Search results for " cations"

showing 10 items of 22 documents

Litter quality, land-use history, and nitrogen deposition effects on topsoil conditions across European temperate deciduous forests

2019

Topsoil conditions in temperate forests are influenced by several soil-forming factors, such as canopy composition (e.g. through litter quality), land-use history, atmospheric deposition, and the parent material. Many studies have evaluated the effects of single factors on physicochemical topsoil conditions, but few have assessed the simultaneous effects of multiple drivers. Here, we evaluate the combined effects of litter quality, land-use history (past land cover as well as past forest management), and atmospheric deposition on several physicochemical topsoil conditions of European temperate deciduous forest soils: bulk density, proportion of exchangeable base cations, carbon/nitrogen-rat…

0106 biological sciencesHigh forestCoppiceManagement Monitoring Policy and LawTemperate deciduous forestSoil fertility010603 evolutionary biology01 natural sciencesNutrient cyclingddc:570Base cationsBosecologie en Bosbeheer/dk/atira/pure/core/keywords/biologyInstitut für Biochemie und BiologieNature and Landscape ConservationEnvironmental planning2. Zero hungerTopsoilDecompositionpHSoil organic matter/dk/atira/pure/core/keywords/557265479Post-agricultural forestForestryPhosphorus15. Life on landPE&RCSoil typeForest Ecology and Forest ManagementAncient forestHigh forestAgronomyEcosystems ResearchSoil waterLitterEnvironmental scienceSoil fertility010606 plant biology & botany
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Sequestration of alkyltin(IV) cations by complexation with amino-polycarboxylic chelating agents

2013

Abstract The binding capacity of four amino-polycarboxylic ligands (APCs) [nitrilotriacetate (NTA), ethylenediamine- N , N , N′ , N′ -tetraacetate (EDTA), (S,S)-ethylenediamine- N , N ′-disuccinic acid (S,S-EDDS) and diethylenetriamine- N , N , N′ , N″ , N″ -pentaacetate (DTPA)] towards mono-, di- and tri-alkyltin(IV) cations [(CH 3 )Sn 3 + , (CH 3 ) 2 Sn 2 + , (C 2 H 5 ) 2 Sn 2 + , (CH 3 ) 3 Sn + or (C 2 H 5 ) 3 Sn + ] was studied, in aqueous solutions, by ISE-H + potentiometry, at I  = 0.1 mol L − 1 (NaCl) and at T  = 298.15 K. In all the systems R x Sn (4 − x)+  − APC (R = CH 3 or C 2 H 5 ) a strong 1:1 species is formed together with protonated, hydroxo and dinuclear complexes. The valu…

Aqueous solutionComplexation in aqueous solutionStereochemistryLigandEthylenediamineProtonationAlkyltin(IV) cations; Amino-polycarboxylic ligands; Complexation in aqueous solution; Sequestration ability of complexones;Condensed Matter PhysicsMedicinal chemistryAtomic and Molecular Physics and OpticsAlkyltin(IV) cationElectronic Optical and Magnetic MaterialsIonAmino-polycarboxylic ligandchemistry.chemical_compoundSequestration ability of complexoneschemistryDiethylenetriamineMaterials ChemistryChelationSettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistrySimple correlationSpectroscopy
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Electronic aspects of the hydride transfer mechanism. Ab initio analytical gradient studies of the cyclopropenyl‐cation/lithium hydride model reactan…

1985

The electronic mechanisms of a model hydride transfer reaction are theoretically studied with ab inito RHF and UHF SCF MO procedures at the 4‐31G basis set level and analytical gradient methods. The model system describes the reduction of cyclopropenyl cation to cyclopropene by the oxidation of lithium hydride to lithium cation. The molecular fragments corresponding to the asymptotic reactive channels characterizing the stepwise mechanisms currently discussed in the literature have been characterized. The binding energy between the fragments is estimated within a simple electrostatic approximate scheme. The results show that a hydride‐ion mechanism is a likely pathway for this particular sy…

Biological MaterialsAb initioGeneral Physics and Astronomychemistry.chemical_elementchemistry.chemical_compoundElectron transferAb initio quantum chemistry methodsComputational chemistry:FÍSICA [UNESCO]CationsRedox ProcessPhysical and Theoretical ChemistryTriplet stateCycloalkenes:FÍSICA::Química física [UNESCO]HydrideUNESCO::FÍSICAChemical ReactionsUNESCO::FÍSICA::Química físicachemistryLithium hydrideChemical physicsLithium HydridesAb Initio Calculations ; Chemical Reactions ; Cycloalkenes ; Cations ; Lithium Hydrides ; Redox Process ; Biological MaterialsLithiumLithium CationAb Initio Calculations
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Calculation of size‐intensive transition moments from the coupled cluster singles and doubles linear response function

