Search results for "synthesi"

showing 10 items of 2904 documents

Co–Co and Co–Fe cyano-bridged pentanuclear clusters based on a methylpyrazinyl-diamine tetradentate ligand: spin crossover and metal substitution eff…

2017

A pentanuclear [CoII3CoIII2] cluster complex has been developed by a solvothermal synthesis. Its highly stable metal-mixed Fe–Co derivatives display robust spin crossover (T1/2 = 268 K) controlled by the degree of substitution.

010405 organic chemistrySolvothermal synthesisSubstitution (logic)General Chemistry010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciences0104 chemical sciencesMetalCrystallographychemistry.chemical_compoundDegree of substitutionchemistrySpin crossovervisual_artDiaminevisual_art.visual_art_mediumCluster (physics)General Materials ScienceTetradentate ligandCrystEngComm
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Magnetostructural correlations in CuII−NC−WV linkage: the case of [CuII(diimine)]2+−[WV(CN)8]3− 0D assemblies

2009

International audience; We report on the syntheses, crystal structures, and magnetic properties of two cyano-bridged molecular assemblies: [CuII(phen)3]2{[CuII(phen)2]2[WV(CN)8]2}(ClO4)2·10H2O (phen = 1,10-phenanthroline) (1) and {[CuII(bpy)2]2[WV(CN)8]} {[CuII(bpy)2][WV(CN)8]}·4H2O (bpy = 2,2′-bipyridyl) (2). Compound 1 consists of cyano-bridged [CuII2WV2]2− molecular rectangles and isolated [CuII(phen)3]2+ complexes. The molecular structure of 2 reveals cyano-bridged trinuclear [CuII2WV]+ and dinuclear [CuIIWV]− ions. Magnetic interactions in 1 are interpreted in terms of the model of a tetranuclear moiety consisting of two ferromagnetic CuII−NC−WV units (J1 = +39(4) cm−1) interacting ant…

010405 organic chemistryStereochemistryChemistryCrystal structureCrystal structureMagnetic response[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry01 natural sciencesAntiferromagnetic coupling0104 chemical sciencesIonInorganic ChemistryCrystallographyFerromagnetismTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYMagnetic propertiesMoleculeMoietyChemical synthesisPhysical and Theoretical ChemistryCyano bridged molecular assembliesDiimine
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Electrochemical and spectroscopic studies of poly(diethoxyphosphoryl)porphyrins

2011

Abstract The synthesis and electrochemical characterization of two related series of porphyrins bearing diethoxyphosphoryl groups are reported. One group of compounds is represented as (T( p -R)PP)M where R = phos = P(O)(OEt) 2 and M = Zn(II) or H 2 while the other is represented as (di( p -R)Pdi(phos)P)M where R = P(O)(OEt) 2 , H or CH 3 and M = Zn(II) or H 2 . Each porphyrin was investigated by electrochemistry and thin-layer spectroelectrochemistry in CH 2 Cl 2 , CDCl 3 , CHCl 3 or PhCN containing tetra- n -butylammonium perchlorate (TBAP) as supporting electrolyte. The highly electron-withdrawing P(O)(OEt) 2 groups lead to easier reductions and harder oxidations than the two comparison …

010405 organic chemistryStereochemistryGeneral Chemical Engineeringchemistry.chemical_elementProtonationZinc010402 general chemistryElectrochemistry01 natural sciencesMedicinal chemistryChemical synthesisPorphyrin0104 chemical sciencesAnalytical ChemistryPerchloratechemistry.chemical_compoundchemistryTetraphenylporphyrinElectrochemistry[CHIM]Chemical SciencesTriphenylphosphine oxideComputingMilieux_MISCELLANEOUS
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Thiourea-Catalyzed Domino Michael–Mannich [3+2] Cycloadditions: A Strategy for the Asymmetric Synthesis of 3,3′-Pyrrolidinyl-dispirooxindoles

2017

The asymmetric synthesis of trifluoromethylated 3,3′-pyrrolidinyl-dispirooxindole derivatives with four contiguous stereogenic centers, including two vicinal spiro-stereocenters, is described. Employing a bifunctional thiourea catalyst, a domino Michael–Mannich [3+2] cycloaddition occurs readily between isatin ketimines and isatin-derived enoates with good yields and very high stereoselectivities, providing a direct entry to the title compounds of potential medical value.

