Search results for "Complex."

showing 10 items of 5824 documents

Mechanism of anionic polymerization of (meth)acrylates in the presence of aluminium alkyls, 1. 13C NMR studies of model compounds in toluene

1994

The bimetallic ate complex [(CH 3 ) 2 C=C(OEt)(O - AlR 3 )]Li + is regarded to be the model of the active centre of the polymerization of methyl methacrylate in the presence of aluminium alkyls. This complex is detectable by 13 C NMR up to 273 K. At ambient temperature irreversible decomposition takes place. Apart from the formation of the ate complex, excess aluminium chloride coordinates to the ester carbonyl groups of both the monomer and the polymer chain

Aluminium chloridePolymers and PlasticsOrganic Chemistrychemistry.chemical_elementCarbon-13 NMRAte complexchemistry.chemical_compoundMonomerAnionic addition polymerizationchemistryPolymerizationAluminiumPolymer chemistryMaterials ChemistrymedicineMethyl methacrylatemedicine.drugMacromolecular Rapid Communications
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On the formation of inclusion complexes at the solid/liquid interface of anchored temperature-responsive PNIPAAM diblock copolymers with γ-cyclodextr…

2017

The thermal responsive behavior of adsorbed layers of diblock copolymers of poly(N-isopropylacrylamide) (PNIPAAM) and poly((3-acrylamidopropyl)trimethylammonium chloride) (PAMPTMA(+)) with γ-cyclodextrin (γ-CD) at the solid/liquid interface has been investigated using three in situ techniques: null ellipsometry, quartz–crystal microbalance with dissipation monitoring, and neutron reflectometry. The measurements provided information about the adsorbed amounts, the layer thickness, hydration and viscoelastic properties, and the interfacial structure and composition. The copolymers adsorb to silica with the cationic PAMPTMA(+) blocks sitting as anchors in a flat conformation and the PNIPAAM ch…

AmidePolymers and PlasticsBlock copolymerReflectometerReflection02 engineering and technology01 natural sciencessupramolecular chemistryquartz crystal microbalancechemistry.chemical_compoundColloid and Surface ChemistryEllipsometryViscoelasticity Inclusion complexCopolymerMaterials ChemistryPoly (n isopropylacrylamide)Poly(N-isopropylacrylamide)Settore CHIM/02 - Chimica Fisicachemistry.chemical_classification/dk/atira/pure/subjectarea/asjc/1600/1606Reflectometry/dk/atira/pure/subjectarea/asjc/1500/1505Cyclodextrinunclassified drug Article021001 nanoscience & nanotechnologyThermoresponsive block copolymerpriority journalsolidpolymerizationPoly(N-isopropylacrylamide)synthesiNeutron reflectometrypolyrotaxane0210 nano-technologyellipsometryMaterials science/dk/atira/pure/subjectarea/asjc/2500/2505/dk/atira/pure/subjectarea/asjc/2500/2507poly(n isopropylacrylamide)010402 general chemistryLower critical solution temperatureAcrylic monomeratom transfer radical polymerizationAdsorptioncomplex formationPolymer chemistryCyclodextrinliquidPhysical and Theoretical ChemistrySolid/liquid interfaceThermo-responsive Hydrogels copolymerneutron reflectometryInclusion complexgamma cyclodextrinCationic polymerization0104 chemical sciencessolid liquid interfacechemistryChemical engineeringInvited ArticleColloid and Polymer Science
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Synthesis, characterisation and complexation of di- and trifunctional hybrid ferrocenylphosphine ligands.

