Search results for "Chela"

showing 10 items of 415 documents

Adduct formation by sub-coordinated metal complexes—VI. Synthesis and pyridine adducts of some nickel(II) chelates formally tri-coordinated

1976

Polymers and Plasticschemistry.chemical_elementAdductMetalchemistry.chemical_compoundNickelchemistryvisual_artPyridinePolymer chemistryMaterials Chemistryvisual_art.visual_art_mediumOrganic chemistryChelationJournal of Inorganic and Nuclear Chemistry
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Antioxidant activity of TunisianGeranium robertianumL. (Geraniaceae)

2013

The present investigation focuses on the methanolic extract obtained from Geranium robertianum L. (Geraniaceae) (Herb Robert), a herbal plant used in traditional medicine for the treatment of human and animal diseases. The antioxidant capacities of the extract were evaluated using 1,1-diphenyl-2- picrylhydrazyl radical, β-carotene/linoleic acid and reducing power and metal chelating activity assays. The amount of total phenolic content, flavonoids and condensed tannins was very high, and the correlation between the antioxidant activity potential and total phenolic level of the extract was pointed out.

PolyphenolMetal chelating activityAntioxidantDPPHGeraniumLinoleic acidmedicine.medical_treatmentMetal chelating activityPlant ScienceBiochemistryAntioxidantsAnalytical Chemistrychemistry.chemical_compoundβ-carotene/linoleic acidAntioxidant activityBotanyGeranium robertianummedicinePlants MedicinalTraditional medicinebiologyPlant ExtractsOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationGeranium robertianum LchemistryProanthocyanidinPolyphenolReducing powerGeraniaceaeDPPHNatural Product Research
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Structural Diversity due to Amino Alcohol Ligands Leading to Rare μ4-Hydroxo-Bridged Tetranuclear and “Bicapped Cubane” Cores in Copper(II) Complexes…

2013

The μ4-hydroxo- and alkoxo-bridged tetranuclear copper(II) complexes, [Cu4(μ4-OH)(dmae)4][Ag(NO3)4] (1), [Cu4(μ4-OH)(dmae)4][Na(NO3)4] (2), [Cu4(μ4-OH)(dmae)4][K(NO3)4] (3), and hexanuclear alkoxo-bridged "bicapped cubane" copper(II) complex [Cu6(ae)8(ClO4)2](ClO4)2·MeOH (8) (dmae = N,N-dimethylaminoethanolato and ae = 2-aminoethanolato) were synthesized via self-assembly from chelating amino alcohols and copper(II), silver (1), sodium (2), and potassium (3) nitrates or copper(II) perchlorate (8). The complexes are characterized by elemental analyses, single-crystal X-ray diffraction, and variable temperature magnetic measurements. The crystal structures of complexes 1-3 consist of almost p…

PotassiumSodiumInorganic chemistryIonic bondingchemistry.chemical_elementCrystal structureCopperInorganic Chemistrychemistry.chemical_compoundPerchlorateCrystallographychemistryCubaneChelationPhysical and Theoretical Chemistryta116Inorganic Chemistry
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Efficient Synthesis of Multifunctional Chelating Agents Based on Tetraazacycloalkanes

2018

An efficient route has been developed for the synthesis of multifunctional tetraazacycloalkanes (in particular 1,4,7,10-tetraazacyclotridecane) incorporating an aminomethyl pendant arm on the carbon skeleton. Starting from the appropriate C-functionalized bisaminal-protected intermediate, the target macrocycles were easily obtained by means of a step-by-step introduction of the desired functional groups onto the free primary amine group, followed by deprotection of the bisaminal intermediates. This straightforward and versatile synthetic approach paves the way for the design of a new family of multifunctional chelators.

Primary (chemistry)010405 organic chemistryLigandChemistryOrganic ChemistryCarbon skeletonRegioselectivity010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesAmine gas treatingChelationPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Chelation of a proton by oxidized diphosphines

2012

Abstract The chelation of a proton by oxidized diphosphines is studied for the first time both experimentally and theoretically. As a proof of concept the rare case where two different H-bond systems exist in one compound, H[7,8-(OP i Pr 2 ) 2 -7,8- nido -C 2 B 9 H 10 ] is reported. Based on NBO, QTAIM and ELF calculations, the P–O⋯H + ⋯O–P interactions were characterized as strong hydrogen bonds.

ProtonHydrogen bondChemistryOrganic ChemistryPhotochemistryBiochemistryMedicinal chemistryInorganic ChemistryDiphosphinesRare caseMaterials ChemistryChelationPhysical and Theoretical Chemistryta116Natural bond orbitalJOURNAL OF ORGANOMETALLLIC CHEMISTRY
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Importance of ligand speciation in environmental research:A case study

2001

The speciations of EDTA and DTPA in process, waste and river waters are modelled and simulated, specifically to the mode of occurrence in the pulp and paper mill effluents and subsequently in receiving waters. Due to relatively short residence times in bleaching process and waste water treatment and slow exchange kinetics, it is expected that the thermodynamic equilibrium is not necessarily reached. Therefore, the initial speciation plays a key role. As such, the simulations have been extended to the process waters of the pulp and paper industry taking into account estimated average conditions. The results reveal that the main species are; Mn and Ca complexes of EDTA and DTPA in pulp mill p…