010405 organic chemistryStereochemistryIsatinOrganic ChemistryEnantioselective synthesis010402 general chemistry01 natural sciencesCombinatorial chemistryCycloadditionDomino0104 chemical sciencesStereocenterchemistry.chemical_compoundchemistryCascade reactionThioureaOrganocatalysisSynlett
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Organocatalytic Asymmetric Synthesis of 2,3′-Connected Bis-Indolinones by Mannich Reactions of N-Acetylindolin-3-ones with Isatin N-Boc Ketimines

2017

A highly diastereo- and enantioselective Mannich reaction of N-acetylindolin-3-ones with isatin N-Boc ketimines to form 2,3′-connected bis-indolinones is developed employing a low loading of a readily available bifunctional thiourea catalyst. The asymmetric synthesis connects two indolinones via a vic-diamine unit and generates two neighboring stereocenters.

010405 organic chemistryStereochemistryIsatinOrganic ChemistryEnantioselective synthesis010402 general chemistry01 natural sciencesMedicinal chemistryCatalysis0104 chemical sciencesStereocenterchemistry.chemical_compoundchemistryThioureaOrganocatalysisDiamineBifunctionalMannich reactionSynthesis
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Catalytic enantioselective aza-Reformatsky reaction with seven-membered cyclic imines dibenzo[b,f][1,4]oxazepines

2017

A catalytic enantioselective aza-Reformatsky reaction is reported with cyclic dibenzo[b,f][1,4]oxazepines and ethyl iodoacetate leading to the synthesis of chiral ethyl 2-(10,11-dihydrodibenzo[b,f][1,4]oxazepin-11-yl)acetate derivatives with excellent yields and high enantioselectivities (up to 98% yield and 97 : 3 er) using a readily available diaryl prolinol L4 as the chiral ligand and Me2Zn as the zinc source under an air atmosphere. Furthermore, different transformations were carried out with the corresponding chiral β-amino esters, preserving in all cases the optical purity.

010405 organic chemistryStereochemistryOrganic ChemistryEthyl iodoacetateChiral ligandEnantioselective synthesis010402 general chemistry01 natural sciences0104 chemical sciencesCatalysisProlinolReaccions químiqueschemistry.chemical_compoundchemistryYield (chemistry)Reformatsky reactionEnantiomeric excessQuímica orgànica
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Catalytic Asymmetric Reactions Involving the Seven-Membered Cyclic Imine Moieties Present in Dibenzo[b,f][1,4]oxazepines

2017

The dibenzo[b,f][1,4]oxazepine scaffold is a privileged structure in medicinal chemistry that displays a wide variety of biological and pharmacological activities. However, catalytic asymmetric methodologies for the synthesis of chiral dibenzo[b,f][1,4]oxazepine derivatives are scarce in the literature. This microreview presents an overview of enantioselective reactions in which these cyclic seven-membered imines are used as electrophiles, including their substrate scope, limitations and application to the synthesis of related compounds.

010405 organic chemistryStereochemistryOrganic ChemistryImineEnantioselective synthesisSubstrate (chemistry)010402 general chemistry01 natural sciences0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryElectrophileOxazepinePhysical and Theoretical ChemistryDibenzoxazepinesEuropean Journal of Organic Chemistry
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Linking photosynthesis and sun-induced fluorescence at sub-daily to seasonal scales

2018

Abstract Due to its close link to the photosynthetic process, sun-induced chlorophyll fluorescence (F) opens new possibilities to study dynamics of photosynthetic light reactions and to quantify CO2 assimilation rates. Although recent studies show that F is linearly related to gross primary production (GPP) on coarse spatial and temporal scales, it is argued that this relationship may be mainly driven by seasonal changes in absorbed photochemical active radiation (APAR) and less by the plant light use efficiency (LUE). In this work a high-resolution spectrometer was used to continuously measure red and far-red fluorescence and different reflectance indices within a sugar beet field during t…

