Search results for "Deprotonation"

showing 10 items of 238 documents

From C–S–H to C–A–S–H: Experimental study and thermodynamic modelling

2015

Abstract It has long been known that the stoichiometry of C–S–H varies with the calcium hydroxide concentration in solution. However, this issue is still far from understood. We revisit it in both experimental and modelling aspects. A careful analysis of the solubility confirms the existence of three different C–S–H phases, defined as Ca 4 H 4 Si 5 O 16 , Ca 2 H 2 Si 2 O 7 and Ca 6 (HSi 2 O 7 ) 2 (OH) 2 , respectively. The variation of the Ca/Si ratio of the three phases has been described by surface reactions: the increase of the Si content is accounted for by silicate bridging, the increase of calcium content and the surface charge are accounted for by reactions involving silanol groups v…

AluminateInorganic chemistry0211 other engineering and technologieschemistry.chemical_element02 engineering and technologyBuilding and ConstructionCalcium021001 nanoscience & nanotechnologySilicatechemistry.chemical_compoundSilanolDeprotonationchemistry021105 building & constructionPhysical chemistryGeneral Materials ScienceCalcium silicate hydrateSolubility0210 nano-technologyStoichiometryCement and Concrete Research
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Amino-phosphanes in Rh(I)-catalyzed hydroformylation: new mechanistic insights using D2O as deuterium-labeling agent

2005

International audience; In previous work, we have demonstrated that the dangling amino group in amino-phosphane ligands increases the rate of Rh-catalyzed styrene hydroformylation as a function of the amino group basicity and of the distance between the P and N functions. We now report additional stereochemical and mechanistic insights resulting from new catalytic experiments performed with Rh-α-P,N catalytic systems in the presence of D2O. In addition to the expected D0 product, the formation of the β-D1 aldehyde, PhCH(CH2D)CHO was observed in all cases by 1H and 13C NMR spectroscopy, indicating that H/D exchange occurs for the rhodium-hydride complex. Minor amounts of a β-D2 product, PhCH…

Amino-phosphane ligandsStereochemistryEnantioselectivity010402 general chemistry01 natural sciencesAldehydeInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/CatalysisDeprotonationMoietyRhodium[CHIM.COOR]Chemical Sciences/Coordination chemistryComputingMilieux_MISCELLANEOUSchemistry.chemical_classification010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryHydroformylation catalysis[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[CHIM.CATA]Chemical Sciences/CatalysisAsymmetric induction0104 chemical sciencesEnantiopure drugchemistryH/D isotopic exchangeProtonolysisHydroformylation
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New anionic cobalt complexes using highly hindered bis-amides with varying donor abilities as ligands.

2007

Four potential tetradentate ligands of formulae 1,2-bis-(3,5-di-tert-butyl-2-hydroxybenzamido)ethane (H(4)L(1), 1), 1,2-bis-(3,5-di-tert-butyl-2-hydroxybenzamido)propane (H(4)L(2), 2), 1,2-bis-(3,5-di-tert-butyl-2-hydroxybenzamido)benzene (H(4)L(3), 3) and 1,8-bis-(3,5-di-tert-butyl-2-hydroxybenzamido)naphthalene (H(4)L(4), 4) have been prepared and the crystal structures of three of them (1, 3 and 4) determined by single crystal X-ray diffraction. The investigation of their complexing ability toward Co(II) afforded the compounds of formulae [Co(III)(L(3))Na(I)(H(2)O)(2)] (5), [Co(III)(L(n))Li(I)(H(2)O)2] with n = 1 (6), 2 (7) and 3 (8) and [Co(II)(L(4))Li(I)(2)] (9). Complexes 5-8 are squa…

AnionsMagnetic Resonance SpectroscopyMolecular StructureHydrogen bondStereochemistryLigandSpectrochemical seriesTemperaturechemistry.chemical_elementHydrogen BondingNuclear magnetic resonance spectroscopyCrystal structureCobaltCrystallography X-RayLigandsAmidesInorganic ChemistryCrystallographyMagneticsDeprotonationchemistryOrganometallic CompoundsCobaltSingle crystalDalton transactions (Cambridge, England : 2003)
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Thermodynamic and fluorescence emission studies on chemosensors containing anthracene fluorophores. Crystal structure of {[CuL1Cl]Cl}2·2H2O [L1 = N-(…

1999

The co-ordination capabilities toward hydrogen ions, Co2+, Ni2+, Cu2+, Zn2+ and Cd2+ of the novel receptor 2,6,9,13-tetraaza[14](9,10)anthracenophane (L) and of its open-chain counterpart N-(3-aminopropyl)-N′-3-(anthracen-9-ylmethyl)aminopropylethane-1,2-diamine (L1) is described. Stepwise protonation constants of the cyclic receptor (L) are lower than those of the open-chain receptor (L1) . Quenching effects of the fluorescence emission occur upon first and second deprotonation of L and upon second deprotonation of L1. Stability constants of the Co2+, Ni2+, Cu2+, Zn2+ and Cd2+ complexes follow the Irving–Williams trend and are intermediate between those of triethylenetetraamine with termin…

Anthracenechemistry.chemical_compoundCrystallographyDeprotonationQuenching (fluorescence)chemistrySquare pyramidProtonationGeneral ChemistryCrystal structureTriclinic crystal systemPhotochemistrySquare pyramidal molecular geometry
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Improved Efficacy of Synthesizing *MIII-Labeled DOTA Complexes in Binary Mixtures of Water and Organic Solvents. A Combined Radio- and Physicochemica…