1994

Coupled cluster singles and doubles linear response (CCLR) calculations have been carried out for excitation energies and dipole transition strengths for the lowest excitations in LiH, CH+, and C4and the results compared with the results from a CI-like approach to equation of motion coupled cluster (EOMCC). The transition strengths are similar in the two approaches for single molecule calculations on small systems. However, the CCLR approach gives size-intensive dipole transition strengths, while title EOMCC formalism does not. Thus, EOMCC calculations can give unphysically dipole transition strengths, e.g., in EOMCC calculations on a sequence of noninteracting LiH systems we obtained a neg…

DipolesGeneral Physics and AstronomySmall systemsExcitation ; Dipoles ; Lithium Hydrides ; Carbynes ; Cations ; Molecular Ions ; Carbon Molecules ; Equations Of Motion ; Correlations ; Response FunctionsPhysics and Astronomy (all)CationsMoleculePhysical and Theoretical Chemistry:FÍSICA::Química física [UNESCO]ExcitationCorrelationsChemistryEquations of motionCarbon MoleculesLinear response functionUNESCO::FÍSICA::Química físicaFormalism (philosophy of mathematics)DipoleCoupled clusterLithium HydridesCarbynesResponse FunctionsAtomic physicsEquations Of MotionMolecular IonsExcitationThe Journal of Chemical Physics
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Structure of matrices based on pectin : formulation, characterization, functionality and controlled release during the encapsulation

2016

In this thesis, we studied the interactions between an anionic polysaccharide (pectin) and monovalent cation (Na+) and divalent cations (Ca2+, Zn2+, Ba2+, Mg2+) in dilute regime (c Ca2+ > Zn2+ > Mg2+; this may be related to the affinity between the water molecules from the coordination sphere and the cation. Indeed, the affinity of the cation for water molecules increases in the reverse order: Ba2+ < Ca2+ < Zn2+ < Mg2+. Finally, we have used the three polysaccharides (PGA, LMP and ALMP - amidated low methoxyl pectin) in association with calcium ions to produce microparticles containing rutin to target drug release in the intestine. We have linked the rutin release kinetics to the network st…

Divalent cationsGelNaClMécanisme d’associationBinding mechanismCations divalentsPectinsStructureEncapsulationPectines[SDV.IDA] Life Sciences [q-bio]/Food engineering[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]
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Understanding the Solution Behavior of Epinephrine in the Presence of Toxic Cations: A Thermodynamic Investigation in Different Experimental Conditio…

2020

The interactions of epinephrine ((R)-(&minus

EnthalpyInorganic chemistryPharmaceutical ScienceIonic bondingProtonation02 engineering and technologyCalorimetry010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug Discoverytoxic cationSettore CHIM/01 - Chimica Analiticatoxic cationsepinephrinePhysical and Theoretical ChemistryChemistryOrganic Chemistryenthalpy and entropy changesOxidesMethylmercury Compoundsdependence on ionic strength021001 nanoscience & nanotechnologysequestering ability0104 chemical sciencesSpecific ion interaction theoryChemistry (miscellaneous)Ionic strengthBenzyl alcoholThermodynamicsUraniumMolecular MedicineTitration0210 nano-technologyenthalpy and entropy changeMolecules
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Tetraalkylammonium Cations Conduction through a Single Nanofluidic Diode: Experimental and Theoretical Studies

2017

[EN] We describe experimentally and theoretically the concentration-dependent conduction of tetraalkylammonium (TAA+) cations through a nanofluidic diode fabricated in a polymer membrane via asymmetric track-etching techniques. This single-pore membrane exhibits current rectification characteristics because of the ionized carboxylate groups on the pore surface. We use aqueous solutions of potassium (K+ ), ammonium (A+ ), tetramethylammonium (TMA+ ), tetraethylammonium (TEA+ ), and tetrabutylammonium (TBA+ ) ions with concentrations ranging from 50 to 500 mM under acidic (pH 3.5) and physiological (pH 6.5) conditions. Compared with the K+ and A+ ions, the TMA+ , TEA+ , and TBA+ ions show rel…

General Chemical EngineeringInorganic chemistryAnalytical chemistry02 engineering and technology010402 general chemistry01 natural sciencesIonchemistry.chemical_compoundAdsorptionElectrochemistryNernst-Planck equationCarboxylateSurface chargeAlkylTetraalkyammonium cationsTetramethylammoniumchemistry.chemical_classificationAqueous solutionBiomimetic nanoporeCurrent rectification021001 nanoscience & nanotechnology0104 chemical sciencesMembraneNanofluidic diodechemistryFISICA APLICADA0210 nano-technology
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COVID-19, Cation Dysmetabolism, Sialic Acid, CD147, ACE2, Viroporins, Hepcidin and Ferroptosis: A Possible Unifying Hypothesis.

