Search results for "GAN"

showing 10 items of 55108 documents

Advances in photochemical and electrochemical incorporation of sulfur dioxide for the synthesis of value-added compounds.

2021

Organic photochemistry and electrochemistry currently receive tremendous attention in organic synthesis as both techniques enable the reagent-less activation of organic molecules without using expensive and hazardous redox reagents. The incorporation of SO2 into organic molecules is a relatively modern research topic, which likewise gains immense popularity since the discovery of the SO2 surrogate DABSO. Sulfur-containing organic molecules are omnipresent in pharmaceuticals and agrochemicals. This review covers the recent progress in electrochemical and photochemical methodologies for the incorporation and uses of SO2 in the synthesis of value-added compounds. Additionally, different work t…

010405 organic chemistryChemistryMechanistic organic photochemistryMetals and AlloysGeneral Chemistry010402 general chemistryPhotochemistryElectrochemistrycomplex mixtures01 natural sciencesRedoxCatalysisrespiratory tract diseases0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOrganic moleculeschemistry.chemical_compoundMaterials ChemistryCeramics and CompositesOrganic synthesisSulfur dioxideChemical communications (Cambridge, England)
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A Molecular Electron Density Theory Study of the Role of the Copper Metalation of Azomethine Ylides in [3 + 2] Cycloaddition Reactions.

2018

The copper metalation of azomethine ylides (AYs) in [3 + 2] cycloaddition (32CA) reactions with electron-deficient ethylenes has been studied within the Molecular Electron Density Theory (MEDT) at the MPWB1K/6-311G(d,p) level, in order to shed light on the electronic effect of the metalation in the course of the reaction. Analysis of the Conceptual Density Functional Theory reactivity indices indicates that the metalation of AYs markedly enhances the nucleophilicity of these species given the anionic character of the AY framework. These 32CA reactions take place through stepwise mechanisms characterized by the formation of a molecular complex. Both nonmetalated and metalated 32CA reactions …

010405 organic chemistryChemistryMetalationOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesMedicinal chemistryCycloaddition0104 chemical sciencesNucleophileElectronic effectSingle bondDensity functional theoryReactivity (chemistry)The Journal of organic chemistry
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Leaded Bronze: An Innovative Lead Substitute for Cathodic Electrosynthesis

2017

010405 organic chemistryChemistryMetallurgychemistry.chemical_elementengineering.material010402 general chemistryElectrosynthesis01 natural sciencesCopperCatalysis0104 chemical sciencesCathodic protectionLead (geology)ElectrochemistryengineeringBronzeChemElectroChem
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Photoswitching of the antiferromagnetic coupling in an oxamato-based dicopper(ii) anthracenophane

2011

Thermally reversible photomagnetic (ON/OFF) switching behavior has been observed in a dinuclear oxamatocopper(ii) anthracenophane upon UV light irradiation and heating; the two CuII ions (SCu = 1/2) that are antiferromagnetically coupled in the dicopper(ii) metallacyclic precursor (ON state) become uncoupled in the corresponding [4+4] photocycloaddition product (OFF state), as substantiated from both experimental and theoretical studies. © 2011 The Royal Society of Chemistry.

010405 organic chemistryChemistryMetals and AlloysLight irradiation[CHIM.MATE]Chemical Sciences/Material chemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysisAntiferromagnetic coupling0104 chemical sciences3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonCrystallographyMaterials ChemistryCeramics and CompositesChemical Communications
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Encapsulation and solid state sequestration of gases by calix[6]arene-based molecular containers

2017

Two calix[6]arene-based molecular containers were synthesized in high yields. These containers can encapsulate small guests through a unique "rotating door" complexation process. The sequestration of greenhouse gases is clearly demonstrated. They can be stored in the solid state for long periods and released via dissolution of the inclusion complex.

