Search results for "ionic"

showing 10 items of 2016 documents

Crystal structure of cis-bis­(μ-β-alanine-κ2 O:O′)bis[tri­chlorido­rhenium(III)](Re–Re) sesquihydrate

2015

A dirhenium(III) cis-di­carboxyl­ate complex is reported, which is representative of a small class of zwitterionic ammonia­carboxyl­ato complexes involving a quadruple metal–metal bond.

crystal structurechemistry.chemical_elementCrystal structurerheniumChlorideIonResearch CommunicationsCrystallcsh:Chemistryquadruple metal–metal bondmedicineMoleculeGeneral Materials ScienceclusterAlanineLigandGeneral ChemistryRheniumCondensed Matter PhysicsCrystallographychemistrylcsh:QD1-999β-alaninezwitterionic ammonia­carboxyl­ato complexzwitterionic ammoniacarboxylato complexmedicine.drugActa Crystallographica Section E: Crystallographic Communications
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Poly[1-ethyl-3-methylimidazolium [tri-μ-isothiocyanato-manganate(II)]]

2019

The title compound, {(C9H11N2)[Mn(NCS)3]} n , has been obtained as a side product of the salt metathesis reaction of 1-ethyl-3-methylimidazolium bromide, (EMIm)Br, and K2[Mn(NCS)4]. The structure consists of discrete 1-ethyl-3-methylimidazolium cations and an anionic two-dimensional network of manganese(II)-based complex anions, interconnected by thiocyanate ions. Every Mn2+ ion is coordinated by three S atoms of three NCS− ions and three N atoms of further three NCS− ions in a meridional octahedral fashion.

crystal structurethiocyanateThiocyanateManganatechemistry.chemical_elementThio-02 engineering and technologyCrystal structureManganese010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMedicinal chemistry0104 chemical scienceschemistry.chemical_compoundnetwork structurechemistryBromideIonic liquidmanganeselcsh:QD901-999Salt metathesis reactionlcsh:Crystallography0210 nano-technologyionic liquidIUCrData
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Synthesis, characterization and magnetic study of two new octahedral iron(III) complexes with pendant zwitterionic Schiff bases

2016

Two Schiff bases, HL1 [2-((3-(dimethylamino)propylimino)methyl)-5-bromophenol] and HL2 [2-((2-(diethylamino)ethylimino)methyl)-6-methoxyphenol], have been employed to prepare two new octahedral iron(III) complexes, [Fe(HL1)2(N3)2]ClO4·2H2O (1) and [Fe(HL2)2(NCS)2]ClO4·H2O (2). Both complexes are characterized by spectral and elemental analyses. Single crystal X-ray diffraction studies confirm their structures. In both complexes, Schiff bases are trapped in their zwitterionic forms and coordinated to iron(III) only through the imine nitrogen and phenoxo oxygen, i.e., they behave as bi-dentate ligands, keeping the remaining potential donor sites pendant. The measurement of χM vs. T for both c…

crystal structurevariable temperature magnetic susceptibilityIminechemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesOxygenzwiterionicInorganic Chemistrypendantchemistry.chemical_compoundMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryMagnetic studyta116010405 organic chemistryNitrogen0104 chemical sciencesCrystallographychemistryOctahedronPotential donorSingle crystaliron(III)Inorganica Chimica Acta
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Liquid structure of a choline chloride-water natural deep eutectic solvent: A molecular dynamics characterization

2021

The liquid structure of a representative of the first water-in-salt (WiS) Natural Deep Eutectic Solvents (NADES), hereinafter indicated as aquoline, a mixture of choline chloride (ChCl) and water with molar ratio 1:3.33, is ex- plored at ambient conditions. Using Molecular Dynamics (MD) simulation tools, we extract structural informa- tion at atomistic level on the nature of inter-correlations between the different moieties. Despite being a very fluid liquid, with much lower viscosity than other common ChCl-based DES, aquoline turns out to be very struc- tured. Computed X-ray and neutron weighted scattering patterns (the latter also on selectively deuterated mix- tures) highlight the existe…

deep eutectic solvent02 engineering and technology010402 general chemistry01 natural sciencesChloridechemistry.chemical_compoundMolecular dynamicsPhase (matter)Materials ChemistrymedicineMoleculePhysical and Theoretical ChemistrySpectroscopyEutectic systemChemistryHydrogen bond021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and Opticsmolecular dynamicsPARTICLE MESH EWALDIONIC LIQUIDSNEUTRON-SCATTERINGMIXTURESNANOSTRUCTUREDENSITYACID0104 chemical sciencesElectronic Optical and Magnetic MaterialsDeep eutectic solventPhysical chemistry0210 nano-technologyliquid structuremedicine.drugCholine chloride
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Non-stoichiometric dicationic organic salts form supramolecular gels

dicationic organic salts ionogels ionic liquidsSettore CHIM/06 - Chimica Organica
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Ab initio calculations of Nb doped SrTiO3

