Search results for "Chlorate"

showing 10 items of 647 documents

Dehydrogenation versus Oxygenation in Two-Electron and Four-Electron Reduction of Dioxygen by 9-Alkyl-10-methyl-9,10-dihydroacridines Catalyzed by Mo…

2004

Dehydrogenation of 10-methyl-9,10-dihydroacridine (AcrH(2)) by dioxygen (O(2)) proceeds efficiently, accompanied by the two-electron and four-electron reduction of O(2) to produce H(2)O(2) and H(2)O, which are effectively catalyzed by monomeric cobalt porphyrins and cofacial dicobalt porphyrins in the presence of perchloric acid (HClO(4)) in acetonitrile (MeCN) and benzonitrile (PhCN), respectively. The cobalt porphyrin catalyzed two-electron reduction of O(2) also occurs efficiently by 9-alkyl-10-methyl-9,10-dihydroacridines (AcrHR; R = Me, Et, and CH(2)COOEt) to yield 9-alkyl-10-methylacridinium ion (AcrR+) and H(2)O(2). In the case of R = Bu(t) and CMe(2)COOMe, however, the catalytic two…

Metalloporphyrinschemistry.chemical_elementElectronsReaction intermediatePhotochemistryBiochemistryMedicinal chemistryCatalysisCatalysischemistry.chemical_compoundColloid and Surface ChemistryDehydrogenationPerchloric acidAlkylchemistry.chemical_classificationPerchloratesChemistryCobaltGeneral ChemistryNADPorphyrinKineticsBenzonitrileAcridinesHydrogenationOxidation-ReductionCobaltJournal of the American Chemical Society
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Ferromagnetic Cu(II)4, Co(II)4, and Ni(II)6 azido complexes derived from metal-assisted methanolysis of di-2,6-(2-pyridylcarbonyl)pyridine.

2009

Reaction of copper(II) perchlorate with di-2,6-(2-pyridylcarbonyl)pyridine (pyCOpyCOpy, dpcp) in the presence of sodium azide yields complex [Cu(4)(N(3))(2){pyC(OMe)(O)pyC(OMe)(O)py}(2)(MeOH)(2)](ClO(4)) x 2 MeOH (1 x 2 MeOH), which crystallizes in the monoclinic P2(1)/c space group. Similar reaction of cobalt(II) nitrate yields complex [Co(4)(N(3))(2)(NO(3))(2){pyC(OMe)(O)pyC(OMe)(O)py}(2)] x 0.5 MeOH (2 x 0.5 MeOH) which crystallizes in the monoclinic I2/m space group. Reaction of nickel(II) perchlorate yields complex [Ni(6)(CO(3))(N(3))(6){pyCOpyC(O)(OMe)py}(3)(MeOH)(2)(H(2)O)][Ni(6)(CO(3))(N(3))(6){pyCOpyC(O)(OMe)py}(3) (MeOH)(3)](ClO(4))(2) x 1.8 MeOH (3 x 1.8 MeOH), which crystallizes…

Models MolecularChemistryStereochemistryPyridinesCyclohexane conformationTemperaturechemistry.chemical_elementCobaltCrystallography X-RayMagnetic susceptibilityInorganic ChemistryPerchloratechemistry.chemical_compoundNickelCrystallographyMagneticsDeprotonationCubaneNickelPyridineOrganometallic CompoundsPhysical and Theoretical ChemistryCopperMonoclinic crystal systemInorganic chemistry
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Synthesis, characterization, cellular uptake and interaction with native DNA of a bis(pyridyl)-1,2,4-oxadiazole copper(II) complex

2010

The copper(II) complex of 3,5-bis(2'-pyridyl)-1,2,4-oxadiazole was synthesized and characterized. X-Ray crystallography revealed that the complex consists of a discrete [Cu(3,5-bis(2'-pyridyl)-1,2,4-oxadiazole)(2)(H(2)O)(2)](2+) cation and two ClO(4)(-) anions. The Cu(II) coordination sphere has a distorted octahedral geometry and each ligand chelates the copper ion through the N(4) nitrogen of the oxadiazole ring and the nitrogen of one pyridine moiety. The coordinated water molecules are in cis position and each of them is H-bonded to the 5-pyridyl nitrogen of the oxadiazole ligand and to an oxygen of the perchlorate anion. Biological assays showed that, despite the free ligand not being …

