Search results for "SOLVENT"

showing 10 items of 1395 documents

Ionic liquids/[bmim][N3] mixtures: promising media for the synthesis of aryl azides by SNAr

2008

The nucleophilic aromatic substitution of some activated aryl or heteroaryl halides has been performed in ionic liquid solution, using the 1-butyl-3-methylimidazolium azide as a nucleophile. The reaction course was studied varying the structures of both substrates and ionic liquids. In particular, in the latter case, the reaction of 2-bromo-5-nitrothiophene was carried out in five different ionic liquids ([bmim][BF 4], [bmim][PF 6], [bmim][NTf 2], [bm 2im][NTf 2], and [bmpyrr][NTf 2]). Finally, for all the substrates considered, a comparison with data obtained in MeOH solution in the presence of NaN 3 was also performed. Data collected indicate that in some cases it is possible to obtain ar…

ArylOrganic ChemistryMedicinal chemistryionic liquids aril azides task specific ionic liquidschemistry.chemical_compoundchemistryNucleophileNucleophilic aromatic substitutionIonic liquidNucleophilic substitutionOrganic chemistryMoleculeAzideSolvent effects
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Dressed emitters as impurities

2021

Dressed states forming when quantum emitters or atoms couple to a photonic bath underpin a number of phenomena and applications, in particular dispersive effective interactions occurring within photonic bandgaps. Here, we present a compact formulation of the resolvent-based theory for calculating atom-photon dressed states built on the idea that the atom behaves as an effective impurity. This establishes an explicit connection with the standard impurity problem in condensed matter. Moreover, it allows us to formulate and settle in a model-independent context a number of properties previously known only for specific models or not entirely formalized. The framework is next extended to the cas…

Atom-photon bound states quantum optics waveguide-QEDQC1-999FOS: Physical sciencesContext (language use)ImpurityQuantum mechanicsBound statePhysics::Atomic Physicsquantum opticsElectrical and Electronic EngineeringQuantumResolventCommon emitterPhysicsQuantum Physicsphotonic band-gap materials; quantum optics; waveguide-QEDbusiness.industryphotonic band-gap materialsPhysicsAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsConnection (mathematics)waveguide-qedPhotonicsbusinessQuantum Physics (quant-ph)Biotechnology
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LUA projekts „Universitāšu ieguldījums Latvijas tautsaimniecībā”

2012

2011.gada novembrī – decembrī tika veikta Latvijas universitāšu (Latvijas Universitātes, Rīgas Stradiņa universitātes, Rīgas Tehniskās universitātes, Latvijas Lauksaimniecības universitātes, Liepājas Universitātes un Daugavpils Universitātes) 2006. – 2011.gada absolventu aptauja. Tās ietvaros tika noskaidroti dažādi jautājumi par respondentu iegūto izglītību, plāni par turpmāko izglītošanos, kā arī par absolventu aktivitātēm darba tirgū. Respondenti raksturoja, kāda līmeņa izglītību ir ieguvuši, sniedza detalizētāku informāciju par to, vai ir studējuši pilna laika klātienē, vai studijas ir bijušas par valsts budžeta līdzekļiem, kā arī vai studiju laikā ir izieta prakse.

Augstākā izglītībaStudijasDarba tirgusAbsolventi
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Cellulose‑copper as bio-supported recyclable catalyst for the clickable azide-alkyne [3 + 2] cycloaddition reaction in water.

2018

Abstract Naturally-occurring cellulose has been employed as a bio-support macromolecule for the immobilization of either copper(I) or copper(II) ions in order to click azide and alkyne derivatives in water. Under such a click regime, 1,4-disubstitued-1,2,3-triazoles were obtained regioselectively in excellent yields at room temperature. The reaction work-up is simple and the bio-heterogeneous catalyst that has been fully characterized by AAS, SEM, EDX and FT-IR can be easily separated and reused at least five times without any significant decrease in its activity and selectivity, particularly in the case of the very stable CuI-Cellulose.

