Search results for "LK"

showing 10 items of 8438 documents

Light-Induced Alkylation of (Hetero)aromatic Nitriles in a Transition-Metal-Free C–C-Bond Metathesis

2017

A light-induced C–C-σ-bond metathesis was achieved through transition-metal-free activation of an unstrained C(sp3)–C(sp3)-σ-bond in 1-benzyl-1,2,3,4-tetrahydroisoquinolines. A photoredox-mediated single-electron oxidation of these precursor amines yield radical cations which undergo a homolytic cleavage of a C(sp3)–C(sp3)-σ-bond rather than the well-known α-C–H-scission. The resulting carbon-centered radicals are used in the ipso-substitution of (hetero)aromatic nitriles proceeding through another single-electron transfer-mediated C–C-bond cleavage and formation.

010405 organic chemistryChemistryRadicalOrganic ChemistryAlkylation010402 general chemistryPhotochemistryCleavage (embryo)Metathesis01 natural sciencesBiochemistryMedicinal chemistry0104 chemical sciencesTransition metalYield (chemistry)Light inducedPhysical and Theoretical ChemistryBond cleavageOrganic Letters
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Tetracationic and Tetraanionic Manganese Porphyrins: Electrochemical and Spectroelectrochemical Characterization

2017

International audience; The electrochemistry and spectroelectrochemistry of four tetrapositively charged and two tetranegatively charged porphyrins were characterized in two nonaqueous solvents (dimethyl sulfoxide and N,N-dimethylformamide) containing 0.1 M tetra-n-butylammonium perchlorate. The tetrapositively charged compounds are represented by the tetrapyridylporphyrins [TRPyPM]4+(X-)4, where R is a methyl or [2-[2-(2-methoxy)ethoxy]ethoxy]ethyl group, M = MnIIII, MnIIICl, CuII, or PdII, and X = I- or Cl-. The tetranegatively charged porphyrins are represented by the tetrasulfonato derivatives [TPPSMn(OAc)]4-(NH4+)4 and [TArPSMn(OAc)]4-(NH4+)4, where Ar = 4-O-[2-[2-(2-methoxy)ethoxy]eth…

010405 organic chemistryDimethyl sulfoxidechemistry.chemical_element[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryManganese[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryElectrochemistryPhotochemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundPerchloratechemistry13. Climate actionAlkoxy groupPyridiniumEthyl groupPhysical and Theoretical Chemistry
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Alkali Blues: Blue‐Emissive Alkali Metal Pyrrolates

2019

2-Iminopyrroles [HtBu L, 4-tert-butyl phenyl(pyrrol-2-ylmethylene)amine] are non-fluorescent π systems. However, they display blue fluorescence after deprotonation with alkali metal bases in the solid state and in solution at room temperature. In the solid state, the alkali metal 2-imino pyrrolates, M(tBu L), aggregate to dimers, [M(tBu L)(NCR)]2 (M=Li, R=CH3 , CH(CH3 )CNH2 ), or polymers, [M(tBu L)]n (M=Na, K). In solution (solv=CH3 CN, DMSO, THF, and toluene), solvated, uncharged monomeric species M(tBu L)(solv)m with N,N'-chelated alkali metal ions are present. Due to the electron-rich pyrrolate and the electron-poor arylimino moiety, the M(tBu L) chromophore possesses a low-energy intra…

010405 organic chemistryOrganic ChemistryGeneral ChemistryChromophore010402 general chemistryAlkali metal01 natural sciencesMedicinal chemistryCatalysis0104 chemical scienceschemistry.chemical_compoundMonomerDeprotonationchemistryIntramolecular forceExcited stateMoietyAmine gas treatingChemistry – A European Journal
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Copper-Catalyzed Aerobic Oxidative Alkynylation of 3,4-Dihydroquinoxalin-2-ones

2019

Herein, we described a ligand-free copper-catalyzed aerobic oxidative functionalization of 3,4-dihydroquinoxalin-2(1H)-ones with terminal alkynes using visible-light and oxygen as terminal oxidant to give 3-ethynyl-3,4-dihydroquinoxalin-2(1H)-one, cyclic propargylic amines, in moderate to good yields. Moreover, we demonstrate the versatility of the 3-ethynyl-3,4-dihydroquinoxalin-2(1H)-ones obtained by preparing several 3,4-dihydroquinoxalin-2-one derivatives.