2020

Organometallic compounds with at least one metal-carbon bond are used in various fields of chemistry: for example, in medical research for anticancer treatments, in catalytic reactions as catalysts or ligands, in electrochemistry for their redox potentials, in materials chemistry for their optical and electronic properties. The principal family of organometallic compounds of this thesis is ferrocene due to its physical and chemical properties particularly its robustness and the possibility of multiple substitutions on cyclopentadienyl ligands, the dissymmetric functionalization of these cyclopentadienyl rings being a major challenge.The first part of this thesis describes the bibliography o…

Aminoacid[CHIM.OTHE] Chemical Sciences/OtherBrönsted acidAcide de BrönstedComplexationFerroceneHybrid ligandLigand hybridePhosphineFerrocèneAminoacide
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New chiral α-aminophosphine oxides and sulfides: an unprecedented rhodium-catalyzed ligand epimerization

2001

International audience; New chiral α-aminophosphine oxide N,P(O) and sulfide N,P(S) ligands have been prepared in one-pot syntheses by addition of Ph2PH to (S)-PhCH[double bond, length half m-dash]NCH(Ph)CH3, followed by oxidation with O2 or S8. Crystallization from cold methanol leads to the isolation of an enantiomerically pure single N,P(O) diastereomer and to a 1 : 1 mixture of the two N,P(S) diastereomers. The coordination chemistry of these ligands with [RhCl(COD)]2 and [RhCl(CO)2]2 has been investigated under argon and syngas. At high temperatures, a P–C oxidative addition of the N,P(O) ligand followed by imine elimination leads to several hydrido rhodium species. The complexes conta…

AminophosphinesIminechemistry.chemical_element010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisCoordination complexRhodiumCatalysischemistry.chemical_compoundEpimerizationMaterials ChemistryOrganic chemistryRhodium[CHIM.COOR]Chemical Sciences/Coordination chemistrychemistry.chemical_classification010405 organic chemistryLigandPhosphine oxides and sulfidesDiastereomerGeneral ChemistryOxidative addition0104 chemical scienceschemistryHydroformylationHydroformylation
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Methods of metal release assessment in soil water at anoxic sites

2006

Department of Geology, Vienna University, Vienna, Austria Metal mobility at contaminated sites can be assessed by soil water investigations or by leaching tests. Leaching tests are usually carried out in open contact with the atmosphere disregarding possible changes of redox conditions. This can affect the original metal speciation and distribution, particularly when anoxic samples are investigated. In this study, the applicability of common leaching tests (the German S4 test (S4), ammonium nitrate extraction (AmmN), and saturation soil extraction (SSE)) is tested for the assessment of zinc release from sulfide-bearing flotation residues of a former ore mine. Results are compared to soil so…

Ammonium nitrateEnvironmental engineeringLessivagechemistry.chemical_elementZincAquatic Sciencecomplex mixturesAnoxic waterschemistry.chemical_compoundchemistryNitrateEnvironmental chemistrySoil waterLeaching (pedology)Environmental ChemistryAmmoniumGeneral Environmental ScienceWater Science and TechnologyActa hydrochimica et hydrobiologica
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Dynamic 2- and 3-connectivity on planar graphs

1992

We study the problem of maintaining the 2-edge-, 2-vertex-, and 3-edge-connected components of a dynamic planar graph subject to edge deletions. The 2-edge-connected components can be maintained in a total of O(n log n) time under any sequence of at most O(n) deletions. This gives O(log n) amortized time per deletion. The 2-vertex- and 3-edge-connected components can be maintained in a total of O(n log2n) time. This gives O(log2n) amortized time per deletion. The space required by all our data structures is O(n).

Amortized analysisBook embeddingPlanar straight-line graph1-planar graphPlanar graphCombinatoricssymbols.namesakePathwidthChordal graphTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYOuterplanar graphData_FILESsymbolsMathematicsofComputing_DISCRETEMATHEMATICSMathematics
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Phylogeography of Ptychadena mascareniensis suggests transoceanic dispersal in a widespread African-Malagasy frog lineage

2004

Aim The Mascarene ridged frog, Ptychadena mascareniensis, is the only African amphibian species thought to occur on Madagascar and on the Seychelles and also Mascarene islands. We explored its phylogenetic relationships and intraspecific genetic differentiation to contribute to the understanding of transoceanic dispersal in amphibians. Methods Fragments of the mitochondrial 16S rRNA gene were sequenced from specimens collected over most of the distribution area of P. mascareniensis, including populations from Madagascar, Mascarenes and Seychelles. Results We identified five deeply divergent clades having pairwise divergences >5%, which probably all represent cryptic species in a P. mascaren…

