Search results for "DEP"

showing 10 items of 10555 documents

Bis(oxamato)palladate(II) complexes: synthesis, crystal structure and application to catalytic Suzuki reaction

2015

New bis(oxamato)palladate(II) complexes, [Pd(H2O)4][Pd(2,6-Me2pma)2]·2H2O (1), (n-Bu4N)2[Pd(2,6-Me2pma)2]·2H2O (2a), and (n-Bu4N)2[Pd(2,6-Me2pma)2]·2CHCl3 (2b) (2,6-Me2pma = N-2,6-dimethylphenyoxamate and n-Bu4N+ = tetra-n-butylammonium), have been synthesized and the structures of 1 and 2b characterized by single-crystal X-ray diffraction. Complex 1 is a double salt constituted by tetraaquapalladium(II) cations and bis(oxamato)palladate(II) anions interlinked by hydrogen bonds. The palladium(II) ions in 1 are four-coordinate with two oxygens and two nitrogens from two fully deprotonated oxamate ligands (anion), and four water molecules (cation) building centrosymmetric square-planar surrou…

chemistry.chemical_classificationChemistryStereochemistryArylIodidechemistry.chemical_elementCrystal structureMedicinal chemistrychemistry.chemical_compoundDouble saltDeprotonationSuzuki reactionBromideMaterials ChemistryPhysical and Theoretical ChemistryPalladium
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ChemInform Abstract: Enantioselective Synthesis of α-Quaternary Amino Acids by Alkylation of Deprotonated α-Aminonitriles.

2015

An α-alkylation of deprotonated α-amino nitriles, prepared from chiral phenyldioxanamine (I) by Strecker reaction, leads to α-quaternary arylglycines with high optical purity after hydrolysis and oxidative cleavage of the chiral auxiliary.

chemistry.chemical_classificationChiral auxiliarychemistry.chemical_compoundHydrolysisDeprotonationchemistryStrecker amino acid synthesisEnantioselective synthesisGeneral MedicineAlkylationEnantiomeric excessMedicinal chemistryAmino acidChemInform
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An On/Off Circular Dichroism Signal Reveals a pH Dependent Competition between a Cyclodextrin and a Polyelectrolyte for an Atropisomeric Aromatic Gue…

1997

chemistry.chemical_classificationCircular dichroismCyclodextrinChemistrymedia_common.quotation_subjectPh dependentGeneral ChemistryPhotochemistryBiochemistrySignalCatalysisCompetition (biology)PolyelectrolyteColloid and Surface ChemistryOrganic chemistrymedia_commonJournal of the American Chemical Society
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Optical tweezing electrophoresis of isolated, highly charged colloidal spheres

2001

Abstract We report on a novel optical tweezing experiment measuring the electrophoretic mobility μ of highly charged spherical particles suspended in water at volume fractions Φ≤2×10 −7 . At deionised conditions μ =2.5×10 −8 m 2 V −1 s −1 , it decreases further upon increasing the salt concentration c . We compare our data to measurements at larger Φ, where generally much larger μ and a qualitatively different dependence on the salt concentration are observed. To characterise the dependence on Φ we performed measurements at no added salt. There the mobility increases in the unordered state but stays constant at μ =6.8×10 −8 m 2 V −1 s −1 as the system develops fluid order. In the ordered re…

chemistry.chemical_classificationColloidElectrokinetic phenomenaElectrophoresisColloid and Surface ChemistryConcentration dependencechemistryVolume (thermodynamics)Analytical chemistrySalt (chemistry)SPHERESColloids and Surfaces A: Physicochemical and Engineering Aspects
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Atomic force microscopy study of conducting polymer films near electrode's edge or grown on microband electrode

2013

Abstract Polypyrrole (PPy) films of different thicknesses (within the range from 200 nm to 2.5 μm) were electrodeposited on two types of inhomogeneous substrates, single band and double-band Pt electrodes. Topographic images of the polymer layers were obtained by means of ex situ large-scale AFM technique to demonstrate how the propagation rates of the film growth above the electrode (in the normal direction to the electrode surface) and along the insulating surface surrounding the single- or double-band electrodes (in the horizontal direction) change with the deposition charge. It is proved that variations in the film thickness over the double band electrodes and progressive changes of the…

chemistry.chemical_classificationConductive polymerMaterials scienceGeneral Chemical EngineeringAnalytical chemistryPolymerConductivityPolypyrrolechemistry.chemical_compoundchemistryElectrodeElectrochemistryThin filmComposite materialDeposition (law)Chemically modified electrodeElectrochimica Acta
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Synthesis of a New pH-Dependent Ligand: Conformational and Complexation Studies

2003

A new macrocyclic ligand, 3, which exhibits pH-induced conformational changes, has been prepared. This ligand consists of a crown ether derived from a trans-anti-trans 1,2,4,5-tetrasubstituted cyclohexane. Due to the stereochemistry of the substituents on the carbocyclic ring, two different low-energy conformations of the crown ether are possible. Ligand 3 has been studied in solution by 1H NMR spectroscopy at different values of pH and temperature, showing that the conformation of the crown ether, and thus its complexing ability, is strongly pH-dependent. The solid-state structure of the ligand has been determined by X-ray diffraction.