010405 organic chemistryChemistryMetals and AlloysSolid-stateNanotechnologymolekyylitGeneral Chemistryhiilensidonta010402 general chemistry01 natural sciencescarbon sequestrationCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical engineeringMaterials ChemistryCeramics and CompositesmoleculesDissolutionta116Chemical Communications
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Self-assembly of M4L4tetrahedral cages incorporating pendant PS and PSe functionalised ligands

2019

Herein, the synthesis of metal–organic tetrahedral cages featuring flexible thio- and selenophosphate-based ligands is described. The cages were prepared by sub-component self-assembly of AP(OC6H4NH2-4)3 (A = S, Se) or SP(SC6H4NH2-4)3, 2-pyridinecarboxaldehyde, and either Fe[BF4]2 or Co[BF4]2. Preliminary host–guest studies into the ability of the pendant PS and PSe groups to interact with suitable substrates will be discussed.

010405 organic chemistryChemistryMetals and AlloysThio-General Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPolymer chemistryMaterials ChemistryCeramics and CompositesTetrahedronSelf-assemblyChemical Communications
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Structure effects induced by high mechanical compaction of STAM-17-OEt MOF powders

2021

Financial support by PJ-RIC-FFABR_2017 and the EPSRC grant EPSRC industrial CASE award (grant EP/N50936X/1) are acknowledged. The research programme Nanoporous materials (P1-0021) financially supported by Slovenian Research Agency (ARRS) is acknowledged as well. Metal-organic frameworks (MOFs) are promising materials for many potential applications, spacing from gas storage to catalysis. However, the powder form of which they are generally made is not suitable, mainly because of the low packing density. Powder compaction is therefore necessary, but also challenging because of their typical mechanical fragility. Indeed, generally, they undergo irreversibly damages upon densification processe…

010405 organic chemistryChemistryNanoporousCompactionNanotechnologyFlexible MOFs3rd-DASMetal-organic frameworks010402 general chemistryMOF stabilityQD Chemistry01 natural sciencesMOF tableting0104 chemical sciencesInorganic ChemistryQDMOF TabletingEPR spectroscopy
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Enhanced NiO Dispersion on a High Surface Area Pillared Heterostructure Covered by Niobium Leads to Optimal Behaviour in the Oxidative Dehydrogenatio…

2020

[EN] A Nb-containing siliceous porous clay heterostructure (PCH) with Nb contents from 0 to 30 wt %) was prepared from a bentonite and used as support in the preparation of supported NiO catalysts with NiO loading from 15 to 80 wt %. Supports and NiO-containing catalysts were characterised by several physicochemical techniques and tested in the oxidative dehydrogenation (ODH) of ethane. The characterisation studies on Nb-containing supports showed the presence of well-anchored Nb(5+)species without the formation of Nb(2)O(5)crystals. High dispersion of nickel oxide with low crystallinity was observed for the Nb-containing PCH supports. In addition, when NiO is supported on these Nb-containi…

010405 organic chemistryChemistryNiobiumOrganic ChemistryNon-blocking I/OSupported catalystsNiobiumchemistry.chemical_elementHeterojunctionGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesNickelNickelPorous heterostructuresPhysical chemistryDehydrogenationDehydrogenationDispersion (chemistry)Chemistry - A European Journal
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Synthesis of 2-Aminothiazole Derivatives in Easy Two-Step, One-Pot Reaction

2018

010405 organic chemistryChemistryOne pot reactionOrganic ChemistryTwo step2-aminothiazole010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesJournal of Heterocyclic Chemistry
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Reactivity of [1,2,3]Triazolo[1,5-a]pyridines as 1,3-dipoles

2016

Abstract We have studied the reactions between [1,2,3]Triazolo[1,5- a ]pyridines 1a,b,c and electron-deficient ethylenes in different conditions. Compounds 1a and 1b react with ethyl propiolate, and dimethyl acetylene dicarboxylate giving a new class of biaryl compounds pyridyl pyrazoles, and with ethyl acrylate giving pyridyl cyclopropanes. Compound 1c did not give any product in the studied conditions. A proposal of mechanism of these reactions is done in which the triazolopyridines act as 1,3-dipoles giving 1,3-dipolar cycloadditions.

010405 organic chemistryChemistryOrganic Chemistry010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesEthyl propiolatechemistry.chemical_compoundAcetyleneDrug DiscoveryPolymer chemistryEthyl acrylateReactivity (chemistry)Tetrahedron
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