Search results for "Proton"

showing 10 items of 5886 documents

Solution behaviour and relative stability of the complexes [MCl2(RNCHCHNR)] and [MCl2(py-2-CHNR)] (M=Pd, Pt;R=C6H4OMe-p)

1988

Abstract Even though the α-diimino complexes [MCl 2 (RNCHCHNR)] and [MCl 2 (py-2-CHNR)] (M=Pd, Pt;R=C 6 H 4 OMe- p ) are poorly soluble in chlorinated solvents, such as chloroform and 1,2-dichloroethane, or in acetonitrile, the electronic and 1 H NMR spectra indicate that these compounds are generally present as undissociate monomers with σ, σ′- N,N′ chelate N-ligands in dilute solutions. Only for [PdCl 2 (RNCHCHNR)], some dissociation of the α-diimine occurs in acetonitrile. In dimethylsulfoxide, where the solubility is much higher, no dissociation is observed for the pyridine-2-carbaldimine complexes [MCl 2 (py-2-CHNR)], whereas the 1,2-bis(imino) ethane derivatives [MCl 2 (RNCH…

Substitution reactionDenticityChloroformChemistryStereochemistryNuclear magnetic resonance spectroscopyMedicinal chemistryDissociation (chemistry)Inorganic Chemistrychemistry.chemical_compoundMaterials ChemistryProton NMRPhysical and Theoretical ChemistrySolvent effectsAcetonitrileInorganica Chimica Acta
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Preparation and protonation of 2-pyrimidyl- and 2-pyrazylpalladium(II) complexes

1985

Abstract The oxidative addition of 2-chloropyrimidine or 2-chloropyrazine to [Pd(PPh 3 ) 4 ] yields a mixture of trans -[PdCl(C 4 H 3 N 2 - C 2 )(PPh 3 ) 2 ] (I) and [PdCl(μ-C 4 H 3 N 2 - C 2 , N 1 )(PPh 3 (II) (C 4 H 3 N 2 = 2-pyrimidyl or 2-pyrazyl group). The mononuclear complexes I are quantitatively converted into the binuclear species II upon treatment with H 2 O 2 . The reaction of II with HCl gives the N -monoprotonated derivatives cis -[PdCl 2 (C 4 H 4 N 2 - C 2 )(PPh 3 )] (III), from which the cationic complexes trans -[PdCl(C 4 H 4 N 2 - C 2 )(L) (L = PPh 3 , IV; PMe 2 Ph, V; PEt 3 , VI) can be prepared by ligand substitution reactions. Reversible proton dissociation occurs in so…

Substitution reactionStereochemistryChemistryLigandOrganic ChemistryProtonationNuclear magnetic resonance spectroscopyBiochemistryOxidative additionInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryProton NMRMoietyPhysical and Theoretical ChemistryTriphenylphosphineJournal of Organometallic Chemistry
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Chalcogenide-capped triiron clusters [Fe3(CO)9(μ3-E)2], [Fe3(CO)7(μ3-CO)(μ3-E)(μ-dppm)] and [Fe3(CO)7(μ3-E)2(μ-dppm)] (E = S, Se) as proton-reduction…

2019

Chalcogenide-capped triiron clusters [Fe3(CO)7(μ3-CO)(μ3-E)(μ-dppm)] and [Fe3(CO)7(μ3-E)2(μ-dppm)] (E = S, Se) have been examined as proton-reduction catalysts. Protonation studies show that [Fe3(CO)9(μ3-E)2] are unaffected by strong acids. Mono-capped [Fe3(CO)7(μ3-CO)(μ3-E)(μ-dppm)] react with HBF4.Et2O but changes in IR spectra are attributed to BF3 binding to the face-capping carbonyl, while bicapped [Fe3(CO)7(μ3-E)2(μ-dppm)] are protonated but in a process that is not catalytically important. DFT calculations are presented to support these protonation studies. Cyclic voltammetry shows that [Fe3(CO)9(μ3-Se)2] exhibits two reduction waves, and upon addition of strong acids, proton-reducti…