2018

Typically, the synthesis of radiometal-based radiopharmaceuticals is performed in buffered aqueous solutions. We found that the presence of organic solvents like ethanol increased the radiolabeling yields of [68Ga]Ga-DOTA (DOTA = 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacatic acid). In the present study, the effect of organic cosolvents [ethanol (EtOH), isopropyl alcohol, and acetonitrile] on the radiolabeling yields of the macrocyclic chelator DOTA with several trivalent radiometals (gallium-68, scandium-44, and lutetium-177) was systematically investigated. Various binary water (H2O)/organic solvent mixtures allowed the radiolabeling of DOTA at a significantly lower temperature than …

Aqueous solution010405 organic chemistryKineticsProtonation010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundReaction rate constantDeprotonationchemistryDOTAChelationPhysical and Theoretical ChemistryAcetonitrileInorganic Chemistry
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Synthesis, solid state and solution studies of cobalt(II) complexes with 2-hydroxyiminopropanoic acid

2013

Abstract This paper describes the synthesis of the Zn(II) complex with H2L = 2-hydroxyiminopropanoic acid. The final structure incorporated two linear dimeric anions with two Zn2+ atoms, which are linked by a carbonate anion into a tetranuclear unit. In each dinuclear unit, the two Zn(II) ions are coordinated by three molecules of the doubly deprotonated ligand in two different coordination modes. This result is confirmed both by X-ray crystallography and by ESI-MS investigations of the crystals dissolved in water. Equilibrium studies of the zinc(II) complexes formed by H2L in aqueous solution based on independent pH-metric titrations and zinc ion-selective electrode (ISE) titrations indica…

Aqueous solutionChemistryHydrogen bondLigandInorganic chemistrychemistry.chemical_elementProtonationZincInorganic ChemistryCrystallographyDeprotonationMaterials ChemistryMoleculeTitrationPhysical and Theoretical Chemistryta116Polyhedron
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A study of dimethyltin(IV)-L-cysteinate in aqueous solution

1988

The in vivo activity of some R2Sn-L-cysteinate complexes (R = Me, Et, n-Bu) against murine P-388 leukaemia has been tested. Only the Et2Sn(IV) complex showed a marginal positive effect. Trigonal bipyramidal tin environments with two carbon (R) atoms and the sulfur atom in the equatorial plane and oxygen (carboxylate) and nitrogen (NH2) in apical positions have been proposed for the solid compexes (R = Me, Et, n-Bu, Ph) on the basis of experimental Mossbauer parameters and infrared (IR) data. Aqueous solutions of the Me2SnL-cysteinate have been studied by IR, 1H NMR and 119Sn Mossbauer spectroscopy (in frozen solution) at different pH values to identify the Me2Sn(IV) species present. At pH >…

Aqueous solutionChemistryInorganic chemistryInfrared spectroscopychemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyInorganic ChemistryNMR spectra databaseCrystallographychemistry.chemical_compoundTrigonal bipyramidal molecular geometryDeprotonationCarboxylateTinApplied Organometallic Chemistry
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Complex formation of copper( ), nickel( ) and zinc( ) with ethylophosphonoacetohydroxamic acid: solution speciation, synthesis and structural charac…

2019

We present herein the thermodynamic and X-ray characterisation of a novel ethyl phosphonohydroxamic acid-based Cu( ) metallacrown, predominating in solution in a broad pH range.

Aqueous solutionChemistryLigandCoordination polymerIsothermal titration calorimetry02 engineering and technologyGeneral ChemistryCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical sciencesCrystallographychemistry.chemical_compoundDeprotonationMaterials ChemistryChelation0210 nano-technologyMetallacrown
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Synthesis and characterization of acetazolamide complexes of Ni(II), Cd(II), Hg(II), and Ag(I)

1989

The preparation and characterization of K2Ni2(Acm)3·5H2O, Cd(Acm)·32 H2O, Hg(Acm)·12H2O, Ag2(Acm), and Ag2(Acm)(NH3) complexes are described. The spectral properties suggest that Acm interacts with the metal ions through the doubly deprotonated form as observed in the [Cu(Acm)(NH3)2(OH2)]2·2H2O complex, whose crystalline structure has been previously reported. The crystal field parameters of the Ni(II) complex indicate an octahedral environment for the metal ion in the solid and its aqueous, DMSO, and DMF solutions. UV spectra of all the Acm complexes until now synthesized are discussed.

Aqueous solutionChemistryMetal ions in aqueous solutionSpectral propertiesAnalytical chemistryCrystal structureBiochemistryInorganic ChemistryCrystalMetalCrystallographyDeprotonationOctahedronvisual_artvisual_art.visual_art_mediumJournal of Inorganic Biochemistry
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Violurato complexes of nickel(II). Formation equilibria. Deprotonation equilibria of the coordinated ligands and related stereochemical changes

1986

The formation equilibria of nickel(II) violurato-complexes in water and dimethylsulphoxide-water (80∶20) as well as deprotonation of the coordinated ligands and related stereochemical changes are reported. The stability constants of the Ni2+-H2V− complexes logβ1=5.06, Iogβ2=9.38, logβ3=12.98 as well as the acidity constants of the [Ni(H2V)3]− complex, logβj1= 8.37, logβj2=15.76, logβj3=22.37 are determined at 25 °C and 0.1M NaClO4. A new violurato-complex of Ni2+, Na4[Ni(HV)3]5H2O, is isolated and characterized.

Aqueous solutionChemistryStereochemistryOrganic solventMetals and Alloyschemistry.chemical_elementMedicinal chemistryCatalysisInorganic ChemistryNickelchemistry.chemical_compoundDeprotonationStability constants of complexesMaterials ChemistryHydrateOrganometallic chemistryTransition Metal Chemistry
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