Search results for "kinetics"

showing 10 items of 2224 documents

Polysaccharide/polyaminoacid composite scaffolds for modified DNA release.

2009

Abstract In this work composite polymeric films or sponges, based on hyaluronic acid (HA) covalently crosslinked with α,β-poly(N-2-hydroxyethyl)(2-aminoethylcarbamate)- d , l -aspartamide (PE), have been prepared and characterized as local gene delivery systems. In particular, HA/PE scaffolds have been loaded with PE/DNA interpolyelectrolyte complexes, employing PE as a macromolecular crosslinker for HA and as a non-viral vector for DNA. In vitro studies showed that HA/PE films and sponges have high compatibility with human dermal fibroblasts and they give a sustained DNA release, whose trend can be easily tailored by varying the crosslinking ratio between HA and PE. Electrophoresis analysi…

StereochemistryMelanoma ExperimentalPharmaceutical ScienceHyaluronoglucosaminidaseElectrophoretic Mobility Shift Assaymacromolecular substancesBiologyGene deliveryTransfectionchemistry.chemical_compoundMiceTissue engineeringHyaluronic acidPolyaminesCOMPOSITE SCAFFOLD SCAFFOLD AMINOACID DNA RELEASE.AnimalsHumansHyaluronic AcidAspartameCells CulturedMolecular StructureGenetic transfertechnology industry and agricultureBiological TransportTransfectionDNAFibroblastsIn vitroKineticsCross-Linking ReagentschemistrySolubilitySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoNucleic Acid ConformationDNAMacromoleculeNuclear chemistryInternational journal of pharmaceutics
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Rotational Isomerism in Acetic Acid: The First Experimental Observation of the High-Energy Conformer

2003

The high-energy conformer of acetic acid (cis-AA) is produced in an Ar matrix by vibrational excitation of the OH stretching overtone of the ground conformational state (trans-AA). IR-absorption spectroscopy provides a clear identification of the reaction product. cis-AA converts back to trans-AA in a time scale of minutes at 8 K by tunneling. http://dx.doi.org/10.1021/ja038341a

StereochemistryOvertoneMolecular ConformationInfrared spectroscopy010402 general chemistry01 natural sciencesBiochemistryCatalysisAcetic acidchemistry.chemical_compoundColloid and Surface ChemistryIsomerismAb initio quantum chemistry methods0103 physical sciencesSpectroscopy Fourier Transform InfraredSpectroscopyConformational isomerismAcetic Acid010304 chemical physicsChemistryMatrix isolationGeneral Chemistry3. Good health0104 chemical sciencesKineticsModels ChemicalPhysical chemistryExcitation
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Are there dynamical effects in enzyme catalysis? Some thoughts concerning the enzymatic chemical step.

2015

Highlights • The possible role of enzymatic reaction dynamical effects is examined. • Solution reactions usefully inform the issue of dynamical effects in enzymes. • Division into regions containing and away from the transition state is important. • Motions in passage to/from the transition state need not lead to dynamical effects. • Transition State Theory is usually a reasonable description of enzyme kinetics.

StereochemistryProtein ConformationBiophysicsBiochemistryModels BiologicalVibrationArticleEnzyme catalysisDiffusionTransition state theoryTransition State TheoryEscherichia coli[CHIM]Chemical SciencesStatistical physicsMolecular BiologyQuantumNuclear motionChemistryQuantitative Biology::Molecular Networksdigestive oral and skin physiologyEnzyme catalysisEnzymesEnzyme ActivationKineticsTetrahydrofolate DehydrogenaseDynamical effectsBiocatalysisQuantum TheoryTetrahydrofolate dehydrogenaseProtonsArchives of biochemistry and biophysics
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Cooperative effects on the HS→LS relaxation in the [Fe(ptz)6](BF4)2 spin-crossover system

1992

Abstract The high-spin to low-spin (HS→LS) relaxation in the [Fe(ptz) 6 ](BF 4 ) 2 spin-crossover system deviates strongly from first-order kinetics because of cooperative effects of elastic origin. The shift in horizontal and vertical displacement of the potential wells of the initial and final state relative to each other due to the build-up of an “internal” pressure is estimated from spectroscopic measurements. The HS→LS relaxation as such is described by the theory of nonadiabatic multiphonon relaxation in the strong-coupling limit, with a Huang—Rhys factor S ≈ 45 which is much larger than the reduced energy gap p . The sigmoidal relaxation curves in [Fe(ptz) 6 ](BF 4 ) 2 result when a …

StereochemistrySpin crossoverBand gapChemistryddc:540KineticsGeneral Physics and AstronomyRelaxation (physics)Physical and Theoretical ChemistryMolecular physicsLIESSTDisplacement (vector)Chemical Physics Letters
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The mechanism of hydrolysis of beta-glycerophosphate by kidney alkaline phosphatase.