Azides123-TriazoleAlkynechemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCatalysisCatalysischemistry.chemical_compoundStructural BiologyPolymer chemistrySpectroscopy Fourier Transform InfraredCelluloseCelluloseMolecular Biologychemistry.chemical_classificationCycloaddition Reaction010405 organic chemistryChemistryWaterGeneral MedicineCopperCycloaddition0104 chemical sciencesAlkynesClick chemistrySolventsClick ChemistryAzideCopperInternational journal of biological macromolecules
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Bile acid–cysteamine conjugates: Structural properties, gelation, and toxicity evaluation

2011

Abstract Design, synthesis, and characterization of six novel bile acid–cysteamine conjugates together with investigation of their structural studies, gelation properties, and preliminary toxicity evaluation, are reported. Solid state properties of selected compounds were studied by means of X-ray diffraction and 13C CPMAS NMR spectroscopy. N-(2-thioethyl)-3α,7α,12α-trihydroxy-5β-cholan-24-amide was shown to exhibit (pseudo)polymorphism, and a single crystal structure of its non-stoichiometric hydrate is reported herein. Cholyl and dehydrocholyl derivatives bearing three functionalities in their steroidal backbone were shown to undergo self-assembly leading to gelation in certain organic so…

BALB 3T3 CellsMagnetic Resonance Spectroscopymedicine.drug_classCysteamineClinical BiochemistryCholic AcidBiochemistryBile Acids and SaltsInhibitory Concentration 50Micechemistry.chemical_compoundEndocrinologyX-Ray DiffractionmedicineAnimalsOrganic chemistryta116Molecular BiologyPharmacologyBile acidUrsodeoxycholic AcidOrganic ChemistryHydrogen BondingNuclear magnetic resonance spectroscopyFibroblastsAmidesCombinatorial chemistrychemistrySolid-state nuclear magnetic resonancePolymorphism (materials science)SolventsLithocholic AcidCysteamineHydrateSingle crystalDeoxycholic AcidConjugateSteroids
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A convenient route for the preparation of the monohydride catalyst trans-[RuCl(H)(dppe)2] (dppe=Ph2PCH2CH2PPh2): improved synthesis and crystal struc…

2013

Abstract A novel and improved room temperature synthesis of the monohydride catalyst trans-[RuCl(H)(dppe)2] complex (1, dppe (1,2-bis(diphenylphosphino)ethane) = Ph2PCH2CH2PPh2) proceeds through oxidation of methanol (the solvent) by the pentacoordinated cis-[RuCl(dppe)2][PF6] complex and t-BuOK as the base is described. Compound 1 was fully characterized by NMR (1H, 13C, 31P), ESI-MS(TOF +), FTIR and elemental analysis. The X-ray structure of 1 was reported for the first time and unambiguously confirms the trans-configuration of the complex.

Base (chemistry)chemistry.chemical_elementHomogeneous catalysisCrystal structure.PhotochemistryMedicinal chemistryRutheniumCatalysisInorganic Chemistrychemistry.chemical_compoundFaculdade de Ciências Exatas e da EngenhariaMaterials ChemistryPhysical and Theoretical ChemistryFourier transform infrared spectroscopyta116Syntethic methdoschemistry.chemical_classificationChemistryHydridesHomogeneous catalisysX-ray crystal structureRutheniumSolventMethanolHydrogenation
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Zur Autoxydation von Polystyrol

1971

Die mit Azoisobuttersauredinitril (AIBN) initiierte Autoxydation von Polystyrol (PS) in Chlorbenzol bei 60°C ist von der Ordnung 0,75, bezogen auf AIBN, und 0,34, bezogen auf PS. Der niedrige Exponent der Polystyrolkonzentration weist neben intermolekularen Wachstumsschritten auf intramolekulare Reaktionsschritte bei der Autoxydation hin. Die bei der Autoxydation am Polystyrol gebildeten Hydroperoxidgruppen zerfallen in Essigsathylester als Losungsmittel mit einer Aktivierungsenthalpie von 19,7 kcal/Mol und einer Aktivierungsentropie von −29 cal/Mol Grad. Das spricht fur einen monomolekularen bifunktionellen Zerfallsmechanismus. Als fluchtige Produkte bei diesem Hydroperoxidzerfall werden P…