2022

Background: iron and calcium dysmetabolism, with hyperferritinemia, hypoferremia, hypocalcemia and anemia have been documented in the majority of COVID-19 patients at later/worse stages. Furthermore, complementary to ACE2, both sialic acid (SA) molecules and CD147 proved relevant host receptors for SARS-CoV-2 entry, which explains the viral attack to multiple types of cells, including erythrocytes, endothelium and neural tissue. Several authors advocated that cell ferroptosis may be the core and final cell degenerative mechanism. Methods: a literature research was performed in several scientific search engines, such as PubMed Central, Cochrane Library, Chemical Abstract Service. More than 5…

General Immunology and MicrobiologySARS-CoV-2virusesvirus diseasesCOVID-19Endothelial CellsGeneral Medicinebiochemical phenomena metabolism and nutritionGeneral Biochemistry Genetics and Molecular BiologyN-Acetylneuraminic AcidViroporin ProteinsHepcidinsCationsferroptosis cations sialic acid iron ferritin calcium viroporins voltage-gated calcium channels cell membrane CD147 ACE2 hepcidin red blood cells hemoglobin mitochondriaFerroptosisHumansAngiotensin-Converting Enzyme 2General Pharmacology Toxicology and PharmaceuticsF1000Research
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The use of tree-rings and foliage as an archive of volcanogenic cation deposition.

2007

Tree cores (Pinus nigra ssp. laricio) and leaves (Castanea sativa) from the flanks of Mount Etna, Sicily were analysed by ICP-MS to investigate whether volcanogenic cations within plant material provide an archive of a volcano's temporal and spatial depositional influence. There is significant compositional variability both within and between trees, but no systematic dendrochemical correlation with periods of effusive, explosive or increased degassing activity. Dendrochemistry does not provide a record of persistent but fluctuating volcanic activity. Foliar levels of bioaccumulated cations correspond to modelled plume transport patterns, and map short-term volcanic fumigation. Around the fl…

Health Toxicology and MutagenesisMineralogychemistry.chemical_elementAcerVolcanismVolcanic EruptionsToxicologyHistory 21st CenturyTreesSedimentary depositional environmentCationsMount Etna Volcanogenic cations Tree-rings Pinus nigra Castanea sativaTiliaVolatilesSicilygeographyStrontiumAir Pollutantsgeography.geographical_feature_categorybiologyHistory 19th CenturyGeneral MedicineHistory 20th Centurybiology.organism_classificationPinusPollutionPlumePlant LeavesDeposition (aerosol physics)VolcanochemistryPinaceaeGeologyEnvironmental MonitoringEnvironmental pollution (Barking, Essex : 1987)
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Effect of the Alkaline Cations on the Stability of the Model Polynucleotide Poly(dG-dC)·Poly(dG-dC)

2011

When the model polynucleotide poly(dG-dC)∙poly(dG-dC) [polyGC] is titrated with a strong acid (HCl) in unbuffered aqueous solutions containing the chlorides of the alkali metals in the concentration range 0.010 M-0.600 M, two transitions in the absorbance vs. pH plots are evidenced, characterized by the constants pK(a(₁)) and pK(a(₂)). The limiting values at infinite saline concentrations of these two constants, namely pK(∞)(a(₁)) and pK(∞)(a(₂)) obtained making use of the "one site saturation constant" equation or, in turn, of the double logarithmic plot: pK(a) vs. log([salt]⁻¹), exhibit a clear dependence on the nature of the cations. The effects of the different alkali cations on the pK(…

Hofmeister seriesalkaline cationsSodiumPolynucleotidesInorganic chemistryAnalytical chemistrychemistry.chemical_elementSodium Chloridemodel polynucleotidesAbsorbancePolydeoxyribonucleotidesUltraviolet visible spectroscopyalkaline cations; hofmeister effect; model polynucleotides; uv-spectroscopyStructural BiologyCationsuv-spectroscopyhofmeister effectMicroemulsionAlkaline cationMolecular BiologyAqueous solutionMetals AlkaliChemistryModel polynucleotideGeneral MedicineHydrogen-Ion ConcentrationAlkali metalPolynucleotideNucleic Acid ConformationJournal of Biomolecular Structure and Dynamics
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