1975

1. To identify the functional groups that are involved in the conversion of β-glycerophosphate by alkaline phosphatase (EC 3.1.3.1) from pig kidney, the kinetics of alkaline phosphatase were investigated in the pH range 6.6-10.3 at substrate concentrations of 3 μM-30 mM. From the plots of log ṼH+ against pH and log ṼH+/KH+m against pH one functional group with pK = 7.0 and two functional groups with pK = 9.1 were identified. These groups are involved in substrate binding. Another group with pK = 8.8 was found, which in its unprotonated form catalyses substrate conversion. 2. GSH inhibits the alkaline phosphatase reversibly and non-competitively by attacking the bound Zn(II). 3. The influenc…

StereochemistrySwineKidneyBiochemistrychemistry.chemical_compoundHydrolysisAnimalsMagnesiumBinding siteMolecular Biologychemistry.chemical_classificationBinding SitesHydrolysisSubstrate (chemistry)Cell BiologyGlutathioneHydrogen-Ion ConcentrationPhosphateAlkaline PhosphataseGlutathioneKineticsZincEnzymechemistryModels ChemicalGlycerophosphatesFunctional groupAlkaline phosphataseResearch ArticleThe Biochemical journal
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Generation, Characterization, and Electrochemical Behavior of the Palladium-Hydride Cluster [Pd3(dppm)3(3-CO)(3-H)]+ (dppm=Bis(diphenylphosphinometha…

2007

Addition of formate on the dicationic cluster [Pd(3)(dppm)(3)(mu(3)-CO)](2+) (dppm=bis(diphenylphosphinomethane) affords quantitatively the hydride cluster [Pd(3)(dppm)(3)(mu(3)-CO)(mu(3)-H)](+). This new palladium-hydride cluster has been characterised by (1)H NMR, (31)P NMR and UV/Vis spectroscopy and MALDI-TOF mass spectrometry. The unambiguous identification of the capping hydride was made from (2)H NMR spectroscopy by using DCO(2) (-) as starting material. The mechanism of the hydride complex formation was investigated by UV/Vis stopped-flow methods. The kinetic data are consistent with a two-step process involving: 1) host-guest interactions between HCO(2) (-) and [Pd(3)(dppm)(3)(mu(3…

Stereochemistrychemistry.chemical_elementPalladium hydride[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryElectrochemistry01 natural sciencesMedicinal chemistryCatalysisReductive eliminationchemistry.chemical_compoundSingle bondComputingMilieux_MISCELLANEOUS010405 organic chemistryHydrideOrganic Chemistryhydrides[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryGeneral Chemistrypalladium0104 chemical sciencesBond lengthchemistryelectrochemistrykineticsProton NMRcluster compoundsPalladium
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Reactivity of dialkoxydibutylstannanes toward carbon dioxide: A DFT study of electronic and steric effects

2012

Abstract DFT calculations were performed for the reaction of CO 2 with the monomeric species, R′ 2 Sn(OR) 2 , (R = R′ = CH 3 ; R = CH 3 , CH 2 CH 3 , CH(CH 3 ) 2 , R′ =  n -Bu) for assessing the role of electronic and steric effects in the kinetics and thermodynamics of CO 2 insertion into Sn–OR bonds. The reaction pathways are exothermic and involve the successive insertion into the two Sn–OR bonds. The driving force for insertion is ascribed to a charge-transfer between the HOMO of the complexes, mainly localized on the oxygen atom of the alkoxy ligands, and the LUMO of CO 2 . Interestingly enough, the energy barrier of the second insertion is much lower by around 27 kJ mol −1 , and quite…