Pulp millPaperEnvironmental Engineering02 engineering and technology010501 environmental sciencesengineering.materialLigands01 natural sciencesTransition metalMetals Alkaline EarthEnvironmental ChemistryChelationComputer SimulationWaste Management and DisposalEffluentEdetic Acid0105 earth and related environmental sciencesChelating AgentsAlkaline earth metalChemistrybusiness.industryPulp (paper)Environmental engineeringWaterPaper millPentetic Acid021001 nanoscience & nanotechnologyPollution6. Clean waterEnvironmental chemistryChemical IndustryengineeringSewage treatment0210 nano-technologybusinessWater Pollutants ChemicalEnvironmental Monitoring
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Equilibrium, Kinetic and Structural Properties of Gallium(III) and Some Divalent Metal Complexes Formed with the New DATAm and DATA5m Ligands

2017

The development of 68Ge/68Ga generators has made the positron-emitting 68Ga isotope widely accessible and raised interest in new chelate complexes of Ga3+. The hexadentate 1,4-di(acetate)-6-methyl[amino(methyl)acetate]perhydro-1,4-diazepane (DATAm) ligand and its bifunctional analogue, 1,4-di(acetate)-6-pentanoic acid[amino(methyl)acetate]perhydro-1,4-diazepane (DATA5m), rapidly form complexes with 68Ga in high radiochemical yield. The stability constants of DATAm and DATA5m complexes formed with Ga3+, Zn2+, Cu2+, Mn2+ and Ca2+ have been determined by using pH potentiometry, spectrophotometry (Cu2+) and 1H and 71Ga NMR spectroscopy (Ga3+). The stability constants of Ga(DATAm) and Ga(DATA5m)…

Reaction mechanism010405 organic chemistryLigandOrganic ChemistryInorganic chemistrychemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciencesMedicinal chemistryCatalysisDissociation (chemistry)0104 chemical scienceschemistry.chemical_compoundTransmetalationchemistryTermészettudományokChelationGalliumBifunctionalKémiai tudományok
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One-pot direct synthesis for multifunctional ultrasmall hybrid silica nanoparticles

2018

International audience; Ultrasmall silica nanoparticles (NPs), having hydrodynamic diameters under 10 nm are promising inorganic platforms for imaging and therapeutic applications in medicine. Herein is described a new way for synthesizing such kind of NPs in a one-pot scalable protocol. These NPs bear DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid) ligands on their surface that can chelate different metals suitable for a wide variety of biomedical applications. By varying the ratio of the precursors, the hydrodynamic diameters of the particles can be controlled over the range of 3 to 15 nm. The resulting NPs have been characterized extensively by complementary techniques li…

RelaxometryMaterials scienceGadoliniumBiomedical Engineeringchemistry.chemical_elementNanotechnology02 engineering and technology[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryMass spectrometry01 natural scienceschemistry.chemical_compoundDynamic light scattering[CHIM.ANAL]Chemical Sciences/Analytical chemistryDOTA[CHIM]Chemical SciencesGeneral Materials ScienceChelationComputingMilieux_MISCELLANEOUSGeneral ChemistryGeneral Medicine021001 nanoscience & nanotechnology0104 chemical sciences3. Good healthchemistryParticle0210 nano-technologyPhosphorescence
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Efficacy of preheated chelating agents on calcium ion removal from instrumented root canals

2021

Background The heating of chelating agents such as EDTA increases dentin wettability by decreasing surface tension. However, the calcium ion release effect of preheated chelating agents in instrumented root canals has not yet been mentioned. In this study, it was aimed to evaluate the number of calcium ions removed by the pre-heated chelating agents from the root canals. Material and Methods After 51 bovine teeth were instrumented, three of them were separated as negative controls and the remaining teeth were divided into six groups according to the temperature of the solution (at 22 or 37ºC): EDTA-22, CITRIC-22, QMix-22, EDTA-37, CITRIC-37 and QMix-37. Following irrigation, calcium ion lev…

ResearchSignificant differenceSmear layerchemistry.chemical_elementNegative controlCalciumOperative Dentistry and Endodonticslaw.inventionchemistry.chemical_compoundmedicine.anatomical_structurechemistrylawDentinmedicineChelationAtomic absorption spectroscopyCitric acidGeneral DentistryUNESCO:CIENCIAS MÉDICASNuclear chemistryJournal of Clinical and Experimental Dentistry
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Tuning the nuclearity of iron(iii) polynuclear clusters by using tetradentate Schiff-base ligands

2014

Three novel octanuclear, hexanuclear and tetranuclear complexes of high-spin Fe(III) ions were obtained by the reaction of the N,N′-bis-(1R-imidazol-4-ylmethylene)-ethane-1,2-diamine ligand (R = H, CH3) and its derivatives with Fe(ClO4)3·6H2O and KSCN. The tetradentate Schiff-base ligand acts as a bis(bidentate) chelating bridge between two adjacent high-spin Fe(III) centers. The presence of a methyl group in the imidazolyl substituent, the change of counterions or the replacement of imidazole by pyridine has a drastic effect on the nuclearity of the cluster. The magnetic properties of all compounds exhibit antiferromagnetic interactions via μ-oxo or μ-hydroxo pathways in Fe(III) dimers.

Schiff baseDenticityLigandInorganic chemistrySubstituentGeneral ChemistryCatalysischemistry.chemical_compoundCrystallographychemistryPyridineMaterials ChemistryImidazoleChelationMethyl groupNew J. Chem.
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