Search results for "equilibrium constant"

showing 9 items of 79 documents

The Born–Oppenheimer equilibrium bond distance of GeO from millimetre- and submillimetre-wave spectra and quantum-chemical calculations

2014

The millimetre- and submillimetre-wave spectra of the five common isotopologues of (GeO)-O-16 in their electronic and vibrational ground state have been recorded in the spectral region 115-732GHz; for (GeO)-Ge-74-O-16, the rotational spectrum in the v = 1 state has been detected as well. Exploiting the high precision of the measurements, the Born-Oppenheimer breakdown parameter Delta(Ge)(01) could be determined from a Dunham analysis of the spectral data, whereas Delta(O)(01) was obtained from quantum-chemical calculations, because of the lack of high-precision measurements for the (GeO)-O-18 isotopologues. From the rotational equilibrium constant, the Born-Oppenheimer equilibrium distance …

equilibrium bond distanceBorn-Oppenheimer breakdownrotational spectrumChemistryBiophysicsBorn–Oppenheimer approximationCondensed Matter PhysicsSpectral linequantum-chemical calculationBond lengthsymbols.namesakeRotational spectrumsymbolsMillimeterIsotopologuePhysical and Theoretical ChemistryAtomic physicsGround stateMolecular BiologyAstrophysics::Galaxy AstrophysicsEquilibrium constant
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Tuning the Electrochemistry of Free-Base Porphyrins in Acidic Nonaqueous Media: Influence of Solvent, Supporting Electrolyte, and Ring Substituents

2016

International audience; A detailed study of reduction potentials, electroreduction mechanisms and acid-base chemistry was carried out on two series of free-base porphyrins in nonaqueous media. The first series is represented by four-pyrrole substituted tetraphenylporphyrin (TPP) derivatives, two of which are planar and two of which are nonplanar in their non-protonated form. The second comprises porphyrins with 0-4 meso-phenyl groups on the macrocycle. Equilibrium constants for conversion of each neutral porphyrin to its diprotic [H4P] 2+ form were determined and the electrochemistry was then elucidated as a function of: (i) type of nonaqueous solvent, (ii) anion of supporting electrolyte, …

free-base porphyrinsSupporting electrolyteprotonationInorganic chemistry010402 general chemistryElectrochemistry[ CHIM ] Chemical Sciences01 natural sciencesCatalysistetraphenylporphyrin monoacidschemistry.chemical_compoundconformational-analysismetal derivativesTetraphenylporphyrin[CHIM]Chemical SciencesReactivity (chemistry)tetraarylporphyrinsEquilibrium constantcomplexes010405 organic chemistryFree basecrystal-structurespectroelectrochemistryanionDiprotic acidPorphyrin0104 chemical sciencessupporting electrolytechemistryelectrochemistryexpanded porphyrindiacids[CHIM.OTHE]Chemical Sciences/Otherabsorption
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Electronic and Steric Effects: How Do They Work in Ionic Liquids? The Case of Benzoic Acid Dissociation

2010

The need to have a measure of the strength of some substituted benzoic acids in ionic liquid solution led us to use the protonation equilibrium of sodium p-nitrophenolate as a probe reaction, which was studied by means of spectrophotometric titration at 298 K. In order to evaluate the importance of electronic effect of the substituents present on the aromatic ring, both electron-withdrawing and -donor substituents were taken into account. Furthermore, to have a measure of the importance of the steric effect of the substituents both para- and ortho-substituted benzoic acids were analyzed. The probe reaction was studied in two ionic liquids differing for the ability of the cation to give hydr…

inorganic chemicalsSteric effectsionic liquids ion pair formation carboxylic acidsChemistryHydrogen bondorganic chemicalsOrganic ChemistryInorganic chemistryProtonationSettore CHIM/06 - Chimica OrganicaDissociation (chemistry)chemistry.chemical_compoundIonic liquidElectronic effectEquilibrium constantBenzoic acidThe Journal of Organic Chemistry
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Determination of the atmospheric precipitation pH value on the basis of the analysis of lichen cationoactive layer constitution

2006

Studies of equilibria and kinetics of the ion exchange process between the surrounding (water solution) and lichens prove that the number of mobile hydrogen ions bonded in lichens depends on the concentration of hydrogen ions in the precipitation with which the lichens are in contact and the type and concentration of other cations contained in the precipitation. The measurement of these values was suggested; as a result, it enabled to determine the pH of precipitation by determination of mobile cations bonded in exposed or naturally grown lichens. The studies were conducted on Hypogymnia physodes lichens.

integumentary systemIon exchangeHydrogenPrecipitation (chemistry)ChemistryGeneral Chemical EngineeringKineticschemistry.chemical_elementIonstomatognathic diseasesstomatognathic systemEnvironmental chemistryElectrochemistryAcid rainskin and connective tissue diseasesLichenEquilibrium constantElectrochimica Acta
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Propuesta de un test para determinar el conocimiento conceptual de estudiantes universitarios sobre la constante de equilibrio químico y su aplicació…