010405 organic chemistryOrganic Chemistrychemistry.chemical_elementOxidative phosphorylation010402 general chemistry01 natural sciencesOxygenCombinatorial chemistryCopperCatalysis0104 chemical sciencesCompostos orgànics SíntesiAlkynylationchemistryCatàlisiCopper catalyzedSurface modificationQuímica orgànica
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The hetero-cubane structures of the heavy alkali metal tert-amyloxides [MOCMe2Et]4 (M = K, Rb, Cs)

2018

A series of alkali metal (Li–Cs) alkoxides of tert-pentanol (1,1-dimethylpropan-1-ol) have been prepared by reaction of the corresponding metal with the alcohol in n-hexane or n-heptane. The compounds were purified by vacuum sublimation and crystallised in n-hexane to produce crystals suitable for single-crystal X-ray diffraction studies. The structures of the potassium, rubidium, and caesium compounds revealed tetrameric units with additional intra- and intermolecular interactions between the metal atom and alkoxide methyl groups, increasing with the size of the metal involved.

010405 organic chemistryPotassiumIntermolecular forcechemistry.chemical_element010402 general chemistryAlkali metal01 natural sciences0104 chemical sciencesRubidiumInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryCubaneCaesiumvisual_artAlkoxidevisual_art.visual_art_mediumDalton Transactions
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Reactions in the presence of irradiated semiconductors: Are they simply photocatalytic?

2018

A generally accepted classification distinguishes semiconductor photocatalysis in type A and type B. The first class comprehends reactions where the primary redox products (radical anions and cations) further evolve giving rise to the final reduced and oxidized species. Type B reactions occur when the primary redox products undergo intermolecular bond formation to addition products. Recently, some photocatalytic reactions have been reported wherein the photocatalytically produced compounds are not the final products. In fact, they react in the solution bulk or catalytically on the surface of the semiconductor with other species thus producing the target compounds. These reactions, hereby re…

010405 organic chemistrybusiness.industryChemistryC-H activation of alkaneOrganic ChemistryPrimary redox product010402 general chemistryPhotochemistry01 natural sciencesIrradiated semiconductor0104 chemical sciencesSemiconductorPhotocatalysisC-O bond formationIrradiationSettore CHIM/07 - Fondamenti Chimici Delle TecnologiebusinessC-N couplingSemiconductor photocatalysi
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A reinvestigation of compound CpMo(PMe3)2(CH3)2: Alkylation by single electron transfer and radical addition?

2001

International audience; The synthesis of the half-sandwich molybdenum(III) diphosphine dimethyl complex CpMo(PMe3)2(CH3)2 has been reinvestigated. The compound was obtained from the corresponding dichloro complex CpMo(PMe3)2Cl2 and methyllithium at low temperatures and isolated as a crystalline product by conducting all operations at temperatures lower than −10 °C. The complex is thermally unstable at room temperature but has been fully characterised by EPR spectroscopy, cyclic voltammetry and X-ray diffraction. The formation reaction is retarded by excess phosphine. On the basis of this and other related observations, a mechanism involving phosphine pre-dissociation followed by single elec…

010405 organic chemistrychemistry.chemical_elementGeneral ChemistryAlkylation010402 general chemistryPhotochemistry01 natural sciences0104 chemical scienceslaw.inventionSingle electronchemistry.chemical_compoundchemistrylawMolybdenumPolymer chemistryMethyllithium[CHIM.COOR]Chemical Sciences/Coordination chemistryCyclic voltammetryElectron paramagnetic resonancePhosphine
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Environmental and biological factors are joint drivers of mercury biomagnification in subarctic lake food webs along a climate and productivity gradi…

2021

Subarctic lakes are getting warmer and more productive due to the joint effects of climate change and intensive land-use practices (e.g. forest clear-cutting and peatland ditching), processes that potentially increase leaching of peat- and soil-stored mercury into lake ecosystems. We sampled biotic communities from primary producers (algae) to top consumers (piscivorous fish), in 19 subarctic lakes situated on a latitudinal (69.0-66.5 degrees N), climatic (+3.2 degrees C temperature and +30% precipitation from north to south) and catchment land-use (pristine to intensive forestry areas) gradient. We first tested how the joint effects of climate and productivity influence mercury biomagnific…

