Search results for "deriva"

showing 10 items of 1423 documents

Determination of alcohols in essential oils by liquid chromatography with ultraviolet detection after chromogenic derivatization

2013

Abstract An HPLC-UV method to determine compounds having a hydroxyl functional group in plant essential oils is developed. The sample is diluted with 1,4-dioxane and the analytes are derivatized with phthalic anhydride. The derivatives (phthalates hemiesters) are separated on a C8 column using an acetonitrile (ACN)/water gradient. Separation conditions were optimized using the DryLab® method development software. For the alcohols and phenols present in mint and rose essential oils, optimization led to a ca. 40 min gradient time and a column temperature of 8 °C. The alcohol and its derivatives were identified using HPLC with mass spectrometry (MS) detection. A large sensitivity enhancement w…

AlcoholRosaMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrylaw.inventionchemistry.chemical_compoundLimit of DetectionlawOils VolatileFlame ionization detectorPhenolsDerivatizationDetection limitPhthalic anhydrideChromatographyOrganic ChemistryTemperatureReproducibility of ResultsGeneral MedicinechemistryAlcoholsPhthalic AnhydridesSpectrophotometry UltravioletChromatography LiquidMenthaJournal of Chromatography A
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Synthesis, characterization of diorganotin(IV) complexes of N-(2-hydroxyarylidene)aminoacetic acid and antitumour screening in vivo in ehrlich ascite…

2001

Some new diorganotin(IV) complexes have been prepared by reacting potassium N-(2-hydroxyarylidene)aminoacetate with R2SnCl2(R = Me,nBu,Ph). The complexes have been characterized by 1H,13C,119Sn NMR, IR and 119mSn Mössbauer spectroscopic techniques in combination with elemental analysis. In the solid state, the complexes possess penta- and hexa-coordinated tin centres. The hexa-coordinated tin complexes were found to dissociate in solution, giving rise to penta-coordinated species as revealed by 119Sn NMR spectroscopy. Antitumour screening in vivo of the complexes L4snPh2,L4SnPh2· Ph3SnCl and L4SntBU2·t Bu2SnCl2 (L4 = N-(2-hydroxyacetophenone)aminoacetate) is also reported. Copyright © 2001 …

AldiminesynthesisStereochemistryMossbauer spectroscopyInfrared spectroscopyAntitumour activityanimal cellantineoplastic activitydissociationChemical synthesisMedicinal chemistryEhrlich ascites tumor cellEhrlich ascites carcinomaInorganic Chemistryin vivo studychemistry.chemical_compoundAcetic acidOrganotinmalecomplex formationorganotin compoundcontrolled studyCarboxylateinfrared spectroscopyEhrlich ascites carcinoma cellmouseglycine derivativenuclear magnetic resonance spectroscopychemistry.chemical_classificationSchiff basenonhumananimal modelarticleGeneral ChemistryNuclear magnetic resonance spectroscopysolid stateNMRAmino acidchemistryreaction analysiSettore CHIM/03 - Chimica Generale E InorganicaIRSchiff baseschemical analysi
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On the critical behavior for time-fractional pseudo-parabolic type equations with combined nonlinearities

2022

AbstractWe are concerned with the existence and nonexistence of global weak solutions for a certain class of time-fractional inhomogeneous pseudo-parabolic-type equations involving a nonlinearity of the form $|u|^{p}+\iota |\nabla u|^{q}$ | u | p + ι | ∇ u | q , where $p,q>1$ p , q > 1 , and $\iota \geq 0$ ι ≥ 0 is a constant. The cases $\iota =0$ ι = 0 and $\iota >0$ ι > 0 are discussed separately. For each case, the critical exponent in the Fujita sense is obtained. We point out two interesting phenomena. First, the obtained critical exponents are independent of the fractional orders of the time derivative. Secondly, in the case $\iota >0$ ι > 0 , we show that the gradie…

Algebra and Number TheoryCaputo fractional derivativecritical exponentSettore MAT/05 - Analisi Matematicapseudo-parabolic type equationglobal weak solutionAnalysiscombined nonlinearitie
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Functional Derivative Approach

2001

Let us now leave the path integral formalism temporarily and reformulate operatorial quantum mechanics in a way which will make it easy later on to establish the formal connection between operator and path integral formalism. Our objective is to introduce the generating functional into quantum mechanics. Naturally we want to generate transition amplitudes. The problem confronting us is how to transcribe operator quantum mechanics as expressed in Heisenberg’s equation of motion into a theory formulated solely in terms of c-numbers. This can be achieved either by Schwinger’s action principle or with the aid of a generation functional defined as follows:

AlgebraFormalism (philosophy of mathematics)Computer sciencePath integral formulationEquations of motionFunctional derivative
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Initial Data for Non-Linear Evolution Equations and Differentiable Vectors of Group Representations

1995

Regularity properties of non-linear Lie algebra representations are defined. These properties are satisfied in examples given by evolution equations. We prove that this regularity implies that the set of C ∞ vectors for the non-linear group representation obtained by integration of the Lie algebra representation coincide with the set of C ∞ vectors of the linear part (the order one term) of this group representation.

AlgebraNonlinear systemLie algebra representationLie algebraDifferentiable functionWeak derivativeGroup representationMathematics
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The role of virtual work in Levi-Civita's parallel transport

2015

The current literature on history of science reports that Levi-Civita’s parallel transport was motivated by his attempt to provide the covariant derivative of the absolute differential calculus with a geometrical interpretation (For instance, see Scholz in The intersection of history and mathematics, Birkhauser, Basel, pp 203–230, 1994, Sect. 4). Levi-Civita’s memoir on the subject was explicitly aimed at simplifying the geometrical computation of the curvature of a Riemannian manifold. In the present paper, we wish to point out the possible role implicitly played by the principle of virtual work in Levi-Civita’s conceptual reasoning to formulate parallel transport.