Models MolecularCircular dichroismCoordination sphereheterocylces metal complex DNA binders anti-tumoralsCell SurvivalPyridinesStereochemistrychemistry.chemical_elementOxadiazoleLigandsInorganic Chemistrychemistry.chemical_compoundPerchlorateCell Line TumorOctahedral molecular geometryOrganometallic CompoundsHumansOxadiazolesChemistryLigandDNASettore CHIM/06 - Chimica OrganicaCopperBinding constantCrystallographySettore CHIM/03 - Chimica Generale E InorganicaCopper
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Mössbauer effect study of the electronic ground state of iron(II)in tris(2-chlorophenanthroline)iron(II) perchlorate

1976

Abstract Mossbauer spectra of [Fe(2-Cl-phen) 3 ](ClO 4 ) 2 ·H 2 O have been measured in the temperature range 293 − 5 K. The spectra indicate that the iron atom in this compound possesses a spin quintet ground state throughout the temperature range under study, in contradiction to the suggested high spin-low spin transition, which has been concluded from a magnetic susceptibility study by other authors. From a theoretical analysis of the temperature dependence of the quadrupole splitting, with trigonal distortion, spin-orbit coupling, and effects of covalency taken into account, the ground term of iron(II) in this compound has been elucidated as being 5 A 1 ( 5 T 2g ), separated from the 5 …

Mössbauer effectCondensed matter physicsChemistryAnalytical chemistrySpin transitionQuadrupole splittingAtmospheric temperature rangeMagnetic susceptibilityInorganic ChemistryPerchloratechemistry.chemical_compoundMaterials ChemistryCondensed Matter::Strongly Correlated ElectronsPhysical and Theoretical ChemistryGround stateElectric field gradientInorganica Chimica Acta
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Nucleophilic attack by 2-pyridylpalladium(II) and platinum(II) complexes on the organic chlorides ClCH2R (R  COMe, CN, Ph, Cl)

1992

Abstract The 2-pyridyl complexes trans-[MCl(C5H4NC2)(PPh3)2] (M = Pd, 1a; M = Pt, 1b), [MCl(C5H4NC2)(dppe)] (M = Pd, 2a; M = Pt, 2b) and [M(dmtc)(C5H4NC2) (PPh3)] (M = Pd, 3a; M = Pt,3b) react with the chlorides ClCH2R(R  COMe, CN, Ph) to give cationic products containing the 2-pyridylium ligands (1-CH2R)C5H4NC2. The rate of nucleophilic displacement of the chloride ion from ClCH2R depends on the central metal (Pt > Pd), on the coordination geometry (1 ~ 3) and on the substituent R (COMe > CN > Ph for the reactions with 3b). Like 1b and 2b, complex 3b also reacts with dichloromethane to give [Pt(dmtc){(1-CH2Cl)C5H4NC2}(PPh3)]+. The reaction of the binuclear compound [{PdCl(μ-C5H4NC2,…

NitrileStereochemistryOrganic ChemistryCationic polymerizationchemistry.chemical_elementBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundPerchlorateChloroacetonechemistryNucleophileMaterials ChemistryNucleophilic substitutionPhysical and Theoretical ChemistryPlatinumCoordination geometryJournal of Organometallic Chemistry
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Effect of Lithium Perchlorate on the Kinetics of the Anionic Polymerization of Methyl Methacrylate in Tetrahydrofuran

1999

The kinetics of the anionic polymerization of methyl methacrylate in the presence of lithium perchlorate (LiClO 4 ) are investigated in THF using 1,1-diphenylhexyllithium as initiator in a flow-tube reactor between -30 and 0 °C. The rate constants of propagation determined in the presence of LiClO 4 are lower than those obtained in the absence of the salt, similar to the effect observed for LiCl. For propagation, the reaction order with respect to active center concentration is found to be 0.5 in both cases, which indicates that LiClO 4 does not effectively perturb the aggregation of the enolate ion pair. The formation of various mixed aggregates is proposed. The polydispersity index of the…

Order of reactionPolymers and PlasticsOrganic ChemistryInorganic chemistryKineticsSolution polymerizationLithium perchlorateInorganic Chemistrychemistry.chemical_compoundAnionic addition polymerizationReaction rate constantchemistryMaterials ChemistryMethyl methacrylateTetrahydrofuranMacromolecules
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Complex formation of Tb3+ with glycolate, D-gluconate and α-isosaccharinate in neutral aqueous perchlorate solutions