SulfideInfrared spectroscopyProtonationorganometalliyhdisteetSulfonic acid010402 general chemistryElectrochemistry01 natural sciencesBiochemistryMedicinal chemistryCatalysisInorganic Chemistrychalcogenidechemistry.chemical_compoundSelenideElectrochemistryMaterials ChemistryPhysical and Theoretical Chemistryclusterta116proton-reductionchemistry.chemical_classification010405 organic chemistryChalcogenideOrganic Chemistrytriironsähkökemia0104 chemical scienceselectrochemistrychemistryClusterTriironProton-reductionCyclic voltammetryJournal of Organometallic Chemistry
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Light-driven proton transport of bacteriorhodopsin incorporated into long-term stable liposomes of a polymerizable sulfolipid

1983

Abstract The chromoprotein bacteriorhodopsin from Halobacterium halobium has been incorporated into liposomes made of a fully synthetic, polymerizable lipid. Bacteriorhodopsin is found to be active in these polymer liposomes. The advantage in the use of such polymer systems concerning long-term stability in comparison with liposomes made of natural lipid is demonstrated.

SulfolipidBiophysicsBacteriorhodopsinHalobacterium halobiumBiochemistrychemistry.chemical_compoundStructural BiologyChromoproteinProton transportGeneticsOrganic chemistryLight-driven proton pumpLong-term stabilityMolecular Biologychemistry.chemical_classificationLiposomebiologyBacteriorhodopsinCell BiologyPolymerLiposomechemistrybiological sciencesbiology.proteinLight drivenBiophysicsPolymerizable synthetic lipidFEBS Letters
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1H NMR and UV-vis spectroscopic characterization of sulfonamide complexes of nickek(II)-carbonic anhydrase. Resonance assignments based on NOE effects

1992

The binding of acetazolamide, p-fluorobenzensulfonamide, p-toluenesulfonamide, and sulfanilamide to nickel(II)-substituted carbonic anhydrase II has been studied by 1H NMR and electronic absorption spectroscopies. These inhibitors bind to the metal ion forming 1:1 complexes and their affinity constants were determined. The 1H NMR spectra of the formed complexes show a number of isotropically shifted signals corresponding to the histidine ligands. The complexes with benzene-sulfonamides gave rise to very similar 1H NMR spectra. The NMR data suggest that these aromatic sulfonamides bind to the metal ion altering its coordination sphere. In addition, from the temperature dependence of 1H NMR s…

SulfonamidesConformational changeMagnetic Resonance SpectroscopyCoordination sphereProtein ConformationCarbon-13 NMR satelliteChemistryStereochemistryCarbonic anhydrase IINuclear magnetic resonance spectroscopy of nucleic acidsNuclear magnetic resonance spectroscopyBiochemistryAdductAcetazolamideInorganic ChemistryCrystallographyNickelSpectrophotometryProton NMRAnimalsCattleSpectrophotometry UltravioletCarbonic AnhydrasesProtein BindingJournal of Inorganic Biochemistry
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Inhibitoren der Korrosion (9) Nachweis der Sekundärinhibitoren bei einigen Sulfoxiden, Triphenylarsinoxid und einigen Sulfoniumsalzen

1971

Die Schutzwerte von Dibenzylsulf-oxyd und strukturell verwandten Ver-bindungen sowie von Triphenylarsin-oxyd werden bestimmt. Sulfoxyde und Arsinoxyde werden (a) nach Protonierung in die kathodischen Bereiche gefuhrt und (b) nach Elektronenaufnahme in die ko-ordinationsfahigen Sekundarinhibitoren (Thioather und tert. Arsine) umgewan-delt. Die Sekundarinhibitoren ziehen entweder auf das Metall auf und unter-drucken dann die Auflosung des Eisens oder werden nicht am Metall fixiert (z. B. Diphenylsulfid) und entfalten dann keinen Schutz. Im Falle des Dibenzyl-sulfoxyds konnen ca. 90% des einge-setzten Dibenzylsulfoxyds als Dibenzyl-sulfid vom Eisen abgelost werden; 16% an unverandertem Dibenzy…

SulfoniumMechanical EngineeringMetals and AlloysOxideProtonationSulfoxideGeneral MedicineSurfaces Coatings and FilmsMetalchemistry.chemical_compoundArsinechemistryMechanics of MaterialsHydrogen Sulfatevisual_artPolymer chemistryMaterials ChemistryDibenzyl sulfidevisual_art.visual_art_mediumEnvironmental ChemistryMaterials and Corrosion/Werkstoffe und Korrosion
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Photoredox-catalyzed synthesis of N-unsubstituted enaminosulfones from vinyl azides and sulfinates

