Search results for "Chemical stability"

showing 10 items of 96 documents

A solution study of complex formation between iron(III) and oxalate in dimethylsulphoxide

1991

The complex formation between iron(III) and oxalic acid (ethanedioic acid, H2ox) has been studied by potentiometry in dimethylsulphoxide (dmso) solution. H2ox behaves as a weak diprotic acid in such a solvent, with overall association constants: log βj1=8.551(3) and log βj2=14.242(3) at 25°C and 0.1 Mn-Bu4NClO4. A reliable set of overall stability constants for the iron(III)-oxalato complexes, log β11=13.16(4), log β12=23.66(4) and log β13=30.75(4), have been obtained for the first time under identical conditions. The electrochemical behaviour of such complexes was studied in dmso at a platinum electrode. The coordination ability of oxalate towards iron(III) in dmso and water media is compa…

Oxalic acidInorganic chemistryMetals and Alloyschemistry.chemical_elementDiprotic acidOxalateInorganic ChemistrySolventchemistry.chemical_compoundchemistryMaterials ChemistryChemical stabilityCarboxylateCyclic voltammetryPlatinumTransition Metal Chemistry
researchProduct

De novo synthesis of mesoporous photoactive titanium(IV)-organic frameworks with MIL-100 topology

2019

[EN] Most developments in the chemistry and applications of metal-organic frameworks (MOFs) have been made possible thanks to the value of reticular chemistry in guiding the unlimited combination of organic connectors and secondary building units (SBUs) into targeted architectures. However, the development of new titanium-frameworks still remains limited by the difficulties in controlling the formation of persistent Ti-SBUs with predetermined directionality amenable to the isoreticular approach. Here we report the synthesis of a mesoporous Ti-MOF displaying a MIL-100 topology. MIL-100(Ti) combines excellent chemical stability and mesoporosity, intrinsic to this archetypical family of porous…

Materials science010405 organic chemistryQuímica organometàl·licachemistry.chemical_elementGeneral ChemistryMicroporous material010402 general chemistryTopology01 natural sciences0104 chemical sciencesQUIMICA ORGANICAchemistryChemical stabilitySBusMesoporous materialPorous mediumPorosityTopology (chemistry)Titanium
researchProduct

The tetrameric α-helical membrane protein GlpF unfolds via a dimeric folding intermediate.

2011

Many membrane proteins appear to be present and functional in higher-order oligomeric states. While few studies have analyzed the thermodynamic stability of α-helical transmembrane (TM) proteins under equilibrium conditions in the past, oligomerization of larger polytopic monomers has essentially not yet been studied. However, it is vital to study the folding of oligomeric membrane proteins to improve our understanding of the general mechanisms and pathways of TM protein folding. To investigate the folding and stability of the aquaglyceroporin GlpF from Escherichia coli, unfolding of the protein in mixed micelles was monitored by steady-state fluorescence and circular dichroism spectroscopy…

Gel electrophoresisCircular dichroismProtein FoldingChemistryCircular DichroismEscherichia coli ProteinsMembrane ProteinsAquaporinsBiochemistryMicelleTransmembrane proteinProtein Structure SecondaryFolding (chemistry)CrystallographyKineticsMembrane proteinBiophysicsEscherichia coliProtein foldingChemical stabilityDimerizationProtein UnfoldingBiochemistry
researchProduct

Design of stable mixed-metal MIL-101(Cr/Fe) materials with enhanced catalytic activity for the Prins reaction

2020

[EN] This work highlights the benefit of designing mixed-metal (Cr/Fe) MOFs for enhanced chemical stability and catalytic activity. A robust and stable mixed-metal MIL-101(Cr/Fe) was prepared through a HF-free direct hydrothermal route with Fe(3+)content up to 21 wt%. The incorporation of Fe(3+)cations in the crystal structure was confirmed by(57)Fe Mossbauer spectrometry. The catalytic performance of the mixed metal MIL-101(Cr/Fe) was evaluated in the Prins reaction. MIL-101(Cr/Fe) exhibited a higher catalytic activity compared to MIL-101(Cr), improved chemical stability compared to MIL-101(Fe) and a higher catalytic activity for bulky substrates compared to MIL-100(Fe).In situinfra-red sp…

