Search results for "Carboxylate"

showing 10 items of 640 documents

A solution study of complex formation between iron(III) and oxalate in dimethylsulphoxide

1991

The complex formation between iron(III) and oxalic acid (ethanedioic acid, H2ox) has been studied by potentiometry in dimethylsulphoxide (dmso) solution. H2ox behaves as a weak diprotic acid in such a solvent, with overall association constants: log βj1=8.551(3) and log βj2=14.242(3) at 25°C and 0.1 Mn-Bu4NClO4. A reliable set of overall stability constants for the iron(III)-oxalato complexes, log β11=13.16(4), log β12=23.66(4) and log β13=30.75(4), have been obtained for the first time under identical conditions. The electrochemical behaviour of such complexes was studied in dmso at a platinum electrode. The coordination ability of oxalate towards iron(III) in dmso and water media is compa…

Oxalic acidInorganic chemistryMetals and Alloyschemistry.chemical_elementDiprotic acidOxalateInorganic ChemistrySolventchemistry.chemical_compoundchemistryMaterials ChemistryChemical stabilityCarboxylateCyclic voltammetryPlatinumTransition Metal Chemistry
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Decomposition Process of Carboxylate MOF HKUST-1 Unveiled at the Atomic Scale Level

2016

HKUST-1 is a metal-organic framework (MOF) which plays a significant role both in applicative and basic fields of research, thanks to its outstanding properties of adsorption and catalysis but also because it is a reference material for the study of many general properties of MOFs. Its metallic group comprises a pair of Cu2+ ions chelated by four carboxylate bridges, forming a structure known as paddle-wheel unit, which is the heart of the material. However, previous studies have well established that the paddle-wheel is incline to hydrolysis. In fact, the prolonged exposure of the material to moisture promotes the hydrolysis of Cu-O bonds in the paddle-wheels, so breaking the crystalline n…

metal-organic-frameworks MOF electron paramagnetic resonance EPR ESR water structural stabilityInorganic chemistryFOS: Physical sciences02 engineering and technology010402 general chemistry01 natural sciencesAtomic unitslaw.inventionCatalysisMetalCrystalchemistry.chemical_compoundAdsorptionlawPhysics - Chemical PhysicsCarboxylatePhysical and Theoretical ChemistryElectron paramagnetic resonanceChemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceChemistryMaterials Science (cond-mat.mtrl-sci)021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyChemical engineeringvisual_artvisual_art.visual_art_mediumMetal-organic framework0210 nano-technologyThe Journal of Physical Chemistry C
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Organometallic complexes with biological molecules

2002

Novel triorganotin(IV) complexes of two beta-lactamic antibiotics, 6-[D-(-)-beta-amino-p-hydroxyphenyl-acetamido]penicillin (=amoxicillin) and 6-[D-(-)-alpha-aminobenzyl]penicillin (=ampicillin), have been synthesized and investigated both in solid and solution states. The complexes corresponded to the general formula R(3)Sn(IV)antib*H(2)O (R=Me, n-Bu, Ph; antib=amox=amoxicillinate or amp=ampicillinate). Structural investigations about configuration in the solid state have been carried out by interpreting experimental IR and 119Sn Mossbauer data. In particular, IR results suggested polymeric structures both for R(3)Sn(IV)amox.H(2)O and R(3)Sn(IV)amp*H(2)O. Moreover, both antibiotics appear …

DenticityChemistryStereochemistryNuclear magnetic resonance spectroscopyBiochemistryMedicinal chemistryInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundMoietyMoleculeCarboxylateSolvolysisChromosome breakageJournal of Inorganic Biochemistry
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Microwave-Assisted Synthesis of Polysubstituted 4-Quinolones from Deprotonated α-Aminonitriles

2010

The α-alkylation of deprotonated N-aryl-α-aminonitriles with α-bromoesters furnishes intermediates that can be cyclized to 4-quinolones upon microwave irradiation. Alternatively, base-induced dehydrocyanation of the alkylation products furnishes enaminoesters, which can, for example, be converted into quinoline-3-carboxylates.

chemistry.chemical_compoundDeprotonationMicrowave chemistryChemistryOrganic Chemistry4-quinolonesMicrowave irradiationCarboxylatePhysical and Theoretical ChemistryAlkylationPhotochemistryChemical synthesisMicrowaveEuropean Journal of Organic Chemistry
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Flexible vs Rigid Networks of Two Isoreticular Viologen-Carboxylate based PCPs: the Ligand Size Effect

2018

International audience

LigandChemistryGeneral EngineeringViologen[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry.chemical_compoundPolymer chemistrymedicineGeneral Earth and Planetary Sciences[CHIM]Chemical SciencesCarboxylateComputingMilieux_MISCELLANEOUSGeneral Environmental Sciencemedicine.drug
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Gold nanostars coated with neutral and charged polyethylene glycols: A comparative study of in-vitro biocompatibility and of their interaction with S…

