Search results for "ethylenediamine"

showing 10 items of 142 documents

Coordination abilities of l-glutamic acid γ-monohydroxamic acid towards copper(II) in the absence and presence of some aliphatic amines

2012

Abstract Solution equilibrium studies on the Cu 2+ –(A)–(Glu-γ-ha) ternary systems ((A) = polyamine: ethylenediamine (en), diethylenetriamine (dien), N , N , N ′, N ″, N ″-pentamethyldiethylenetriamine (Me 5 dien); (Glu-γ-ha) =  l -glutamic-γ-hydroxamic acid) have been performed by pH-potentiometry, UV–Vis spectrophotometry and EPR methods. The obtained results suggest the formation of the heteroligand complexes with [Cu(A)(Glu-γ-ha)] + stoichiometry in all studied systems. Our spectroscopic results indicate the tetragonal geometry for the [Cu(en)(Glu-γ-ha)] + species in which Glu-γ-ha acts as a tridentate ligand, the geometry slightly deviated from square pyramidal for [Cu(dien)(Glu-γ-ha)]…

Stereochemistrychemistry.chemical_elementEthylenediamineMedicinal chemistryCopperSquare pyramidal molecular geometrylaw.inventionInorganic Chemistrychemistry.chemical_compoundTrigonal bipyramidal molecular geometrychemistrylawDiethylenetriamineMaterials ChemistryPhysical and Theoretical ChemistryElectron paramagnetic resonanceTernary operationStoichiometryInorganica Chimica Acta
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Rate Effects of AOT-Stabilized Microemulsions on Reactions of Ligand Substitution in Cationic Palladium(II) Complexes

1998

Rate data for the substitution reactions of the coordinated ligand X (=2,2‘-bipyridine or 4,4‘-dimethyl-2,2‘-bipyridine) of the palladium(II) complex [Pd(en)X]2+, where en = ethylenediamine, by en or N,N-dimethylethylenediamine in heptane−AOT−water microemulsions have been obtained at 25.0 °C as a function of the AOT concentration at the constant R (=[H2O]/[AOT]) values of 3, 8, and 20 or 30. The overall second-order rate constants are higher in microemulsions than in bulk water and decrease significantly as both the AOT concentration (at constant R) and the molar ratio R (at a given [AOT]) increase. The quantitative analysis of the kinetic data, made by applying the pseudophase model, lead…

Substitution reactionAqueous solutionLigandchemistry.chemical_elementEthylenediamineSurfaces Coatings and Filmschemistry.chemical_compoundReaction rate constantchemistryNucleophileMaterials ChemistryPhysical chemistryOrganic chemistryMicroemulsionPhysical and Theoretical ChemistryPalladiumThe Journal of Physical Chemistry B
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Polymeric drug delivery micelle-like nanocarriers for pulmonary administration of beclomethasone dipropionate

2017

In this paper, the potential of novel polymeric micelles as drug delivery systems for Beclomethasone Dipropionate (BDP) administration into the lung is investigated. These nanostructures are obtained starting from α,β-poly(N-2-hydroxyethyl)-D,L-aspartamide (PHEA), which was subsequently functionalized with O-(2-aminoethyl)-O’-methylpolyethylenglycole (PEG2000), ethylenediamine (EDA) and lipoic acid (LA), obtaining PHEA-PEG2000-EDA-LA graft copolymer. Empty and drug-loaded micelles possess adequate chemical-physical characteristics for pulmonary administration such as spherical shape, slightly positive surface charge and mean size of about 200 nm. Besides, BDP-loaded micelles, obtained …

Surface PropertieAnti-Inflammatory AgentsBiocompatible MaterialsMucin permeation02 engineering and technologyPharmacology030226 pharmacology & pharmacyMicelleAntioxidantsDrug Delivery Systems0302 clinical medicineNanoparticleColloid and Surface ChemistryCopolymerDrug CarrierLungMicellesmedia_commonCell uptakeBiocompatible MaterialDrug CarriersLipoic acidThioctic AcidChemistryBeclomethasoneSurfaces and InterfacesGeneral Medicinerespiratory systemEthylenediamines021001 nanoscience & nanotechnologyPolyaspartamideAnti-Inflammatory AgentDrug deliveryPeptideAntioxidant0210 nano-technologyDrug carrierSurfaces and InterfaceHumanBiotechnologyDrugBiocompatibilitySurface PropertiesCell Survivalmedia_common.quotation_subjectEthylenediamineBronchi03 medical and health sciencesMicroscopy Electron TransmissionPolymeric micelleHumansSurface chargeParticle SizePhysical and Theoretical ChemistryEpithelial CellEthanolEpithelial CellsMicroscopy FluorescenceSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoNanoparticlesNanocarriersPeptidesDrug Delivery SystemNuclear chemistrySustained releaseMicelle
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High-nuclearity Ni-substituted polyoxometalates: a series of poly(polyoxotungstate)s containing 20–22 nickel centers.