Crystal structure010402 general chemistry01 natural sciencesHydrothermal circulationIonCatalysisQUIMICA ORGANICAQUIMICA ANALITICA[CHIM]Chemical SciencesGeneral Materials ScienceLewis acids and bases[PHYS.COND]Physics [physics]/Condensed Matter [cond-mat]MaterialsComputingMilieux_MISCELLANEOUSMossbauer spectrometry[PHYS]Physics [physics]010405 organic chemistryRenewable Energy Sustainability and the EnvironmentChemistryGeneral ChemistryPrins reaction0104 chemical sciencesChemical stabilityQuímica orgànicaNuclear chemistryJournal of Materials Chemistry A
researchProduct

The role of water in hemoglobin function and stability

1993

MultidisciplinaryChemistryAllosteric regulationThermodynamicsChemical stabilityHemoglobinStability (probability)Function (biology)
researchProduct

Stability of biogenic metal(loid) nanomaterials related to the colloidal stabilization theory of chemical nanostructures

2018

In the last 15 years, the exploitation of biological systems (i.e. plants, bacteria, mycelial fungi, yeasts, and algae) to produce metal(loid) (Me)-based nanomaterials has been evaluated as eco-friendly and a cost-effective alternative to the chemical synthesis processes. Although the biological mechanisms of biogenic Me-nanomaterial (Bio-Me-nanomaterials) production are not yet completely elucidated, a key advantage of such bio-nanostructures over those chemically synthesized is related to their natural thermodynamic stability, with several studies ascribed to the presence of an organic layer surrounding these Bio-Me-nanostructures. Different macromolecules (e.g. proteins, peptides, lipids…

Metalloid02 engineering and technology010402 general chemistryPolysaccharide01 natural sciencesApplied Microbiology and BiotechnologyChemical synthesisNanomaterialsstericOrganic chemistryColloidsBiological metal nanomaterialcolloidal stabilityDLVO theoryMetalloidschemistry.chemical_classificationbiologyMetalChemistryGeneral Medicine021001 nanoscience & nanotechnologybiology.organism_classificationTerpenoidNanostructures0104 chemical sciencesMetalselectrosteric interactionColloidChemical stabilityMetalloid0210 nano-technologyelectrostaticBacteriaBiotechnologyMacromoleculeCritical Reviews in Biotechnology
researchProduct

Geminal Imidazolium Salts: A new Class of Gelators

2012

The gelling behavior of some geminal diimidazolium salts was investigated in solvents differing in polarity and hydrogen bond donor ability. The used salts, namely the 3,3'-di-n-decyl-1,1'(1,4-phenylenedimethylene)diimidazolium dibromide [p-Xyl-(decim)(2)][Br](2) (1), the 3,3'-di-n-dodecyl-1,1'(1,4-phenylenedimethylene)diimidazolium dibromide [p-Xyl-(dodecim)(2)][Br](2) (2), and the 3,3'-di-n-dodecyl-1,1'(1,4-phenylenedimethylene)diimidazolium ditetrafluoroborate [p-Xyl-(dodecim)(2)][BF(4)](2) (3), differ in the alkyl chain length and in the anion properties, such as size, shape, and coordination ability. In all cases in which gelation process was observed, the obtained gels were characteri…

Supramolecular chemistrychemistry.chemical_compoundBromidePolymer chemistryElectrochemistryMoleculeOrganic chemistryGeneral Materials ScienceSpectroscopyAlkylchemistry.chemical_classificationMolecular StructureGeminalHydrogen bondChemistryImidazolesHydrogen BondingSurfaces and InterfacesSettore CHIM/06 - Chimica OrganicaCondensed Matter PhysicsResonance (chemistry)Geminal imidazolium salts Low molecular weight gelator OrganogelThermodynamicsSaltsChemical stabilityGelsOrganogels Hydrogels imidazolium salts
researchProduct

A phosphonamidate containing aromatic N-terminal amino group as inhibitor of leucine aminopeptidase-design, synthesis and stability.