2015

Gold nanostars (GNS) have been coated with four different polyethylene glycols (PEGs) equipped with a -SH function for grafting on the gold surface. These PEGs have different chain lengths with average MW = 2000, 3000, 5000 and average number of -O-CH2-CH2 - units 44, 66, and 111, respectively. Two are neutral and two are terminated with -COOH and -NH2 functions, thus bearing negative and positive charges at physiological pH, thanks to the formation of carboxylate and ammonium groups. The negative charge of the GNS coated with PEG carboxylate has also been exploited to further coat the GNS with the PAH (polyallylamine hydrochloride) cationic polymer. Vitality tests have been carried out on …

Polyethylene glycolBiocompatibilityCell SurvivalMetal NanoparticlesPolyethylene glycolCell morphologyBiochemistryPolyethylene GlycolsInorganic Chemistrychemistry.chemical_compoundNeuroblastomaMicroscopy Electron TransmissionCell Line TumorPEG ratioOrganic chemistryHumansCarboxylatechemistry.chemical_classificationGold nanostarsMolecular StructureEndocytosiCationic polymerizationGold nanostarPolymerEndocytosisTwo-photon luminescenceNanomedicinechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoBiocompatibilityGoldPolyallylamine hydrochlorideNuclear chemistry
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Cycloaddition Reactions with Vinyl Heterocycles

1995

Publisher Summary The Diels-Alder reaction is one of the most common and elegant methods for the construction of six-membered rings. Although the number of Diels-Alder cycloadditions with open-chain and alicyclic dienes is very large, the number of examples with aromatic heterocyclic compounds is relatively small. The introduction of a vinyl group as a substituent onto a heterocycle increases the number of possible reactions. This new possibility, however attractive for synthetic purposes, is successful only with π-excessive five-membered heterocyclic derivatives with a few exceptions. The chapter discusses the reactions of vinyl heterocycles with carbodienophiles. The endocyclic and exo-en…

Dimethyl acetylenedicarboxylatechemistry.chemical_classificationchemistry.chemical_compoundAlicyclic compoundchemistryDienePolymerizationYield (chemistry)SubstituentOrganic chemistrySelectivityCycloaddition
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Interaction of Dimethyltin(IV)2+ Cation with Gly-Gly, Gly-His, and Some Related Ligands. A New Case of a Metal Ion Able To Promote Peptide Nitrogen D…

1999

Equilibrium (pH-metric) and spectroscopic (1H,13C, and 119Sn NMR and 119Sn Mossbauer) studies were performed to characterize the interaction of the dimethyltin(IV) cation with glycine, glycyl-glycine (Gly-Gly), imidazole-4-acetic acid, histamine, histidine, glycyl-histamine, glycyl-histidine (Gly-His), and β-alanyl-histidine (carnosine). For histamine and glycyl-histamine (having only nitrogen donor atoms) no complex formation was detected. The hydrolyzed species of the dimethyltin(IV) cation are always dominant over the complexes formed with the other ligands, except with Gly-Gly and Gly-His. For these two ligands, {COO-,N-,NH2} coordinated complexes are dominant in the neutral pH range wi…

chemistry.chemical_classificationanimal structuresAqueous solutionintegumentary systemInorganic chemistryPeptideMedicinal chemistryInorganic ChemistryMetalchemistry.chemical_compoundTrigonal bipyramidal molecular geometryDeprotonationchemistryvisual_artembryonic structuresvisual_art.visual_art_mediumChelationCarboxylatePhysical and Theoretical ChemistryHistidineInorganic Chemistry
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N-Biphenyl thioureas as carboxylate receptors. Effect of the ligand substituents on the geometry of the complexes

2006

Abstract Six new biphenyl thiourea derivatives have been prepared to be used in carboxylate sensing. Experiments carried out with these ligands have demonstrated that the type of interaction with TBA carboxylates is strongly dependent on the substituents in the thiourea moiety. These interactions go from the formation of 1:1 hydrogen-bonded complexes to acid–base reactions. In addition, different geometries have been observed for the complexes being dependent on the conformations of the free ligands in solution.

Biphenylchemistry.chemical_compoundThioureaChemistryLigandOrganic ChemistryDrug DiscoveryMoietyCarboxylatePhotochemistryReceptorBiochemistryMedicinal chemistryTetrahedron
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Fluorescence of soil humic acids and their fractions obtained by tandem size exclusion chromatography-polyacrylamide gel electrophoresis

2002

Humic acids (HAs) extracted from soils of different origin (chernozem, ferralsol and ranker) and their fractions (A, B and C+D) obtained by tandem size exclusion chromatography–polyacrylamide gel electrophoresis were investigated by steady-state fluorescence spectroscopy in the emission mode. Independently of HA source, high molecular size fractions A and B are shown to be weakly fluorescent. The main fluorophores, especially those emitting at long wavelength (around 500–510 nm), are contained in the polar and low molecular size fractions C+D. As indicated by the observed pH effect, aromatic structures bearing carboxylate and OH substituents may be involved in these longer wavelength emissi…

Gel electrophoresis[SDE] Environmental SciencesChromatographyChemistry[SDV]Life Sciences [q-bio]Size-exclusion chromatographyMineralogyFluorescenceFluorescence spectroscopy[SDV] Life Sciences [q-bio]Electrophoresischemistry.chemical_compoundGeochemistry and Petrology[SDE]Environmental SciencesCarboxylatePolyacrylamide gel electrophoresisChernozem
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