2021

Abstract A metal-free visible light photoredox-catalyzed synthesis of N-unsubstituted enaminosulfones from vinyl azides and sodium sulfinates in moderate to high yields is described. The reaction proceeds in ethanol and uses eosin Y as a readily available photocatalyst in combination with nitrobenzene as an electron shuttle. Taking into account the number of steps involved (generation of the sulfonyl radical, its addition to the double bond, elimination of molecular nitrogen with formation of an iminyl radical, followed by its reduction and protonation) as well as the number of redox-active reaction partners involved, the selectivity of the process is quite impressive.

Sulfonylchemistry.chemical_classificationDouble bond010405 organic chemistryChemistryOrganic ChemistryProtonation010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistry0104 chemical sciencesCatalysisNitrobenzenechemistry.chemical_compoundDrug DiscoveryPhotocatalysisSelectivityEosin YTetrahedron Letters
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Neutrino emission due to Cooper pairing of protons in cooling neutron stars: Collective effects

2000

The process of neutrino-pair radiation due to formation and breaking of Cooper pairs of protons in superconducting cores of neutron stars is considered with taking into account of the electromagnetic coupling of protons to ambient electrons. It is shown that plasma polarization strongly modifies the effective vector weak current of protons. Collective response of ambient electrons to the proton quantum transition contributes coherently to the complete interaction with the neutrino field and enhances the rate of neutrino-pair production by two orders of magnitude.

SuperconductivityPhysicsNuclear and High Energy PhysicsParticle physicsProtonNuclear TheoryFOS: Physical sciencesElectronRadiationNuclear physicsNeutron starHigh Energy Physics - PhenomenologyHigh Energy Physics - Phenomenology (hep-ph)PairingNeutrinoCooper pairNuclear Experiment
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Highly sensitive superconducting circuits at ∼700 kHz with tunable quality factors for image-current detection of single trapped antiprotons

2016

We developed highly-sensitive image-current detection systems based on superconducting toroidal coils and ultra-low noise amplifiers for non-destructive measurements of the axial frequencies (550$\sim$800$\,$kHz) of single antiprotons stored in a cryogenic multi-Penning-trap system. The unloaded superconducting tuned circuits show quality factors of up to 500$\,$000, which corresponds to a factor of 10 improvement compared to our previously used solenoidal designs. Connected to ultra-low noise amplifiers and the trap system, signal-to-noise-ratios of 30$\,$dB at quality factors of > 20$\,$000 are achieved. In addition, we have developed a superconducting switch which allows continuous tu…

SuperconductivityPhysicsSpeichertechnik - Abteilung BlaumPhysics - Instrumentation and DetectorsSolenoidal vector fieldbusiness.industryAmplifierDetectorFOS: Physical sciencesInstrumentation and Detectors (physics.ins-det)01 natural sciencesNoise (electronics)010305 fluids & plasmasQuality (physics)Antiproton0103 physical sciencesOptoelectronicsDetectors and Experimental Techniques010306 general physicsbusinessphysics.ins-detInstrumentationElectronic circuit
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How deprotonation changes molecular self-assembly – an AFM study in liquid environment

2013

We study the influence of Alizarin Red S deprotonation on molecular self-assembly at the solid-liquid interface of the natural cleavage plane of calcite immersed in aqueous solution. To elucidate the adsorption details, we perform pH dependent high-resolution atomic force microscopy measurements. When Alizarin Red S is deposited onto calcite(10.4) in a liquid environment at an acidic pH of 5, weakly bound, ordered islands with a (3 x 3) superstructure are observed. A sharp structural transition is revealed when increasing the pH above 8. Above this pH, stable needle-like structures oriented along the [01.0] direction form on the surface. Comparing these results with potentiometric titration…

SuperstructureAqueous solutionChemistryPotentiometric titrationInorganic chemistryALIZARIN REDProtonationGeneral ChemistryCondensed Matter Physics530CrystallographyDeprotonationAdsorptionMolecular self-assemblySoft Matter
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