Search results for "Complexes."

showing 10 items of 857 documents

A magnetic self-contained thermochromic system with convenient temperature range

2019

A new ionic liquid with sugar-based ligand has been prepared and used to coordinate cobalt(II), at low loading, in an ionic liquid solution. The system obtained reveals magnetic switching and marked thermochromism in solution/polymer films over a convenient temperature range (20–60 °C). This system is self-contained, devoid of any volatile substances, and reproducible over multiple thermal cycles. The colour change can be attributed to a change in the coordination geometry from octahedral (pink) at room temperature to tetrahedral (blue) on warming, monitored by 59Co NMR spectroscopy, which was used for the first time to study the change. This material may find applications in stimuli-respon…

chemistry.chemical_classificationThermochromismIonic liquids thermochromic systemMaterials science010405 organic chemistryAnalytical chemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopyPolymercobalt complexesSettore CHIM/06 - Chimica OrganicaAtmospheric temperature range010402 general chemistry01 natural sciencesPollution0104 chemical scienceschemistry.chemical_compoundOctahedronchemistry13. Climate actionIonic liquidEnvironmental ChemistryCobaltCoordination geometry
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Spin Switching with Triazolate-Strapped Ferrous Porphyrins

2019

Fe(III) porphyrins bridged with 1,2,3-triazole ligands were synthesized. Upon deprotonation, the triazolate ion coordinates to the Fe(III) ion, forming an overall neutral high-spin Fe(III) porphyrin in which the triazolate serves both as an axial ligand and as the counterion. The second axial coordination site is activated for coordination and binds p-methoxypyridine, forming a six-coordinate low-spin complex. Upon addition of a phenylazopyridine as a photodissociable ligand, the spin state of the complex can be reversibly switched with ultraviolet and visible light. The system provides the basis for the development of switchable catalase- and peroxidase-type catalysts and molecular spin sw…

chemistry.chemical_classificationkemiallinen synteesiSpin states010405 organic chemistryLigandkompleksiyhdisteet010402 general chemistry01 natural sciencesPorphyrin0104 chemical sciencesIonCatalysisInorganic Chemistrychemistry.chemical_compoundCrystallographyDeprotonationchemistrycoordination complexesPhysical and Theoretical ChemistryCounterionta116chemical synthesisVisible spectrumInorganic Chemistry
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Structural characterization of U(VI) surface complexes on kaolinite in the presence of humic acid using EXAFS spectroscopy.

2007

To determine the influence of humic acid (HA), pH, and presence of atmospheric CO2 on the sorption of U(VI) onto kaolinite, the structure of the surface complexes was studied by U L III-edge extended X-ray absorption fine structure (EXAFS) spectroscopy. The best fits to the experimental EXAFS data were obtained by including two uranium coordination shells with two axial (O ax) and five equatorial (O eq) oxygen atoms at 1.77+/-0.02 and 2.34+/-0.02 A, respectively, and two coordination shells with one Al/Si atom each at 3.1 and 3.3 A. As in the case of the binary system U(VI)-kaolinite, uranium forms inner-sphere surface complexes by edge sharing with aluminum octahedra and/or silicon tetrahe…

chemistry.chemical_classificationsorptionkaoliniteExtended X-ray absorption fine structureAnalytical chemistrySorptionhumic acidSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialsEXAFSColloid and Surface ChemistryAdsorptionchemistryX-ray photoelectron spectroscopyuranium(VI)XPSHumic acidKaoliniteAbsorption (chemistry)surface complexesSpectroscopyJournal of colloid and interface science
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Binding of acrylic and sulphonic polyanions by open-chain polyammonium cations

2000

Abstract The interactions between some acrylic and sulphonic polyanions and some protonated amines (diamines NH 2 -(CH 2 ) x -NH 2 , x =2,…,10; linear tri-, tetra-, penta- and hexa-amines) were studied potentiometrically in aqueous solution, at 25°C. For both types of polyanions AL 2 H i (L − , monomer of polyanion, A, amine) species are formed, with i =1,…, n ( n =number of amino groups in the amine). The stability of these species is strictly dependent on the polyammonium cation charge, and fairly independent of the type of amine (in diamine species maximum stability is observed for x =4, 5). Acrylic and sulphonic polyanion complexes are considerably stronger than analogous species formed…

chemistry.chemical_compoundAqueous solutionChemistryStability constants of complexespolymers; polyamines; polysulphonatesDiaminePolyacrylic acidPolymer chemistryAcid–base titrationAmine gas treatingProtonationPolyelectrolyteAnalytical ChemistryTalanta
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Photoinduced electron transfer in supramolecular complexes of a π-extended viologen with porphyrin monomer and dimer

2012

A π-extended viologen has been synthesized, forming supramolecular complexes with a freebase tetraphenylporphyrin (H2TPP) and the cofacial porphyrin dimer with an anthracene spacer [H4(DPA)] through π–π interaction in benzonitrile (PhCN). Formation of the H2TPP-BHV2+ supramolecular complex was probed by UV-vis and fluorescence spectra. The fluorescence of H2TPP was strongly quenched by electron transfer from the singlet excited state (1H2TPP*) to BHV2+ in the supramolecular complex. The transient absorption spectrum of the charge-separated (CS) state (H2TPP•+ and BHV•+) was successfully detected by the laser flash photolysis measurements of the H2TPP-BHV2+ supramolecular complex in PhCN. Th…

chemistry.chemical_compoundElectron transferBenzonitrilechemistryStability constants of complexesGeneral Chemical EngineeringDimerTetraphenylporphyrinSupramolecular chemistryGeneral ChemistryPhotochemistryPorphyrinPhotoinduced electron transferRSC Advances
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ChemInform Abstract: Ternary Complexes of Cimetidine and Phenobarbital with Cu(II) in Methanolic Solution.