2006

Fully deprotected phosphonamidate dipeptides, predicted as effective inhibitors of cytosolic leucine aminopeptidase, showed unexpected instability in water solution at pH below 12. Their hydrolysis rate was strictly correlated with basicity of the N-terminal amino group. To improve this feature a phosphonamidate analogue containing less basic, aromatic 2-aminophenylphosphonate residue in P1 position of the inhibitor was designed. The target compound was synthesised starting from diethyl 2-nitrophosphonate in several step procedure. The decrease in basicity of the terminal amino moiety of the modified analogue in fact resulted in satisfactory improvement of hydrolytic stability of the P–N bo…

PharmacologyModels MolecularMagnetic Resonance SpectroscopyChemistryStereochemistryphosphonamidateLAP inhibitorsOrganic ChemistryGeneral MedicineAminopeptidaseChemical synthesisResidue (chemistry)HydrolysisLeucyl AminopeptidaseOrganophosphorus CompoundsDrug StabilityDrug DesignDrug Discoveryhydrolytic stabilityMoietyChemical stabilityProtease InhibitorsLeucineLeucyl aminopeptidaseEuropean journal of medicinal chemistry
researchProduct

Two-Component Hydrogels Formed by Cyclodextrins and Dicationic Imidazolium Salts

2013

In the framework of our recent interest in studying the gelling behaviour of imidazolium salts, we took into account the possibility of obtaining two-component hydrogels by combining cyclodextrins and dicationic imidazolium salts. In particular, we used diimidazolium salts differing in the alkyl chain length and in the size, shape, and coordination ability of the anion, namely the 3,3′-di-n-decyl- and 3,3′-di-n-dodecyl-1,1′-(1,4-phenylenedimethylene)diimidazolium dibromide, and 3,3′-di-n-dodecyl-1,1′-(1,4-phenylenedimethylene)diimidazolium ditetrafluoroborate and dihexafluorophosphate. As far as cyclodextrins are concerned, to gain information on the effects of different sized cyclic oligos…

chemistry.chemical_classificationCyclodextrinOrganic ChemistryResonance (chemistry)FluorescencechemistryChemical engineeringSelf-healing hydrogelsProton NMROrganic chemistryChemical stabilityPhysical and Theoretical ChemistrySpectroscopyAlkylEuropean Journal of Organic Chemistry
researchProduct

Dehydration of detomidine hydrochloride monohydrate

2010

The thermodynamic stability of detomidine hydrochloride monohydrate has been evaluated on the basis of phase transition kinetics in solid state. A method free of empirical models was used for the treatment of kinetic data, and compared to several known solid state kinetic data processing methods. Phase transitions were monitored by powder X-ray diffraction (PXRD) and thermal analysis. Full PXRD profiles were used for determining the phase content instead of single reflex intensity measurements, in order to minimize the influence of particle texture. We compared the applicability of isothermal and nonisothermal methods to our investigation of detomidine hydrochlorine monohydrate dehydration.

Phase transitionDetomidineDifferential Thermal AnalysisChemistryImidazolesAnalytical chemistryPharmaceutical SciencePhase TransitionIsothermal processKineticsDrug StabilityModels ChemicalX-Ray DiffractionDifferential thermal analysisPhase (matter)Adrenergic alpha-2 Receptor AgonistsmedicineThermodynamicsChemical stabilityDesiccationThermal analysisPowder DiffractionPowder diffractionmedicine.drugEuropean Journal of Pharmaceutical Sciences
researchProduct