chemistry.chemical_classificationCrystallography1h nmr spectroscopychemistry.chemical_compoundchemistryCyclohexaneStereochemistryPh dependentGeneral ChemistryMacrocyclic ligandLigand (biochemistry)Ring (chemistry)Crown etherSupramolecular Chemistry
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Cation and Anion Coordination Chemistry of Palladium(II) with Polyazacycloalkanes. Thermodynamic and Structural Studies

1992

The interaction of PdCI2 4 - with the macrocyclic ligands of the series [3k]aneNk has been studied both in solution and in the solid state. [18]aneN6 and [21]aneN7 form both mono- and binuclear Pd2+ complexes, whose stability constants have been determined in 0.5 mol dm-3 NaCI at 298.15 K. [21]aneN7 also forms, in solution, a trinuclear species in which an amino group deprotonates to bridge two Pd2+ ions, as observed in the solid state. The crystal structure of the complexes [Pd2([18]aneN6)Cl2][CIO4]2 and [Pd3[21]aneN7)CI3][CIO4]2 ⋅ H2O have been solved by single crystal X-ray analysis. C12H30N6CI4O8Pd2: monoclinic, space group C2/m, a = 10.876(2), b = 18.117(2), c = 7.043(2) A, s = 113.78(…

chemistry.chemical_classificationCrystallographyDeprotonationchemistryStereochemistryX-ray crystallographyOrthorhombic crystal systemCrystal structureTriclinic crystal systemSingle crystalCoordination complexMonoclinic crystal system
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pH-Dependent ligands as carriers in transport experiments

2004

Abstract Conformationally pH-regulated ligands have been used as carriers in transport experiments. The experiments were carried out through bulky membranes and the pH at the source phase and at the receiving phase were modified to study the ability of ligands to act as pH-regulated carriers. The influence of pH on transport efficiency seems to be related to its influence on conformational equilibrium. X-ray determination of one precursor compound has been useful for determining the stereochemistry of one of the carriers. To cite this article: A.M. Costero et al., C. R. Chimie 7 (2004).

chemistry.chemical_classificationCyclohexaneStereochemistryGeneral Chemical EngineeringPh dependentGeneral ChemistryCycloalkanechemistry.chemical_compoundMembraneHydrocarbonchemistryComputational chemistryPhase (matter)X-ray crystallographyCrown etherComptes Rendus Chimie
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1H NMR studies of paramagnetic ferricytochrome c-551 from Pseudomonas aeruginosa at high pH: The role of histidine 16 in the spin transition

2005

Abstract Cytochrome c-551 from the mesophile Pseudomonas aeruginosa is an electronic transfer protein that contains 82 amino-acid residues and a c-type heme as the prosthetic group with low spin Fe(II) in the reduced form and low spin Fe(III) in the oxidized form of cytochrome c-551. We have studied the electronic properties of ferricytochrome c-551 from P. aeruginosa at high pH (9–11.4) by means of paramagnetic 1H NMR spectra and the T1 and T2 values of isotropically shifted proton resonances. We have also analyzed the temperature dependence of the hyperfine-shifts. Resonance assignment of some signals was based on 2D saturation transfer experiments, EXSY. These results indicate the existe…

chemistry.chemical_classificationCytochromebiologySpin transitionAnalytical chemistryInorganic Chemistrychemistry.chemical_compoundCrystallographyDeprotonationchemistrySpin crossoverMaterials ChemistryMetalloproteinbiology.proteinProton NMRPhysical and Theoretical ChemistryHemeTwo-dimensional nuclear magnetic resonance spectroscopyPolyhedron
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CuIIand ZnIICoordination Chemistry of Pyrazole‐Containing Polyamine Receptors − Influence of the Hydrocarbon Side Chain Length on the Metal Coordinat…

2004

The synthesis of a new macrocyclic receptor (L 4 ) containing two 3,5-dimethylpyrazole units connected by dipropylenetriamine bridges is reported for the first time; pH-metric titrations indicate that L 4 shows six protonation steps in the pH range 2-11. In the absence of metal ions, the pyrazole moieties are not involved in acid-base processes in this pH range. Addition of Cu I I and Zn I I results in deprotonation of the pyrazole moieties which act as bis(monodentate) η 1 :η 1 ligands. This induced deprotonation occurs at higher pH values than in the complexes of the analogous ligand containing diethylenetriamine bridges (L 1 ). The crystal structures of [Cu 2 (H - 2 L 4 )](ClO 4 ) 2 and …

chemistry.chemical_classificationDenticityChemistryStereochemistryLigandPyrazoleCoordination complexInorganic ChemistryCrystallographyTrigonal bipyramidal molecular geometrychemistry.chemical_compoundDeprotonationDiethylenetriamineCoordination geometryEuropean Journal of Inorganic Chemistry
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