Search results for "coordination"

showing 10 items of 1282 documents

Ag+ Complexes as Potential Therapeutic Agents in Medicine and Pharmacy

2019

Silver is a non-essential element with promising antimicrobial and anticancer properties. This work is a detailed summary of the newest findings on the bioinorganic chemistry of silver, with a special focus on the applications of Ag+ complexes and nanoparticles. The coordination chemistry of silver is given a reasonable amount of attention, summarizing the most common silver binding sites and giving examples of such binding motifs in biologically important proteins. Possible applications of this metal and its complexes in medicine, particularly as antibacterial and antifungal agents and in cancer therapy, are discussed in detail. The most recent data on silver nanoparticles are also summari…

Antifungalsilver nanoparticlesSilvermedicine.drug_classCancer therapyMetal NanoparticlesNanoparticleAntineoplastic Agents02 engineering and technologyPharmacology010402 general chemistry01 natural sciencesBiochemistrySilver(I) complexesSilver nanoparticleCoordination complexStructure-Activity RelationshipAnti-Infective AgentsCoordination ComplexesDrug DiscoverymedicineHumansAmino Acid SequenceAmino AcidsIonsPharmacologychemistry.chemical_classificationMolecular StructureChemistryOrganic Chemistryantibacterial and anticancer activity of Ag+021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencescysteine and methionine motifsMolecular Medicine0210 nano-technologyProtein BindingCurrent Medicinal Chemistry
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Oxidative stress protection by manganese complexes of tail-tied aza-scorpiand ligands.

2015

The Mn2+ coordination chemistry of double scorpiand ligands in which two polyazacyclophane macrocycles have been connected by pyridine, phenanthroline and bipyridine spacers has been studied by potentiometry, paramagnetic NMR and electrochemistry. All ligands show high stability with Mn2+ and the complexes were formed in a wide pH range. DFT calculations support the structures and coordination geometries derived from the study. A remarkable antioxidant activity was evidenced for these systems by the McCord-Fridovich assay and in Escherichiacoli sodAsodB deficient bacterial cells. The three systems were tested as anti-inflammatory drugs in human macrophages measuring the accumulation of cyto…

AntioxidantStereochemistrymedicine.medical_treatmentPhenanthrolineInorganic chemistrychemistry.chemical_elementManganese010402 general chemistryElectrochemistry01 natural sciencesBiochemistryAntioxidantsCoordination complexInorganic ChemistrySuperoxide dismutasechemistry.chemical_compoundBipyridineBacterial ProteinsCoordination ComplexesCell Line TumorPyridinemedicineEscherichia coliHumanschemistry.chemical_classificationManganesebiology010405 organic chemistryChemistrySuperoxide DismutaseMacrophagesAnti-Inflammatory Agents Non-Steroidal0104 chemical sciencesOxidative Stressbiology.proteinJournal of inorganic biochemistry
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Complex formation of copper( ), nickel( ) and zinc( ) with ethylophosphonoacetohydroxamic acid: solution speciation, synthesis and structural charac…

2019

We present herein the thermodynamic and X-ray characterisation of a novel ethyl phosphonohydroxamic acid-based Cu( ) metallacrown, predominating in solution in a broad pH range.

Aqueous solutionChemistryLigandCoordination polymerIsothermal titration calorimetry02 engineering and technologyGeneral ChemistryCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCatalysis0104 chemical sciencesCrystallographychemistry.chemical_compoundDeprotonationMaterials ChemistryChelation0210 nano-technologyMetallacrown
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INTERACTIONS OF ORGANOTIN(IV) HALIDES WITH REDUCED GLUTATHIONE IN AQUEOUS-SOLUTION

1993

Abstract Glutathione (GSH) is a compound extremely common among many living organisms in which it plays a fundamental role in the processes of detoxification. Also, organotin(IV) derivatives are more and more commonly used in technological processes or as antitumor drugs. So it seemed interesting to investigate the possible interactions between GSH and organotin compounds in water. Particularly, it has been studied because of its role in the organic radicals linked to the tin center on the stoichiometry and the structure of the adducts. Information was obtained following the reaction between Me n SnCl 4-n (n = 1 to 3) and GSH by Mossbauer and NMR spectroscopies on the assumption that change…

Aqueous solutionChemistryRadicalInorganic chemistrychemistry.chemical_elementQuadrupole splittingBiochemistryMedicinal chemistryInorganic ChemistryTrigonal bipyramidal molecular geometryMössbauer spectroscopyProton NMRTinCoordination geometry
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Coordination properties of the ACE inhibitor captopril towards Me2Sn(IV)2+ in aqueous solution, and biological aspects of some dialkyltin(IV) derivat…

2003

Abstract The coordination of Me 2 Sn(IV) 2+ (M) to captopril { N -[( S )-3-mercapto-2-methylpropionyl]- l -proline, H 2 (cap), H 2 L} in aqueous solution was studied by means of potentiometric titration, electrospray mass spectrometry, 1 H-NMR spectroscopy and Mossbauer spectroscopy in the pH range 2–11 ( I =0.1 mol dm −3 NaClO 4 , 298 K). The results obtained with these methods proved that only monomeric complexes are formed in solution. In the acidic pH range, species with a metal-to-ligand ratio of 1:1 exist. The neutral complex ML, similarly to the complex Me 2 Sn(cap) crystallized in the same pH range, adopts a tbp structure with eq S − and ax COO − , while, instead of the coordina…

Aqueous solutionCoordination sphereLigandOrganic ChemistryInorganic chemistryPotentiometric titrationBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundMonomerchemistryAmideMössbauer spectroscopyMaterials ChemistryMoleculePhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Copper(II)-assisted hydrolysis of 2,4,6-tris(2-pyrimidyl)-1,3,5-triazine (tpymt): syntheses, crystal structures and magnetic properties of [Cu(bpcam)…