2014

This article outlines a procedure that was used to develop a written test for evaluating the conceptual knowledge of chemical equilibrium constant among university students. The concepts in the subject matter were carefully defined through propositional statements. Students" understanding of the topic was determined through interviews. These data were used to produce nine multiple choice questions. Each question was designed to identify misconceptions related to the chemical equilibrium constant. The test was evaluated by foure associate professors and was administred to a total of 196 spanish university students. This test has a Cronbach"s alpha reliability of 0.63 and its content validity…

lcsh:ChemistryEducació Avaluaciótestlcsh:QD1-999educationconceptual knowledgechemical equilibrium constantEnsenyament universitariQuímicaQuímica Nova
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Definición y unidades de las constantes de equilibrio en los libros de texto de Química general preuniversitarios y universitarios

2021

En este trabajo, una vez definidas las constantes de equilibrio experimentales, Kp y Kc, así como la constante de equilibrio termodinámica, Kº, se analiza su incorrecto tratamiento por parte de libros de texto de química general. Se expone la forma en que libros de química general de universidad y de bachillerato manejan las unidades de las constantes de equilibrio. Muchos textos no expresan con unidades los valores de Kp y Kc calculados. Además, en la mayoría de los casos, Kº no se define, y como resultado existe una confusión muy extendida acerca de estos conceptos. Este problema terminológico ocasiona que en muchos libros se confunda Kp con Kº. Se propone que la definición correcta de la…

químicainvestigación sobre literatura científicaTermodinámicaTextbook analysisanálisis de contenidoAnàlisi de textosQuímica generalestudios científicosEducationEquilibrium constantsAnálisis de textoseducación científicaConstantes de equilibrioGeneral chemistryTermodinàmicaThermodynamicslibro de textoConstants d'equilibriterminología
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A Theoretical and Experimental Investigation of the Spectroscopic Properties of a DNA-Intercalator Salphen-Type ZnIIComplex

2014

The photophysical and DNA-binding properties of the cationic zinc(II) complex of 5-triethylammonium methyl salicylidene ortho-phenylenediiminato (ZnL 2 + ) were investi- gated by a combination of experimental and theoretical methods. DFT calculations were performed on both the ground and the first excited states of ZnL 2 + and on its possi- ble mono- and dioxidation products, both in vacuo and in selected solvents mimicked by the polarizable continuum model. Comparison of the calculated absorption and fluores- cence transitions with the corresponding experimental data led to the conclusion that visible light induces a two-elec- tron photooxidation process located on the phenylenediimi- nato…

spectroscopyNO ligandStereochemistryIntercalation (chemistry)Ionic bondingmetal complex Fluorescence spectroscopy DNA recognition metal complexes organometallics complex formation DNA binding drugs fluorescence spectroscopy equilibrium constants reaction mechanisms nucleic acids affinity binding mode thermodynamics speciationmetal complexesbinding modePhenylenediaminesPolarizable continuum modelCatalysisdrugsmetal complexthermodynamicsintercalationcomplex formationOrganometallic CompoundsA-DNADNA bindingFluorescence spectroscopyDNA recognitionphotochemistryLigandChemistrySpectrum AnalysisphotooxidationOrganic ChemistryCationic polymerizationequilibrium constantsGeneral Chemistrydensity functional calculationFluorescenceZincCrystallographyreaction mechanismsnucleic acidsspeciationSettore CHIM/03 - Chimica Generale E InorganicaExcited stateaffinityfluorescenceorganometallics
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DEVELOPMENT OF A TEST FOR EVALUATING THE CONCEPTUAL KNOWLEDGE OF CHEMICAL EQUILIBRIUM CONSTANT AMONG UNIVERSITY STUDENTS AND ITS APPLICATION TO SPANI…

2014

This article outlines a procedure that was used to develop a written test for evaluating the conceptual knowledge of chemical equilibrium constant among university students. The concepts in the subject matter were carefully defined through propositional statements. Students' understanding of the topic was determined through interviews. These data were used to produce nine multiple choice questions. Each question was designed to identify misconceptions related to the chemical equilibrium constant. The test was evaluated by foure associate professors and was administred to a total of 196 spanish university students. This test has a Cronbach's alpha reliability of 0.63 and its content validity…

testCronbach's alphaconceptual knowledgechemical equilibrium constanteducationContent validityGeneral ChemistryPsychologyHumanitiesSubject matterTest (assessment)Multiple choiceQuímica Nova
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Volumes of aqueous block copolymers based on poly(propylene oxides) and poly(ethylene oxides) in a large temperature range: A quantitative description

2006

The focus of this paper was on a quantitative comprehension of temperature effect on the volumes of aqueous di-block and triblock copolymers, based on propylene oxide (PO) and ethylene oxide (EO) units. To this purpose, literature data dealing with (EO316PO94 + water) and (EO13PO30EO13 + water) mixtures were analyzed. The volume vs. temperature trends were rationalized on the basis of the (unimers + aggregate) equilibrium by taking into account the temperature effect on both the partial molar volumes of the unimeric and the aggregated copolymer as well as the equilibrium constant of micellization. The analysis extended to the expansibility allowed to quantify the contribution for the shift …

volumecopolymerAqueous solutionEthylene oxideaggregationAnalytical chemistryFraction (chemistry)expansibilityAtmospheric temperature rangeAtomic and Molecular Physics and Opticsmodellingchemistry.chemical_compoundVolume (thermodynamics)chemistryPolymer chemistryCopolymerGeneral Materials SciencePropylene oxidePhysical and Theoretical ChemistryEquilibrium constantThe Journal of Chemical Thermodynamics
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