AlgebraRicci calculusCurrent (mathematics)IntersectionParallel transportComputer scienceCalculusVirtual workRiemannian manifoldCurvatureCovariant derivativePAMM
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Bis(3,5-dimethylpyrazol-1-ato) zirconium complexes as precursors for ethylene polymerisation upon activation with MAO: Syntheses, characterisation an…

2007

Abstract The bis(3,5-dimethylpyrazol-1-ato) zirconium complex [Zr(η2-3,5-Me2Pz)2(NMe2)2(NHMe2)2] (2) is obtained by treatment of [Zr(NMe2)4] with 2 equiv. of 3,5-dimethylpyrazole 1. The reaction of the [ZrCl4(THF)2] adduct with 2 equiv. of the potassium salt of 1 affords the dichloro derivative [Zr(η2-3,5-Me2Pz)2Cl2]n (3), while reaction with 4.1 equiv. of 1 in the presence of 2.1 equiv. of NEt3 affords the dichloro pyrazole adduct [Zr(η2-3,5-Me2Pz)2Cl2(η1-3,5-Me2PzH)2] (4). Treatment of [Zr(CH2Ph)4] with 2 equiv. of 1 gives the dibenzyl complex [Zr(η2-3,5-Me2Pz)2(CH2Ph)2] (5) via alkane elimination. Compound 4 presents fluxional behaviour in CDCl3 solution, which was studied and quantified…

Alkanechemistry.chemical_classificationZirconiumInorganic chemistrychemistry.chemical_elementSalt (chemistry)PyrazoleMedicinal chemistryAdductInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryProton NMRMoleculePhysical and Theoretical ChemistryDerivative (chemistry)Polyhedron
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A multifunctional bioconjugate module for versatile photoaffinity labeling and click chemistry of RNA

2011

A multifunctional reagent based on a coumarin scaffold was developed for derivatization of naive RNA. The alkylating agent N3BC [7-azido-4-(bromomethyl)coumarin], obtained by Pechmann condensation, is selective for uridine. N3BC and its RNA conjugates are pre-fluorophores which permits controlled modular and stepwise RNA derivatization. The success of RNA alkylation by N3BC can be monitored by photolysis of the azido moiety, which generates a coumarin fluorophore that can be excited with UV light of 320 nm. The azidocoumarin-modified RNA can be flexibly employed in structure-function studies. Versatile applications include direct use in photo-crosslinking studies to cognate proteins, as dem…

Alkylating AgentsAzidesFluorophoreUltraviolet RaysPhotoaffinity LabelsPhotoaffinity LabelsBiologyMass Spectrometrychemistry.chemical_compoundCoumarinsGeneticsheterocyclic compoundsDerivatizationFluorescent DyesPhotoaffinity labelingRNANucleosidesCombinatorial chemistrychemistryBiochemistryTransfer RNASynthetic Biology and ChemistryClick chemistryRNAClick ChemistryAzideChromatography LiquidNucleic Acids Research
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Organocatalytic enantioselective functionalization of indoles in the carbocyclic ring with cyclic imines

2019

[EN] An organocatalytic enantioselective functionalization in the carbocyclic ring of indoles with benzoxathiazine 2,2-dioxides is described using a quinine-derived bifunctional organocatalyst. This aza-Friedel-Crafts reaction provides 4-indolyl, 5-indolyl and 7-indolyl sulfamidate derivatives in good yields (up to 99%) and with moderate to high enantioselectivities (up to 86% ee).

Alkylation02 engineering and technologyAlkylation010402 general chemistryRing (chemistry)01 natural sciencesHydroxyindolesCatalysisKetiminesReaccions químiqueschemistry.chemical_compoundMaterials ChemistryFriedel-Crafts reactionBifunctionalFriedel–Crafts reactionConstructionAsymmetric-SynthesisChemistryInhibitorsEnantioselective synthesisGeneral Chemistry021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesFISICA APLICADASurface modification0210 nano-technologyQuímica orgànicaDerivatives
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Synthesis of borylindenides. Complexes with iron and rhenium moieties

1999

Abstract Borylation of lithium indenide with BBrMe 2 gives the allylic 1-indenyl derivative (1-Ind)BMe 2 ( 1c ) together with the bis-allylic connected species (1-Ind) 2 BMe ( 3 ) and with BCl i Pr 2 , the allylic 1-indenyl (1-Ind)B i Pr 2 ( 1d ); the latter, with Et 3 N or Py added, rearranges to the vinylic 3-indenyl isomer (3-Ind)B i Pr 2 ( 2d ). The disubstituted indene C 9 H 6 Ind(SiMe 3 )B(O 2 C 2 Me 4 ) ( 5 ) was prepared from Li[C 9 H 6 B(O 2 C 2 Me 4 )] ( 4b ) and Me 3 SiCl. Both (1-Ind)BMe 2 and (1-Ind)B i Pr 2 readily undergo metalation when treated with LiTMP or LiInd to give pure 1-borylindenides Li(C 9 H 6 BMe 2 ) ( 4c ) and Li(C 9 H 6 B i Pr 2 ) ( 4d ). A barrier to internal …

Allylic rearrangementMetalationOrganic Chemistrychemistry.chemical_elementBoranesRheniumBiochemistryBorylationMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryOrganic chemistryLithiumPhysical and Theoretical ChemistryIndeneDerivative (chemistry)Journal of Organometallic Chemistry
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