2003

Summary An electromigration technique was used for measurements of metal-ligand formation constants of non-carrier-free 160Tb3+ with glycolate, D-gluconate and α-isosaccharinate ligands. The overall ion mobilities of Tb at different concentrations of the ligands were measured in chemically inert perchlorate solutions (pH 7 and T= 298.1K) with an overall ionic strength μ = 0.1. The stepwise stoichiometric stability constants are: Tb3+/glycolate: log K 1=2.72(18), log K 2=1.73(19), log K 3= 1.12(17), Tb3+/D-gluconate: log K 1=2.96(11), log K 2=2.60(11), log K 3=1.13(9), Tb3+/α-ISA: log K 1=3.07(8), log K 2 = 2.69(11), log K 3 = 1.80(12).

Perchloratechemistry.chemical_compoundAqueous solutionchemistryD-gluconateIonic strengthStability constants of complexesStereochemistryComplex formationPhysical chemistryPhysical and Theoretical ChemistryStoichiometryIonRadiochimica Acta
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Structure and properties of 2-cyanopyridinium perchlorate [2-CNPyH][ClO4]

2006

The crystal structure of 2-cyanopyridinium perchlorate, [2-CNPyH][ClO4], has been determined at 100 (phase II) and 293 K (phase I). It is monoclinic P 21 at 100 K and orthorhombic P 212121 at 293 K. The dynamic properties of the crystal were studied by differential scanning calorimetry, dilatometry, pyroelectric, dielectric, proton (1H NMR), chlorine (35Cl NMR) magnetic resonance spectroscopies and the infrared method. The crystal undergoes a structural phase transition () at 170 K characterized by a complex mechanism involving both 'order–disorder' and 'displacive' contributions. It reveals pyroelectric properties below 170 K. The dielectric relaxation existing over phase I is due to the m…

Phase transitionChemistryDielectricCrystal structureCondensed Matter PhysicsCrystalPerchloratechemistry.chemical_compoundCrystallographyNuclear magnetic resonancePhase (matter)General Materials ScienceOrthorhombic crystal systemMonoclinic crystal systemJournal of Physics: Condensed Matter
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Static and MAS 35CI NMR and Molecular Motions of ClO −4 Ions in the Various Phases of Multimethylammonium Perchlorates

1986

Static and MAS*) 35CI NMR data of CIO−4 ions in the low-, intermediate- and high-temperature phases of trimethylammonium, dimethylammonium and monomethylammonium perchlorates are reported. The observed solid-solid phase transitions are interrelated with the motional state of the perchlorate ions. In the low-temperature phase III of trimethylammonium perchlorate there is an anisotropic motion of the ClO−4 ions with a constant quadrupole frequency of 185 kHz and an increasing value of the asymmetry parameter when approaching phase transition III-II. The activation energy for this motion is found to be 44.3 kj/mol. At the transition III-II the ClO−4 ions gain orientational degrees of freedom m…

Phase transitionPerchloratechemistry.chemical_compoundMagic angleNuclear magnetic resonanceChemistryGeneral Chemical EngineeringPhase (matter)QuadrupolePhysical chemistryNuclear magnetic resonance spectroscopyActivation energyIonBerichte der Bunsengesellschaft für physikalische Chemie
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Calix[4]arenes as Selective Extracting Agents. An NMR Dynamic and Conformational Investigation of the Lanthanide(III) and Thorium(IV) Complexes

2000

The lanthanide and Th4+ complexes with calix[4]arene ligands substituted either on the narrow or at the wide rim by four coordinating groups behave totally differently as shown by an NMR investigation of the dia- and paramagnetic complexes. Solutions of complexes were prepared by reacting anhydrous metal perchlorate salts with the ligands in dry acetonitrile (CAUTION). Relaxation time T1 titrations of acetonitrile solutions of Gd3+ by calixarenes indicate that ligands subsituted on the narrow rim form stable 1:1 complexes whether they feature four amide groups (1) or four phosphine oxide functions. In contrast, a ligand substituted by four (carbamoylmethyl)-diphenylphosphine oxide moieties …

Phosphine oxideLanthanideLigandInorganic chemistryInorganic Chemistrychemistry.chemical_compoundCrystallographyParamagnetismPerchloratechemistryAmideChelationPhysical and Theoretical ChemistryAcetonitrileInorganic Chemistry
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