1986

The formation constants of the binary complexes Cu(CM)2+ and Cu(CM) 2 2+ as well as those of the ternary complexes Cu(CM)L + and Cu(CM)2 L + (CM=Cimetidine=N-Cyano-N′-methyl-N″[(5-methyl-1H-imidazol-4-yl)methyltioethyl]-guanidine; HL=Phenobarbital=5-ethyl-5-phenyl-barbituric acid) have been determined in 0.1 and 1.0 mol dm−3 NaClO4 methanol solutions at 25±0.2°C. The values of logX, log βstat.., and Δ logK confirm the stability of the ternary complexes.

chemistry.chemical_compoundchemistryStability constants of complexesInorganic chemistrymedicinePhenobarbitalGeneral MedicineMethanolCimetidineTernary operationmedicine.drugNuclear chemistryChemischer Informationsdienst
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Electrochemical determination of the stability of complexes formed by proton-ionizable ligands of 3,5-disubstituted 1H-pyrazole with phenethylamine

1999

The application of two extreme models for diffusion in two-component systems to electrochemically determine equilibrium constants is discussed. The application of cyclic voltammetric, diferential pulse and rotating-disc electrode voltammetric data to elucidate the stoichiometry and formation constant of complex species by applying a generalization of the molar-ratio method is described. Molar-ratio experiments permit the distinction between the limiting diffusive regimes. The values of the equilibrium stability constants for complexation of phenethylamine and phenethylammonium ions by a 26-membered dioxotetraester crown of 3,5-disubstituted 1H-pyrazole as free ligand 1[L] and as dipyrazolat…

chemistry.chemical_compoundchemistryStability constants of complexesLigandComputational chemistryInorganic chemistryRotating disk electrodePyrazoleElectrochemistryEquilibrium constantAnalytical ChemistryCyclophaneInclusion compoundTalanta
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Ternary complexes of cimetidine and phenobarbital with Cu(II) in methanolic solution

1986

The formation constants of the binary complexes Cu(CM)2+ and Cu(CM) 2 2+ as well as those of the ternary complexes Cu(CM)L + and Cu(CM)2 L + (CM=Cimetidine=N-Cyano-N′-methyl-N″[(5-methyl-1H-imidazol-4-yl)methyltioethyl]-guanidine; HL=Phenobarbital=5-ethyl-5-phenyl-barbituric acid) have been determined in 0.1 and 1.0 mol dm−3 NaClO4 methanol solutions at 25±0.2°C. The values of logX, log βstat.., and Δ logK confirm the stability of the ternary complexes.

chemistry.chemical_compoundchemistryStability constants of complexesmedicinePhenobarbitalGeneral ChemistryMethanolCimetidineTernary operationmedicine.drugNuclear chemistryMonatshefte f�r Chemie Chemical Monthly
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Atrane complexes chemistry as a tool for obtaining trimodal UVM-7-like porous silica

2018

[EN] The use of atrane complexes as hydrolytic precursors enables the homogeneous incorporation of manganese (25Si/Mn48) throughout the porous walls of the nanoparticles of a surfactant-templated bimodal mesoporous silica (UVM-7). The subsequent leaching of the manganese nanodomains allows adding controlled microporosity to the host silica framework. The resulting final silica material presents three pore systems structured at different length scales: interparticle textural-type macroporosity (ca. 43.2nm), ordered intraparticle mesoporosity (ca. 2.63nm; after template removal), and well-dispersed microporosity (< 2nm; as consequence of the lixiviation of the Mn-rich domains). The good dispe…

chemistry.chemical_elementNanoparticle02 engineering and technologyManganeseMesoporous010402 general chemistry01 natural scienceschemistry.chemical_compoundAtrane complexesMaterials ChemistryPhysical and Theoretical ChemistryPorosityChemistryQUIMICA INORGANICASilicaMicroporous materialMesoporous silica021001 nanoscience & nanotechnology0104 chemical sciencesAtraneChemical engineeringEtchingMicroporousLeaching (metallurgy)0210 nano-technologyMesoporous material
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Base-assisted synthesis of 4-pyridinate gold(I) metallaligands: a study of their use in self-assembly reactions

2021

Made available in DSpace on 2021-06-25T12:16:58Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-05-06 Ministerio de Economia y Competitividad (MINECO/FEDER) of Spain Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) The synthesis of di- and tritopic gold(I) metallaligands of the type [(Au4-py)(2)(mu(2)-diphosphane)] (diphosphane = bis(diphenylphosphanyl)isopropane or dppip (1), 1,2-bis(diphenylphosphanyl)ethane or dppe (2), 1,3-bis(diphenylphosphanyl)propane or dppp (3) and 1,4-bis(diphenylphosphanyl)butane or dppb (4)) and [(Au4-py)(3)(mu(3)-triphosphane)] (triphosphane = 1,1,1-tris(diphenylphosph…

chemistry.chemical_elementOrNuclear magnetic resonance spectroscopyLigandsMedicinal chemistryAcceptorComplexos metàl·licsTriphosInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundTriphosphaneLligandschemistryMetal complexesDiphosphaneGoldPlatinumPalladium
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