BenzaldehydeSolventchemistry.chemical_compoundchemistryChlorobenzenePolymer chemistryEnthalpyPhenolPolystyreneBifunctionalAcetophenoneDie Makromolekulare Chemie
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1,3-Dipolar cycloadditions of electrophilically activated benzonitrile N-oxides. Polar cycloaddition versus oxime formation.

2006

The reactions of electrophilically activated benzonitrile N-oxides (BNOs) toward 3-methylenephthalimidines (MPIs) have been studied using density functional theory (DFT) at the B3LYP/6-31G* level. For these reactions, two different channels allowing the formation of the [3 + 2] cycloadducts and two isomeric (E)- and (Z)-oximes have been characterized. The 1,3-dipolar cycloadditions take place along concerted but highly asynchronous transition states, while formation of the oximes is achieved through a stepwise mechanism involving zwitterionic intermediates. Both reactions are initiated by the nucleophilic attack of the methylene carbon of the MPIs to the carbon atom of the electrophilically…

Benzonitrilechemistry.chemical_compoundchemistryNucleophileStereochemistryOrganic ChemistrySolvent effectsMethylenePhotochemistryTransition stateCycloadditionElectron localization functionNatural bond orbitalThe Journal of organic chemistry
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Chromatographic separation of chlorthalidone enantiomers using β-cyclodextrins as chiral additives

2000

Different beta-cyclodextrins have been tested as chiral additives in the mobile phase for the chromatographic analysis of chlorthalidone enantiomers in a C18 LiChrospher (125 x 4 mm I.D.) column. The effect on enantioresolution of different parameters was studied: composition of the mobile phase (percentage of organic solvent, type of buffer and pH), mobile phase flow-rate, and type and concentration of beta-cyclodextrin. A 25:75 mixture of methanol and 0.1 M phosphate buffer, pH 4, containing 2% triethylamine (v/v), and 12.5 mM beta-cyclodextrin, at a flow-rate of 0.8 ml/min, was found to be the best option for the resolution of chlorthalidone enantiomers. Under such conditions, linear cal…

Beta-Cyclodextrinschemistry.chemical_compoundSpectrophotometrymedicineHumansDiureticsTriethylaminechemistry.chemical_classificationDetection limitCyclodextrinsChromatographyCyclodextrinmedicine.diagnostic_testbeta-CyclodextrinsChlorthalidoneStereoisomerismGeneral ChemistrySolutionschemistrySolventsIndicators and ReagentsSpectrophotometry UltravioletChlorthalidoneMethanolEnantiomermedicine.drugJournal of Chromatography B: Biomedical Sciences and Applications
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Low temperature optical spectroscopy of low-spin ferric hemeproteins

1996

We report the Soret absorption spectra (500-350 nm) of the cyanomet derivatives of human hemoglobin and horse myoglobin, in the temperature range 300-20 K and in two different solvents (65% v/v glycerol-water or 65% v/v ethylene glycol-water). In order to obtain information on stereodynamic properties of active site of the two hemeproteins, we perform an analysis of the band profiles within the framework of electron-vibrations coupling. This approach enables us to single out the various contributions to the spectral bandwidth, such as those arising from non-radiative decay of the excited electronic state (homogeneous broadening) and from the coupling of the electronic transition i) with hig…

Binding SitesAbsorption spectroscopyChemistryIronBiophysicsAnalytical chemistryGeneral MedicineSoft modesAtmospheric temperature rangeSpectral lineMolecular electronic transitionCold TemperatureSpectrophotometrySolventsAnimalsHumansPhysical chemistryHorsesHemeproteinsMetmyoglobinMuscle SkeletalHomogeneous broadeningSpectroscopyOxidation-ReductionMethemoglobin
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