Search results for " complexes"

showing 10 items of 818 documents

Unprecedented reactivity of a Schiff base ligand in the co-ordination sphere of copper(I) complex towards β-diketones. Synthesis and X-ray characteri…

2002

International audience; The reactions of the copper(I) derivative [CuL(THF)(CH3CN)]PF6 (1), in which L is the di-imine/pyridine ligand 2,6-bis[1-(2,6-diisopropylphenylimino)ethyl]pyridine, with different β-diketones (2,4-pentanedione (acacH), 1,3-diphenyl-1,3-propanedione (dbm)) yielded the new Cu(I) salt [CuL′2]PF6 (2) (L′: 2-[acetyl]-6-[1-(2,6-diisopropylphenylimino)ethyl]pyridine). These reactions of β-diketones with a di-imine/pyridine ligand co-ordinated to a Cu(I) centre constitute the first example of a partial hydrolysis of such a Schiff base within the inner sphere of a Cu centre. Compound 2·acaH has been characterised by X-ray crystallography. © 2002 Elsevier Science B.V. All righ…

Schiff base010405 organic chemistryLigandStereochemistrychemistry.chemical_elementCrystal structureSchiff base complexesInner sphere electron transfer010402 general chemistry01 natural sciencesMedicinal chemistryCopper0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryCrystal structuresPyridineMaterials Chemistry[CHIM]Chemical SciencesReactivity (chemistry)Physical and Theoretical ChemistryCopper complexesDerivative (chemistry)Inorganica Chimica Acta
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(S)-2-[(2-Hydroxybenzyl)azaniumyl]-4-(methylsulfanyl)butanoate

2011

The zwitterionic title compound, C12H17NO3S, is a reduced Schiff base derived from (S)-N-(2-hydroxybenzylidene)methionine. An intramolecular interaction between the N—H and carboxylate groups forms a roughly planar (r.m.s. deviation = 0.1405 Å) five-membered ring containing the H(N), N, Cα, C(carboxylate) and O atoms in a pentagonal conformation. In the crystal, a supramolecular triangle-shaped motif is generated by molecules held together by O—H...O and N—H...O hydrogen bonds.

Schiff baseCrystallographyChemistryStereochemistryHydrogen bondGeneral ChemistrySettore CHIM/06 - Chimica OrganicaCondensed Matter PhysicsRing (chemistry)Organic PapersCrystalConformation Crystal structure AMINO COMPLEXES DERIVATIVES LIGANDS ACIDS MODELchemistry.chemical_compoundQD901-999Settore CHIM/03 - Chimica Generale E Inorganicasingle-crystal X-ray studyGeneral Materials Science
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Sequestering ability of polyaminopolycarboxylic ligands towards dioxouranium(VI) cation

2006

Abstract In the present paper, some results of an investigation (at t = 25 °C by potentiometry, ISE-H+ glass electrode) on the sequestering ability of five different polyaminopolycarboxylic ligands [Nitrilotriacetate (NTA), ethylenediamine-N,N,N′,N′-tetraacetate (EDTA), ethylene glycol-bis(2-aminoethylether)-N,N,N′,N′-tetraacetate (EGTA), diethylenetriamine-N,N,N′,N″,N″-pentaacetate (DTPA), triethylenetetraamine-N,N,N′,N″,N′′′,N′′′-hexaacetate (TTHA)] towards dioxouranium(VI) cation in sodium chloride aqueous solutions, at I = 0.7 mol L−1 are reported. Calculations performed on potentiometric data gave evidence of the formation of the following species (log β in parenthesis): UO2(NTA)H0 (12…

Sequestering abilityEthyleneAqueous solutionLigandSpeciationMechanical EngineeringSodiumPotentiometric titrationMetals and Alloyschemistry.chemical_elementDioxouranium(VI); Polyaminopolycarboxylic ligands; Speciation; Sequestering ability; Stability constantsPolyaminopolycarboxylic ligandsDioxouranium(VI)chemistry.chemical_compoundEGTAchemistryMechanics of MaterialsStability constants of complexesMaterials ChemistrySettore CHIM/01 - Chimica AnaliticaChelationPolyaminopolycarboxylic ligandStability constantsNuclear chemistryJournal of Alloys and Compounds
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Weak aurophilic interactions in a series of Au(III) double salts.