010504 meteorology & atmospheric sciencesEconomicsPhotochemical reflectance index0211 other engineering and technologiesEddy covarianceGrowing seasonSoil Science02 engineering and technologyPhotochemical Reflectance IndexPhotosynthesisAtmospheric sciences01 natural sciencesFluorescence yieldSun-induced chlorophyll fluorescencemedicineddc:550Computers in Earth SciencesChlorophyll fluorescenceBiology021101 geological & geomatics engineering0105 earth and related environmental sciencesRemote sensingLight use efficiencyPhysicsDiurnal temperature variationPrimary productionGeologySeasonalitymedicine.diseaseChemistryEngineering sciences. Technology
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Remote sensing of solar-induced chlorophyll fluorescence (SIF) in vegetation: 50 years of progress

2019

Remote sensing of solar-induced chlorophyll fluorescence (SIF) is a rapidly advancing front in terrestrial vegetation science, with emerging capability in space-based methodologies and diverse application prospects. Although remote sensing of SIF – especially from space – is seen as a contemporary new specialty for terrestrial plants, it is founded upon a multi-decadal history of research, applications, and sensor developments in active and passive sensing of chlorophyll fluorescence. Current technical capabilities allow SIF to be measured across a range of biological, spatial, and temporal scales. As an optical signal, SIF may be assessed remotely using high-resolution spectral sensors in …

010504 meteorology & atmospheric sciencesFIS/06 - FISICA PER IL SISTEMA TERRA E PER IL MEZZO CIRCUMTERRESTRE0208 environmental biotechnologySoil ScienceReview02 engineering and technologyPhotochemical Reflectance Index01 natural sciencesArticleGEO/11 - GEOFISICA APPLICATASIF retrieval methodsRadiative transfer modellingRadiative transfer910 Geography & travelComputers in Earth SciencesChlorophyll fluorescence1111 Soil Science1907 GeologyAirborne instruments0105 earth and related environmental sciencesRemote sensingStress detectionGEO/12 - OCEANOGRAFIA E FISICA DELL'ATMOSFERA1903 Computers in Earth SciencesPrimary productionGeologyVegetationPassive optical techniquesField (geography)020801 environmental engineeringGEO/10 - GEOFISICA DELLA TERRA SOLIDA10122 Institute of GeographySun-induced fluorescenceRemote sensing (archaeology)Sun-induced fluorescence Steady-state photosynthesis Stress detection Radiative transfer modelling SIF retrieval methods. Satellite sensors Airborne instruments Applications Terrestrial vegetation Passive optical techniques. ReviewApplicationsTerrestrial vegetationEnvironmental scienceSatelliteSteady-state photosynthesisSatellite sensors
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Matter Mixing in Aspherical Core-collapse Supernovae: Three-dimensional Simulations with Single Star and Binary Merger Progenitor Models for SN 1987A

2019

We perform three-dimensional hydrodynamic simulations of aspherical core-collapse supernovae focusing on the matter mixing in SN 1987A. The impacts of four progenitor (pre-supernova) models and parameterized aspherical explosions are investigated. The four pre-supernova models include a blue supergiant (BSG) model based on a slow merger scenario developed recently for the progenitor of SN 1987A (Urushibata et al. 2018). The others are a BSG model based on a single star evolution and two red supergiant (RSG) models. Among the investigated explosion (simulation) models, a model with the binary merger progenitor model and with an asymmetric bipolar-like explosion, which invokes a jetlike explo…

010504 meteorology & atmospheric sciencesSupergiant starAstrophysics::High Energy Astrophysical PhenomenaBinary numberchemistry.chemical_elementNeutron starFOS: Physical sciencesHydrodynamical simulationAstrophysicsAstrophysics::Cosmology and Extragalactic Astrophysics01 natural sciencesSettore FIS/05 - Astronomia E Astrofisica0103 physical sciencesCore-collapse supernovaeAstrophysics::Solar and Stellar AstrophysicsRed supergiant010303 astronomy & astrophysicsMixing (physics)HeliumStellar evolutionary modelSolar and Stellar Astrophysics (astro-ph.SR)Astrophysics::Galaxy Astrophysics0105 earth and related environmental sciencesLine (formation)PhysicsHigh Energy Astrophysical Phenomena (astro-ph.HE)Astronomy and AstrophysicsSupernova dynamicSupernovaNeutron starchemistryAstrophysics - Solar and Stellar AstrophysicsSpace and Planetary ScienceExplosive nucleosynthesisSupergiantAstrophysics - High Energy Astrophysical Phenomena
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