2011

Three high-nuclearity Ni-substituted polyoxotungstates (POTs)--[Ni(enMe)2(H2O)2]2[Ni(H2O)6]2[Ni(enMe)2][Ni(H2O)2]1.5[HNi20X4W34(OH)4O136(H2O)6(enMe)8]·11 H2O (3), [Ni(en)2(H2O)]2[H8Ni21X4W34(OH)4O136(en)10(H2O)5]·22 H2O (4), and [Ni(enMe)2]2[H6Ni22X4W34(OH)4O136(H2O)6(enMe)10]·18 H2O (5), in which en = ethylenediamine, enMe = 1,2-diaminopropane, X = 0.5 P+0.5 Ge--were made under hydrothermal conditions and characterized by IR spectroscopy, elemental analysis, thermogravimetric analysis, powder X-ray diffraction, and single-crystal X-ray diffraction. The structures of 3–5 can be viewed as novel derivatives of [H6Ni20P4W34(OH)4O136(enMe)8(H2O)6]·12 H 2O (1) and [Ni(en)2(H2O)]2[H8Ni20P4W34(OH)…

Thermogravimetric analysisMolecular StructureSpectrophotometry InfraredChemistryOrganic ChemistryInorganic chemistryMolecular Conformationchemistry.chemical_elementInfrared spectroscopyEthylenediamineGeneral ChemistryTungsten CompoundsCrystallography X-RayCatalysisNickelchemistry.chemical_compoundCrystallographyNickelPolyoxometalateHydrothermal synthesisMoleculeStructural unitChemistry (Weinheim an der Bergstrasse, Germany)
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Supramolecular diversity and magnetic properties of novel heterometallic Cu(II)/Cr(III) complexes prepared from copper powder, Reineckes salt and eth…

2009

Abstract Three novel heterometallic complexes [Cu(en) 2 Cr(NCS) 4 (NH 3 ) 2 ][Cr(NCS) 4 (NH 3 ) 2 ] · 6dmf ( 1 ), [Cu(en) 2 Cr(NCS) 4 (NH 3 ) 2 ](OAc) ( 2 ) and [{Cu(en) 2 } 3 {Cr(NCS) 4 (NH 3 ) 2 } 2 (NCS) 2 ](NCS) 2 ( 3 ) have been synthesized in a one-pot reaction from copper powder, Reineckes salt, NH 4 X [X −  = OAc − ( 2 ), NCS − ( 3 )] in a dmf ( 1 ) or CH 3 CN ( 2 , 3 ) solution of ethylenediamine (en). X-ray studies showed that 1 and 2 consist of cationic polymeric chains, formed by Cu ( en ) 2 2 + and Cr ( NCS ) 4 ( NH 3 ) 2 - building blocks that bridged through thiocyanate anions. In both complexes, distinct hydrogen bonds are present and serve to increase the dimensionality of …

ThiocyanateHydrogen bondChemistryStereochemistrySupramolecular chemistryCationic polymerizationchemistry.chemical_elementEthylenediamineCopperSupramolecular assemblyInorganic ChemistryCrystallographychemistry.chemical_compoundChromiumMaterials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
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Copper(II) Polyamine Complexes withN-Benzothiazole Sulfonamides as Counterions — Synthesis, Crystal Structures, and Properties of [Cu(dien)2](L1)2[HL…

