Search results for "Comproportionation"

showing 5 items of 5 documents

Electro- and magneto-electrochemistry of zeolite Y- and MCM-41-associated bipyrylium ion

2005

Abstract The electrochemical response of bipyrylium bication [1,4-bis(3,5-diphenyl-4-pyrylium)phenylene] associated with Y and MCM-41 aluminosilicates (BTP@Y and BTP@MCM, respectively) is described using polymer-film electrodes immersed into Et 4 N +  + MeCN and Bu 4 N +  + MeCN electrolytes. BTP@MCM provides a solution-like response in all electrolytes consisting in two successive strongly comproportionation mediated one-electron reduction processes near to +0.05 and −0.12 V vs. Ag|AgCl. The response of BTP@Y in Bu 4 N +  + MeCN is restricted to a unique reduction process near to −0.40 V, while in Et 4 N +  + MeCN, it differs significantly: here, two reduction processes at −0.22 and −0.36 …

General Chemical EngineeringInorganic chemistryComproportionationElectrolyteElectrochemistryRedoxAnalytical Chemistrychemistry.chemical_compoundCrystallographyElectron transferchemistryPhenyleneElectrochemistryMagnetoelectrochemistryAcetonitrileJournal of Electroanalytical Chemistry
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Synthesis, characterization and crystal structure of 2-dicyanomethylene-1,3-bis(ferrocenylmethyl)-1,3-diazolidine

1993

By reaction of N,N′-ethylenebis(ferrocenylmethylamine)1 with tetracyanoethylene in dichloromethane the yellow compound 2-dicyanomethylene-1,3-bis(ferrocenylmethyl)-1,3-diazolidine 2 can be isolated. The single-crystal structure of 2 has been determined. It crystallizes in the non-centrosymmetric trigonal space group P3221, a= 12.255(2), c= 13.831(7)A, Z= 3. Refinement of the atomic parameters by least-squares techniques gave a final R factor of 0.038 (R′= 0.034) for 1782 observed reflections having I > 2.5δ(I). Anomalous values of the bond distances and the vinyl carbon chemical shift in the 13C NMR spectrum of 2 are explained on the basis of a polarization due to a combination of the elect…

chemistry.chemical_compoundCrystallographychemistryStereochemistryDiamineX-ray crystallographyMoleculeGeneral ChemistryComproportionationDifferential pulse voltammetryCrystal structureTetracyanoethyleneCarbon-13 NMRJ. Chem. Soc., Dalton Trans.
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Electrochemical Monitoring of Compartmentalization Effects in the Stability of Meisenheimer Anions Supported in Hydrotalcite and X and Y Zeolites

2005

Meisenheimer anions (MS - ) derived from 2,4-dinitroaniline are stabilized into Li + - and Na + -exchanged zeolites X and Y forming alkali ion-MS ion pairs. Upon attachment of the zeolites to polymer film electrodes immersedinto Et 4 N + /MeCN and Li + /MeCN electrolytes, boundary-associated MS - ions display two oxidation processes at +0.40 and +0.65 V vs. AgCl/Ag. This response sharply contrasts with that recorded for MS - in solution and incorporated within hydrotalcite, for which a unique oxidation peak at +0.35 V is recorded. The electrochemistry of zeolite-associated MS - can be described in terms of an unusual electron-transfer/ chemical reaction/electron-transfer/comproportionation …

HydrotalciteRenewable Energy Sustainability and the EnvironmentChemistryInorganic chemistryComproportionationElectrolyteCondensed Matter PhysicsElectrochemistryAlkali metalChemical reactionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDeprotonationMaterials ChemistryElectrochemistryChemical stabilityJournal of The Electrochemical Society
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A kinetic model for the oxidation of benzenethiol catalyzed by the [MoVIO2(O2CC(S)(C6H5)2)2]2− complex intercalated in a Zn(II)–Al(III) layered doubl…

2009

Abstract The heterogeneous oxidation of benzenethiol catalyzed by the dianionic bis(2-sulfanyl-2,2-diphenylethanoxycarbonyl) dioxomolybdate (VI) complex intercalated into a Zn(II)–Al(III) layered double hydroxide (LDH) host have been investigated under aerobic conditions. The kinetics of the system has been analysed in detail. In ethanol, the benzenethiol is cleanly oxidized to diphenyl disulfide in the acidic media provided by the protonic resin Amberlite IR-120(H). The reaction is second-order in benzenethiol, and the apparent rate coefficient has been found to be proportional to the catalyst weight and inversely proportional to the initial concentration of the substrate. A catalytic cycl…

Diphenyl disulfideProcess Chemistry and TechnologyInorganic chemistryComproportionationRate-determining stepMedicinal chemistryCatalysisCatalysischemistry.chemical_compoundchemistryCatalytic cycleHydroperoxylOxidation stateHydroxidePhysical and Theoretical ChemistryJournal of Molecular Catalysis A: Chemical
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Mono-organotin(IV) and tin(IV) derivatives of 2-mercaptopyridine and 2-mercaptopyrimidine: X-ray structures of methyl-tris(2-pyridinethiolato)tin(IV)…

1997

Mono-organotin(IV) and tin(IV) derivatives of 2-mercaptopyridine (HSPy) and 2-mercaptopyrimidine (HSPym), RSnL 3 (R=Me, n-Bu, Ph; L=SPy, SPym; R=Bz=benzyl, o-CIBz, oClC 6 H 4 , p-ClC 6 H 4 , o-tolyl, p-tolyl; L=SPy), RSnCIL 2 (R=Me, n-Bu, Ph; L=SPy, SPym), RSnCI 2 L (R=Me, n-Bu; L=SPy, SPym) and SnCI 4-n L n (L=SPy, SPym; n=2,4) were obtained from RSnCI 3 or SnCI 4 and NaL or by neutralization (R=Ph,p-tolyl; L=SPy, SPym). RSnCIL 2 and RSnCI 2 L were better prepared by comproportionation of RSnCI 3 and RSnL 3 . MeSn(Spy) 3 and PhSn(SPy) 3 .1.5CHCI 3 crystals, as determined by single-crystal X-ray diffraction, are monoclinic. In the discrete monomeric RSn(SPy) 3 units, three bidentate SPy lig…

DenticityStereochemistry2-Mercaptopyridinechemistry.chemical_elementGeneral ChemistryComproportionationCrystal structureInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundCrystallographyPentagonal bipyramidal molecular geometryOctahedronchemistryTinApplied Organometallic Chemistry
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