2005

Abstract The reaction of the 2,4,6-tris(2-pyrimidyl)-1,3,5-triazine (tpymt) ligand with copper(II) perchlorate or sulfate in aqueous solution affords complexes [Cu(bpcam)(H2O)2]ClO4 · 3H2O (1), [Cu(bpcam)(H2O)2][Cu(bpcam)(H2O)(SO4)] · 2H2O (2) and [Cu2(bpcam)2(H2O)2(SO4)] · H2O (3) [bpcam = bis(2-pyrimidylcarbonyl)amidate], whose structures have been determined by single-crystal X-ray diffraction studies. Copper(II) promotes the hydrolysis of tpymt in mild conditions yielding the bpcam group which is present in the structures of 1–3 as a tridentate ligand. The structure of 1 consists of mononuclear [Cu(bpcam)(H2O)2]+ cations, uncoordinated perchlorate anions and water of crystallization. Th…

Aqueous solutionDenticityCoordination sphereChemistrychemistry.chemical_elementCrystal structureCopperSquare pyramidal molecular geometryInorganic ChemistryMetalPerchloratechemistry.chemical_compoundCrystallographyvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryInorganica Chimica Acta
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Phosphine-diène and Salicylamidines ligands : coordination chemistry, catalysis and therapy

2017

The subject of this thesis concerns the development of new ligands, their coordination chemistry, and the synthesis of the corresponding metal complexes for catalysis and therapy.The first part of this work relates to the synthesis of diene-phosphine ligands, their saturated analogs, and the corresponding arene-ruthenium complexes. Arene decoordination allows the formation of a cationic bimetallic complex where the ligand is diène-η4/κ-P coordinated to the ruthenium. These complexes have been applied to atom transfer radical addition (ATRA) of CCl4 to styrene. When harsh reaction conditions are used, the superiority of the “diene” complexes is highlighted comparing to saturated analogs.The …

Arène-ruthéniumCatalyse[CHIM.COOR] Chemical Sciences/Coordination chemistryCatalysisAmidineROPChimie de coordinationDièneCoordination chemistrySchiff baseBase de SchiffArene-rutheniumDieneAza-dipyrromethenePLAThérapie[CHIM.COOR]Chemical Sciences/Coordination chemistryTherapyATRAAza-dipyrrométhènePhosphine
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Aurophilicity as a cofactor in crystal engineering. Dicyanoaurate(I) anion as a building block in a novel Co(II)–Au(I) bimetallic assembly

2002

A 2D grid-shaped cyanide-bridged Co(II)–Au(I) bimetallic coordination polymer, [Co(DMF)2{Au(CN)2}2], has been prepared from the [Au(CN)2]2 building block; sheets associate pair-wise by aurophilic interactions and the compound exhibits zeolite-like properties. Lloret Pastor, Francisco, Francisco.Lloret@uv.es

AurophilicityStereochemistryCoordination polymerZeolite-like propertiesUNESCO::QUÍMICACrystal engineering010402 general chemistryCrystal engineering01 natural sciencesAurophilicity:QUÍMICA [UNESCO]CatalysisCofactorIonchemistry.chemical_compoundMaterials ChemistryBimetallic stripAurophilicity ; Crystal engineering ; Bimetallic ; Zeolite-like propertiesBimetallicbiologyUNESCO::QUÍMICA::Química inorgánica010405 organic chemistryChemistryMetals and AlloysGeneral ChemistryBlock (periodic table):QUÍMICA::Química inorgánica [UNESCO]3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyCeramics and Compositesbiology.protein
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Kinetics of Zn2+ complexation by a ditopic phenanthroline-azamacrocyclic scorpiand-like receptor.

2012

Coordination of Zn(2+) to a ditopic phenanthroline-macrocycle receptor takes place in three steps, the first one being the coordination to the phenanthroline, followed by the slow movement of the metal to the polyamine macrocycle and a final re-arrangement to coordinate the pendent arm.

Aza CompoundsStereochemistryPhenanthrolineKineticsMetals and AlloysGeneral ChemistryHydrogen-Ion ConcentrationCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMetalchemistry.chemical_compoundKineticsZincchemistryCoordination Complexesvisual_artPolymer chemistryMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumSlow MovementPolyamineReceptorPhenanthrolinesChemical communications (Cambridge, England)
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Stepwise formation of a pentanuclear Ni4Cu heterometallic complex exhibiting a vertex-sharing defective double-cubane core and diphenoxo- and phenoxo…

2013

Sequential reaction of a N5O3 octadentate tripodal ligand with Ni(2+) and subsequently with Cu(2+) and azide ligand afforded the first example of a heterobridged (phenoxo/μ(1,1)-azido) pentanuclear heterometallic (Ni4Cu) compound, which exhibits a centrosymmetric vertex-sharing defective double-cubane structure. The study of the magnetic properties reveals that the compound shows ferromagnetic interaction interactions, leading to an S = 9/2 spin ground state. Density functional theory calculations on the X-ray structure and model compounds predict ferromagnetic interactions through the magnetic exchange pathways involving each couple of metal ions.

AzidesMagnetic Resonance SpectroscopyMolecular StructureChemistryStereochemistryMetal ions in aqueous solutionStereoisomerismCrystallography X-RayLigandsVertex (geometry)Inorganic Chemistrychemistry.chemical_compoundCrystallographyFerromagnetismCubaneCoordination ComplexesNickelTripodal ligandQuantum TheoryDensity functional theoryAzidePhysical and Theoretical ChemistryGround stateCopperInorganic chemistry
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