2003

Copper(II) complexes of new N-benzothiazole sulfonamides (HL1= N-2-(benzothiazole)naphtalensulfonamide and HL2 = N-2-(6-chlorobenzothiazole)toluenesulfonamide) with ethylenediamine (en) and diethylenetriamine (dien) have been synthesized and characterised. The crystal structures of [Cu(dien)2](L1)2 (1) and [Cu(en)2(H2O)2](L2)2 (2) compounds have been determined. The metal centre adopts a “4+2” distorted octahedral environment in both complexes. Unusually, the sulfonamidate anions act as counterions. Spectroscopic properties are in good agreement with the crystal structures. The superoxide dismutase (SOD)-like activity of complex 2 has been tested. Kupfer(II)-Polyamin-Komplexe mit N-Benzothi…

biologyChemistryStereochemistrychemistry.chemical_elementEthylenediamineCrystal structureCopperMedicinal chemistryInorganic ChemistryMetalSuperoxide dismutasechemistry.chemical_compoundBenzothiazoleOctahedronvisual_artDiethylenetriaminevisual_art.visual_art_mediumbiology.proteinZeitschrift für anorganische und allgemeine Chemie
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One-step synthesis of resorcarene dimers composed of two tetra-benzoxazine units

1998

Abstract The condensation of resorcarene 1 with ethylenediamine and an excess of formaldehyde gives, under high dilution conditions, in up to 15% yield the octa-benzoxazine dimer 2 in which two molecules of 1 are connected by four bridges. The structure of 2 has been confirmed by 1 H NMR spectra and MALDI-TOF mass spectra and by hydrolysis of the oxazine rings yielding the secondary amine 3 .

biologyDimerOrganic ChemistryEthylenediamineResorcinarenebiology.organism_classificationBiochemistrychemistry.chemical_compoundchemistryDrug DiscoveryPolymer chemistryMass spectrumProton NMROrganic chemistryTetraMoleculeAmine gas treatingTetrahedron Letters
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CCDC 783768: Experimental Crystal Structure Determination

2011

Related Article: V.Blanco, M.D.Garcia, A.Terenzi, E.Pia, A.Fernandez-Mato, C.Peinador, J.M.Quintela|2010|Chem.-Eur.J.|16|12373|doi:10.1002/chem.201002051

bis(mu~2~-2-(4-(4-pyridylmethyl)phenyl)-27-diazapyrenium)-bis(ethylenediamine)-di-platinum(ii) hexakis(hexafluorophosphate) triphenylene clathrate acetonitrile solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Effect of ethylenediamine on the anodic stripping voltammetric determination of heavy metals in the presence of humic acid

1994

Ligand competition coupled with differential pulse anodic stripping voltammetry has been investigated for the determination of copper, lead and cadmium. Ethylenediamine displaces humic acid in its metal complexes forming kinetically labile compounds. It also eliminates interferences associated with the oxidation of copper. This enhances the sensitivity of the determination of the metals over a wide range of humic acid concentration (up to 30 mg/l). The procedure has been applied to the determination of heavy metals in a real water sample.

chemistry.chemical_classificationCadmiumStripping (chemistry)LigandInorganic chemistrychemistry.chemical_elementEthylenediaminecomplex mixturesBiochemistryCopperAnalytical ChemistryMetalAnodic stripping voltammetrychemistry.chemical_compoundchemistryvisual_artvisual_art.visual_art_mediumHumic acidFresenius' Journal of Analytical Chemistry
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Studien zum Vorgang der Wasserstoffübertragung, 45. Elektroreduktion aromatischer Carbonsäureester

1977

Bei der Elektroreduktion der Benzoesaureester 1 in Alkoholen an einer Quecksilberkathode mit quartare Ammoniumleitsalzen entsteht ein Gemisch von partiell kernhydrierten Reaktionsprodukten und Benzylalkohol (Tabelle 3). Elektroreduziert man jedoch in Gegenwart von Essigsaure, so wird die Kernhydrierung vollstandig unterdruckt und es entstehen ca. 70% Benzylalkohol (3) neben ca. 30% 1,2-Diphenylethylenglykol (9) als Hydrodimerem (Tabelle 4). Benzoesaure-phenylester (2h) wird nahezu ausschlieslich zu Benzylalkohol (3) elektroreduziert; Substituenten an der Benzoesaure (Verbindungen 2a-i) verandern diesen Reaktionsablauf nicht, wenn in Gegenwart von Essigsaure gearbeitet wird (Tabelle 8).Gleic…

chemistry.chemical_classificationCarboxylic acidOrganic ChemistryEthylenediamineAldehydeHydrolysischemistry.chemical_compoundAcetic acidBenzylaminechemistryBenzyl alcoholPolymer chemistryPhysical and Theoretical ChemistryBenzoic acidJustus Liebigs Annalen der Chemie
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