AmphibianSpecies complexEcologybiologyLineage (evolution)BiogeographyZoologybiology.organism_classificationPhylogeographyPtychadenabiology.animalparasitic diseasesBiological dispersalPtychadena mascareniensisEcology Evolution Behavior and SystematicsJournal of Biogeography
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How self-assembly of amphiphilic molecules can generate complexity in the nanoscale

2015

Abstract Given the importance of nanomaterials and nanostructures in modern technology, in the past decades much effort has been directed to set up efficient bottom up protocols for the piloted self-assembly of molecules. However, molecules are generally disinclined to adopt the desired structural organization because they behave according to their own specific intermolecular interactions. Thus, only some selected classes of chemical compounds are capable to lead to useful self-assembled structures. Amphiphiles, simultaneously possessing polar and apolar moieties within their molecular architecture, can give a wide scenario of possible intermolecular interactions: polar–polar, polar–apolar,…

Amphiphilic moleculeNanostructureStructural organizationChemistryNanomachinesNanotechnologyTop-down and bottom-up designLiving cellComplexitySelf-assemblyNanodevicesNanomachinesSelf-assemblyComplexityNanotechnologyColloid and Surface ChemistryNanotechnologySelf-assemblyNanodevices
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Structural analysis of copper(I) interaction with amyloid β peptide

2019

Abstract The N-terminal fragment of Aβ (β = beta) peptide is able to bind essential transition metal ions like, copper, zinc and iron. Metal binding usually occurs via the imidazole nitrogens of the three His residues which play a key role in the coordination chemistry. Among all the investigated systems, the interaction between copper and Amyloid β assume a biological relevance because of the interplay between the two copper oxidation states, Cu(II) and Cu(I), and their involvement in redox reactions. Both copper ions share the ability to bind Amyloid β. A huge number of investigations have demonstrated that Cu(II) anchors to the N-terminal amino and His6, His13/14 imidazole groups, while …

AmyloidSilverCoordination spherechemistry.chemical_elementPeptide010402 general chemistrySilver(I)01 natural sciencesBiochemistryRedoxCoordination complexInorganic ChemistryMetalchemistry.chemical_compoundCoordination ComplexesImidazoleHistidineAmino Acid SequenceHistidinechemistry.chemical_classificationAmyloid beta-Peptides010405 organic chemistryChemistryStructureCopperPeptide Fragments0104 chemical sciencesCrystallographyCoordinationvisual_artvisual_art.visual_art_mediumCopper(I)CopperProtein BindingJournal of Inorganic Biochemistry
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Requirement for the Proton-Pumping NADH Dehydrogenase I of Escherichia Coli in Respiration of NADH to Fumarate and Its Bioenergetic Implications

1997

In Escherichia coli the expression of the nuo genes encoding the proton pumping NADH dehydrogenase I is stimulated by the presence of fumarate during anaerobic respiration. The regulatory sites required for the induction by fumarate, nitrate and O2 are located at positions around –309, –277, and downstream of –231 bp, respectively, relative to the transcriptional-start site. The fumarate regulator has to be different from the O2 and nitrate regulators ArcA and NarL. For growth by fumarate respiration, the presence of NADH dehydrogenase I was essential, in contrast to aerobic or nitrate respiration which used preferentially NADH dehydrogenase II. The electron transport from NADH to fumarate …

Anaerobic respirationAcetatesmedicine.disease_causeBiochemistryElectron TransportFumaratesEscherichia colimedicineDimethyl SulfoxideNADH NADPH OxidoreductasesAnaerobiosisEscherichia colichemistry.chemical_classificationElectron Transport Complex IEthanolbiologyNADH dehydrogenaseGene Expression Regulation BacterialProton PumpsElectron acceptorFumarate reductaseNADElectron transport chainGlycerol-3-phosphate dehydrogenaseBiochemistrychemistryElectron Transport Complex Ibiology.proteinEnergy MetabolismEuropean Journal of Biochemistry
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