conversionAl-porphyrinFuel
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Enantiocontrol in the intermolecular cyclopropanation reaction catalyzed by dirhodium(II) complexes with ortho-metalated aryl phosphine ligands

2001

(P) and (M) dirhodium(II) complexes with ortho-metalated aryl phosphines are assessed as chiral catalysts in the enantioselective cyclopropanation of styrenes by ethyl diazoacetate; enantioselectivities up to 91% and up to 87%, respectively, for cis- and trans-2-arylcyclopropanecarboxylates are observed. Barberis, Mario, Mario.Barberis@uv.es ; Lahuerta Peña, Pascual, Pascual.lahuerta@uv.es ; Perez Prieto, Julia, Julia.Perez@uv.es ; Sanau Torrecilla, Mercedes, Mercedes.Sanau@uv.es

CyclopropanationUNESCO::QUÍMICAMedicinal chemistry:QUÍMICA [UNESCO]CatalysisCatalysischemistry.chemical_compoundEthyl diazoacetateMaterials ChemistryOrganic chemistryPhosphine ligandsEnantiocontrol ; Intermolecular cyclopropanation ; Catalyst ; Phosphine ligandsArylIntermolecular forceMetals and AlloysEnantioselective synthesisGeneral ChemistryUNESCO::QUÍMICA::Química macromolecularSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsEnantiocontrolchemistryCeramics and Composites:QUÍMICA::Química macromolecular [UNESCO]CatalystIntermolecular cyclopropanationPhosphine
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Hirālu piridīna organokatalizatoru izstrāde un pielietojums

2015

Maģistra darba ietvaros tika izstrādāta hirālu DMAP organokatalizatoru sintēze. Iegūto organokatalizatoru aktivitāte tika pārbaudīta tetrazola hemiaminālu dinamiskajā kinētiskajā sadalīšanā.

DYNAMIC KINETIC RESOLUTIONTETRAZOLE HEMIAMINALDIAZOTRANSFERĶīmijaCHIRAL DMAP ORGANOCATALYSTS
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DFT analysis of titanium complexes with oxygen-containing bidentate ligands

2003

Strength of the TiO co-ordinate bond in several titanium complexes with bidentate ligands has been investigated by means of DFT. Mutual interaction of particular donors and their influence on Lewis acidity of the central atom have also been studied. The energy of ligand binding ranges from −19 to −454 kJ/mol, depending on the kind of donors. Calculations confirm that a strong donor, alkoxide anion, co-ordinatively saturates the titanium and makes binding of new ligands less exoenergetic. On the contrary, two oxygen atoms of similar donor number do not have much influence on each other. Strength of the TiO bonds in titanium complexes with certain oxygen-containing bidentate ligands has bee…

DenticityLewis baseChemistryStereochemistryProcess Chemistry and TechnologyZiegler–Natta catalystBinding energychemistry.chemical_elementDFTCatalysisCatalysisCrystallographychemistry.chemical_compoundOlefin polymerisationAtomDonor numberAlkoxideLewis acids and basesPhysical and Theoretical ChemistryTitaniumJournal of Molecular Catalysis A-Chemical
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Theoretical study of isomerism in phenoxyimine-based precursors of coordinative olefin polymerization catalysts

2010

Precursors of post-metallocene olefin polymerization catalysts, unlike their predecessors, are usually octahedral transition metal complexes with multidentate ligands. Such ligands may wrap around the central atom in many ways, thus yielding several isomeric species. For a wide range of phenoxyimine (FI) ligands with different substituents, all the theoretically predicted diastereomers of group 4 and 5 complexes are available synthetically. However, only one of the isomers is usually preferred, and this is determined by the nature of the substituents in the FI ligand. The origin and mechanism of such preference has not been completely elucidated. We attempted to describe it quantitatively o…

DenticitySchiff baseLigandStereochemistryProcess Chemistry and TechnologyFI catalystSubstituentDiastereomerDFTCatalysisphenoxyimineCatalysischemistry.chemical_compoundchemistryTransition metalPolymer chemistryDensity functional theoryPhysical and Theoretical Chemistryolefin polymerizationJournal of Molecular Catalysis A-Chemical
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