2010

We present and discuss the results of the large scale Hartree–Fock calculations of Nb impurities substituting for Ti ions in SrTiO3 using ab initio computer code CRYSTAL and several supercells containing up to 135 atoms. The local structure optimisation, the electronic charge redistribution, chemical bond covalence and the band-structure changes induced by the defect are analysed. According to the results of our calculations, Nb is a shallow donor; six nearest O ions are slightly displaced outwards from the Nb ion. The calculated bond population between nearest Ti and O ions (64 me) is much larger than that between Nb and O ions (8 me), since Nb impurity is more ionic than the host Ti.

education.field_of_studyMaterials sciencePopulationAb initioIonic bondingCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsIonCondensed Matter::Materials ScienceChemical bondImpurityAb initio quantum chemistry methodsPhysical chemistryElectrical and Electronic EngineeringAtomic physicseducationShallow donorPhysica B: Condensed Matter
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Gas phase behavior of radical cations of perfluoroalkyl-1,2,4-triazines: an experimental and theoretical study

2009

Electron ionization mass spectrometry and low-energy collision-induced decomposition reactions occurring in a tridimensional ion trap, together with density functional theory (DFT) calculations on neutrals, even- and odd-electron cations, have been used to study the gas-phase ion chemistry of a series of perfluoroalkyl-1,2,4-triazines. Loss of oxygen, due to thermal degradation occurring before ionization, likely involving the hydroxylamino group, has been observed. Compounds having a carbonyl group at position 6 of the triazine ring fragment in the source by elimination of NO followed by HF or CO. The decomposition pathways occurring due to CID experiments have shown interesting features d…

electron ionizationFree RadicalsStereochemistryIonic bondingDFT calculationAntineoplastic AgentsMass spectrometryGas Chromatography-Mass SpectrometryIonradical ionTandem Mass SpectrometryComputational chemistrySpectroscopyElectron ionizationFluorocarbonsMolecular StructureTriazinesChemistryPolyatomic ionSettore CHIM/06 - Chimica OrganicaModels ChemicalRadical ionUnpaired electronDensity functional theorytriazineGasesfluorinated compounds
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Migranti. L'emigrazione ionico etnea: un'esperienza di laboratorio storico.

2006

Si tratta dell'introduzione al volume che indica la metodologia di ricerca trasmessa agli autori delle ricerche

emigrazione ionico etneaSettore SPS/06 - Storia Delle Relazioni Internazionali
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Gene delivery agents possessing antiradical activity: self-assembling cationic amphiphilic 1,4-dihydropyridine derivatives

2013

Seventeen 1,4-dihydropyridine (1,4-DHP) amphiphiles including differently substituted pyridinium, pyrazinium, N-methyl piperidinium or N-methyl morpholinium moieties as the cationic head-group of the molecule have been designed and synthesised. 1,4-DHP amphiphiles have been earlier proposed as a promising tool for plasmid DNA (pDNA) delivery in vitro. In this work the ability of the 1,4-DHP amphiphiles to self-assemble, to bind pDNA and to transfer it into the cells as well as the cytotoxicity of 1,4-DHP amphiphiles–pDNA complexes was studied. Furthermore, antiradical activity (ARA) of the 1,4-DHP derivatives was determined. We have revealed that all new 1,4-DHP amphiphiles possessed self-a…

endocrine systemAqueous solution010405 organic chemistryStereochemistrySubstituentCationic polymerizationGeneral ChemistryGene delivery010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryAmphiphileMaterials ChemistryMoleculePyridiniumCytotoxicityNew Journal of Chemistry
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Electrostatically Driven Complexation of Liposomes with a Star-Shaped Polyelectrolyte to Low-Toxicity Multi-Liposomal Assemblies

2013

Anionic liposomes are electrostatically complexed to a star-shaped cationic polyelectrolyte. Upon complexation, the liposomes retain their integrity and the resulting liposome-star complexes do not dissociate in a physiological solution with 0.15 M NaCl. This provides a multi-liposomal container for possible use as a high-capacity carrier.

endocrine systemLiposomePolymers and PlasticsLow toxicityChemistryCationic polymerizationBioengineeringPolyelectrolyteBiomaterialsStar polymerChemical engineeringMaterials ChemistryOrganic chemistryBiotechnologyMacromolecular Bioscience
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