2015

In this work, several new examples of rare AuIII⋯AuIII aurophilic contacts are reported. A series of gold(III) double salts and complexes, viz. [AuX2(L)][AuX4] (L = 2,2′-bipyridyl, X = Cl 1, Br 2; L = 2,2′-bipyrimidine, X = Cl 3, Br 4; L = 2,2′-dipyridylamine, X = Cl 5, Br 6), [AuX3(biq)] (biq = 2,2′-biquinoline, X = Cl 7, Br 8), [LH][AuX4] (L = 2,2′-bipyridyl, X = Cl 9; L = 2,2′-bipyrimidine, X = Cl 12; L = 2,2′-dipyridylamine, X = Cl 14, Br 15; L = 2,2′-biquinoline, X = Cl 17, Br 18), [AuBr2(bpy)]2[AuBr4][AuBr2] 10, [AuCl2(bpm)][AuCl2] 11, (bpmH)2[AuBr4][AuBr2] 13, and (dpaH)[AuBr2] 16 (1, 2, and 7 were reported earlier) was synthesized by coordination of a particular ligand to the AuIII …

Series (mathematics)ChemistryLigandAtoms in moleculesstructural dataAurophilicityInorganic ChemistryMetalsymbols.namesakeCrystallographygold complexesComputational chemistryvisual_artDensity analysisvisual_art.visual_art_mediumsymbolsMoleculeVan der Waals radiusgold double saltsta116aurophilic interactionsDalton transactions (Cambridge, England : 2003)
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Melanoma cells release extracellular vesicles which contain RNA-binding proteins able to bind the mRNA encoding histone H1°

2015

Extracellular vesicles (EVs) are produced by most prokaryotic and eukaryotic cells; tumour cells, however, release much higher amounts of EVs, which contain cancer-specific proteins and RNAs. Molecules carried by EVs are captured by surrounding cells, which then undergo profound phenotypic modifications. G26/24 oligodendroglioma cells release, for example, EVs containing FasL and TRAIL, which induce apoptosis in rat cortical neurons and astrocytes in culture. By metabolic labelling of cells, EV-mediated horizontal transfer of radioactive proteins was clearly demonstrated. Among the proteins present in EVs produced by oligodendroglioma cells, extracellular matrix remodelling proteases, and t…

Settore BIO/10 - BiochimicaSettore BIO/06 - Anatomia Comparata E CitologiaExtracellular vesicles (EVs) G26/24 oligodendroglioma cells xtracellular matrix remodelling proteases A375 melanoma cells H1° histone RNA-protein complexes myelin expression factor-2 (MYEF2)
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Kinetic and equilibrium study for Pd(II) removal from aqueous solution by sorption onto calcium alginate gel beads

2013

The more and more increasing use of catalytic converters to reduce the dangerous NOx and CO emission in the atmosphere by vehicle traffic produces a corresponding increase of palladium in the environment [1]. Among the so-called “platinum group Elements” (PGE), elemental palladium seems to be the most hazardous one because it can be easily and quickly oxidized to palladium(II) when put in contact with soil. The presence of palladium oxidized form is of great concern owing to its recognized toxicity towards plants, animals and humans. Therefore, as for the classical “heavy metals”, a removal of this element from the environment is needed and a subsequent recovery for its potential re-use is …

Settore CHIM/01 - Chimica Analiticametal complexes environment biosorption metal removal palladium chemical speciation
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The interaction of DNA with metal complexes: computational investigations

2012

Settore CHIM/03 - Chimica Generale E InorganicaDNA Computational Metal complexesSettore CHIM/08 - Chimica Farmaceutica
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The interaction of native calf thymus DNA with dipyrido[3,2-a;2',3'-c]phenazine and its heteroleptic Iron(III) complexes

2010

Settore CHIM/03 - Chimica Generale E InorganicaIron(III) DNA Intercalators Complexes
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Ni(II) and Zn(II) Schiff Base complexes: B-DNA vs G4-DNA binding

2015

Settore CHIM/03 - Chimica Generale E InorganicaSettore BIO/10 - BiochimicaSettore CHIM/08 - Chimica FarmaceuticaNi(II) Schiff bases Zn(II) Schiff bases complexes with B-DNA complexes with G4-DNA
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Synthesis and chemical characterization of CuII, NiII and ZnII complexes of 3,5-bis(20-pyridyl)-1,2,4-oxadiazole and 3-(20-pyridyl)5-(phenyl)-1,2,4-o…

2011

The synthesis and structural characterization of NiII, CuII and ZnII complexes of two chelating 1,2, 4-oxadiazole ligands, namely 3,5-bis(20-pyridyl)-1,2,4-oxadiazole (bipyOXA) and 3-(20-pyridyl)5- (phenyl)-1,2,4-oxadiazole (pyOXA), is here reported. The formed hexacoordinated metal complexes are [M(bipyOXA)2(H2O)2](ClO4)2 and [M(pyOXA)2(ClO4)2], respectively (M = Ni, Cu, Zn). X-ray crystallography, 1H and 13C NMR spectroscopy and C, N, H elemental analysis data concord in attributing them an octahedral coordination geometry. The two coordinated pyOXA ligands assume a trans coplanar disposition, while the two bipyOXA ligands are not. The latter result is a possible consequence of the format…

Settore CHIM/03 - Chimica Generale E InorganicaSettore CHIM/06 - Chimica OrganicaCopper(II) complexes Crystal structure Nickel(II) complexes 124-Oxadiazoles Zinc(II) complexes
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