Steric effectsCarbon dioxide fixationKineticsDFT calculation010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistryInorganic Chemistrychemistry.chemical_compound[CHIM.ANAL]Chemical Sciences/Analytical chemistryMaterials ChemistryDialkoxydibutylstannanesReactivity (chemistry)Physical and Theoretical ChemistryHOMO/LUMOAlkylchemistry.chemical_classification010405 organic chemistryLigand0104 chemical sciencesMonomerchemistryAlkoxy group[ CHIM.ANAL ] Chemical Sciences/Analytical chemistryDialkyl carbonatePolyhedron
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Synthesis, characterization and kinetics of the metallation of the intermediate compound to produce compound · (H2O) from Rh(II) tetraacetate

1998

Abstract Photochemical irradiation of mixtures of [Rh2(μ-O2CCH3)4]·(HOCH3)2 and P(2-(CH3O)C6H4)Ph2 (POMe) in CH2Cl2 solution (1:1 molar ratio) yields quantitatively compound [ Rh 2 (μ- O 2 CCH 3 ) 3 ( O 2 CCH 3 )(η 2 - P (2-( CH 3 O ) C 6 H 4 ) Ph 2 ]·( H 2 O ) (1) containing a POMe acting as a chelating equatorial ( P ) axial ( O ) donor ligand. This compound undergoes intramolecular CH activation reaction at one of the phenyl rings in CHCl3 or CH3COOH/toluene solution at room temperature to form the monometallated compound [ Rh 2 (μ- O 2 CCH 3 ) 3 (μ-( C C 3 H 4 ) P (2-( CH 3 O C 6 H 4 ) Ph )]· ( H 2 O ) ( 2 ). The kinetics of the 1 → bd2 reaction have been studied in acid media (CH3CO…

Steric effectsChloroformLigandStereochemistryKineticsMedicinal chemistryTolueneInorganic Chemistrychemistry.chemical_compoundchemistryIntramolecular forceMaterials ChemistryChelationPhysical and Theoretical ChemistryPhosphineInorganica Chimica Acta
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Reactivity of di-tert-butyldimethoxystannane with carbon dioxide and methanol: X-ray structure of the resulting complex

2006

Abstract The synthesis of dimethyl carbonate from carbon dioxide and methanol was studied with ditert-butyldimethoxystannane under pressure at temperatures ⩽423 K. The formation of dimethyl carbonate is accompanied by transformation of the stannane into a trinuclear complex, the structure of which has been determined by single-crystal X-ray diffraction technique. The relevance of this specie in the catalytic cycle is demonstrated by conducting recycling runs. A preliminary kinetic study underlines the steric influence of the tert-butyl ancillary ligands in the stabilisation of intermediates, by comparison with the n-butyl homologue.

Steric effectsInorganic chemistry[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryPhotochemistry01 natural sciencesBiochemistryStannaneCatalysisInorganic Chemistrychemistry.chemical_compounddimethyl carbonateMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSmethanolcatalysis010405 organic chemistryOrganic Chemistrycarbon dioxide[ CHIM.INOR ] Chemical Sciences/Inorganic chemistry0104 chemical sciencesCatalytic cyclechemistrystannanekineticstrinuclearCarbon dioxideMethanolDimethyl carbonateorganotin
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Probing the non-innocent nature of an amino-functionalised β-diketiminate ligand in silylene/iminosilane systems.

2020

Electron-rich β-diketiminate ligands, featuring amino groups at the backbone β positions (“N-nacnac” ligands) have been employed in the synthesis of a range of silylene (SiII) complexes of the type (N-nacnac)SiX (where X = H, Cl, N(SiMe3)2, P(SiMe3)2 and Si(SiMe3)3). A combination of experimental and quantum chemical approaches reveals (i) that in all cases rearrangement to give an aza-butadienyl SiIV imide featuring a contracted five-membered heterocycle is thermodynamically favourable (and experimentally viable); (ii) that the kinetic lability of systems of the type (N-nacnac)SiX varies markedly as a function of X, such that compounds of this type can be isolated under ambient conditions …

Steric effectsMolecular Structure010405 organic chemistryLabilityLigandSilicon CompoundsSilylene010402 general chemistryRing (chemistry)Ligands01 natural sciences3. Good health0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographyKineticschemistryNucleophileIntramolecular forceThermodynamicsIminesImideDensity Functional TheoryDalton transactions (Cambridge, England : 2003)
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