010504 meteorology & atmospheric sciencesBiomagnificationTROPHIC POSITIONmaankäyttö010501 environmental sciencesMETHYLMERCURY01 natural sciencesFood chainBiological FactorsONTARIO LAKESCHAIN STRUCTUREClimate changeympäristömyrkytWaste Management and DisposalLand-useApex predatorTrophic levelkalatStable isotopes2. Zero hungerFRESH-WATEREcologyFishesvesiekosysteemitBIOACCUMULATIONselkärangattomatPollutionSubarctic climateclimate changeProductivity (ecology)Environmental MonitoringFood chain lengthEnvironmental EngineeringFood Chainelohopeachemistry.chemical_elementstable isotopeskasautuminenWHITEFISHland-useEnvironmental ChemistryAnimalsravintoketjutEcosystem1172 Environmental sciences0105 earth and related environmental sciencesfishfood chain lengthLake ecosystemMercury15. Life on landilmastonmuutoksetCHARR SALVELINUS-ALPINUSinvertebratesInvertebratesMercury (element)LakesFishchemistryisotooppianalyysi13. Climate actionEnvironmental scienceMARINEWater Pollutants Chemical
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Diving into exoplanets: Are water seas the most common?

2019

One of the basic tenets of exobiology is the need for a liquid substratum in which life can arise, evolve, and develop. The most common version of this idea involves the necessity of water to act as such a substratum, both because that is the case on Earth and because it seems to be the most viable liquid for chemical reactions that lead to life. Other liquid media that could harbor life, however, have occasionally been put forth. In this work, we investigate the relative probability of finding superficial seas on rocky worlds that could be composed of nine different, potentially abundant, liquids, including water. We study the phase space size of habitable zones defined for those substance…

010504 meteorology & atmospheric sciencesExtraterrestrial EnvironmentMilky WayOrigin of LifePlanets01 natural sciencesAstrobiologyAbundance (ecology)Planet0103 physical sciencesExobiology010303 astronomy & astrophysicsEcosystem0105 earth and related environmental sciencesProbabilityExoseasModels StatisticalHabitable zoneExoplanetsLead (sea ice)WaterAgricultural and Biological Sciences (miscellaneous)ExoplanetTidal lockingSpace and Planetary ScienceSolventsAstrophysics::Earth and Planetary AstrophysicsRelative probabilityCircumstellar habitable zoneGeology
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Explosive eruptive history of Pantelleria, Italy: Repeated caldera collapse and ignimbrite emplacement at a peralkaline volcano

2018

A new, pre-Green Tuff (46 ka) volcanic stratigraphy is presented for the peralkaline Pantelleria Volcano, Italy. New 40Ar/39Ar and paleomagnetic data are combined with detailed field studies to develop a comprehensive stratigraphic reconstruction of the island.We find that the pre-46 ka succession is characterised by eight silicarich peralkaline (trachyte to pantellerite) ignimbrites,many ofwhich blanketed the entire island. The ignimbrites are typically welded to rheomorphic, and are commonly associated with lithic breccias and/or pumice deposits. They record sustained radial pyroclastic density currents fed by lowpyroclastic fountains. The onset of ignimbrite emplacement is typically prec…

010504 meteorology & atmospheric sciencesGeochemistryPyroclastic rockTrachyte010502 geochemistry & geophysics01 natural sciencesPeralkaline rock40Ar/39Ar datingEffusive eruptionGeochemistry and PetrologyPumiceBreccia[SDU.STU.VO]Sciences of the Universe [physics]/Earth Sciences/VolcanologyCalderaEruptive history0105 earth and related environmental sciencesgeographygeography.geographical_feature_categoryIgnimbritesPeralkaline volcanismSettore GEO/07 - Petrologia E PetrografiaSettore GEO/08 - Geochimica E VulcanologiaCaldera collapsePeralkaline volcanism Pantelleria Ignimbrites Caldera collapse Eruptive history 40Ar/39Ar datingGeophysicsVolcano13. Climate actionSeismologyGeologyPantelleria
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