Search results for "ionic"

showing 10 items of 2016 documents

Green conditions for the Suzuki reaction using microwave irradiation and a new HNT- supported ionic liquid-like phase (HNT-SILLP) catalyst

2014

A new catalytic system based on modified halloysite nanotubes was employed in the Suzuki reaction under microwave irradi- ation. A set of solvents, times and bases was screened and the best experimental conditions were obtained when the reactions were carried out for 10 min in water–ethanol at 120 °C in presence of K2CO3 as base. Good recyclability was observed. The new catalytic system was employed using either 1 mol% or 0.1 mol%. The palladium catalyst displayed good activity, allowing the synthesis of several biphenyl compounds in high yield working with only 0.1 mol% palladium loading. The application of mi- crowave irradiation decreased the reaction time and also improved conversion wi…

microwaveSuzuki reactionHalloysite; Suzuki reaction; microwave; SILLP (supported ionic liquid-like phase)HalloysiteSILLP (supported ionic liquid-like phase)Settore CHIM/06 - Chimica OrganicaSettore CHIM/02 - Chimica Fisica
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Micelles in Mixtures of Sodium Dodecyl Sulfate and a Bolaform Surfactant

2006

Mixtures composed of water, sodium dodecyl sulfate (SDS), and a bolaform surfactant with two aza-crown ethers as polar headgroups (termed Bola C-16) were investigated by modulating the mole ratios between the components. The two surfactants have ionic and nonionic, but ionizable, headgroups, respectively. The ionization is due to the complexation of alkali ions by the aza-crown ether unit(s). Structural, thermodynamic, and transport properties of the above mixtures were investigated. Results from surface tension, translational self-diffusion, and small angle neutron scattering ( SANS) are reported and discussed. Interactions between the two surfactants to form mixed micelles result in a com…

mixed micellesIonic bondingEtherANGLE NEUTRON-SCATTERINGMicelleanionic surfactants; mixed micelles; neutron scatteringSurface tensionSurface-Active Agentschemistry.chemical_compoundPulmonary surfactantAQUEOUS-SOLUTIONSSodium sulfateanionic surfactantsElectrochemistrySurface TensionGeneral Materials ScienceSodium dodecyl sulfateSANS surfactant mixtures micellesMicellesSpectroscopyHYDROCARBON SURFACTANTSPHASE SEPARATION MODELChromatographyneutron scatteringSodium Dodecyl SulfateSurfaces and InterfacesCondensed Matter PhysicsSmall-angle neutron scatteringchemistryChemical engineeringLangmuir
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Mūsdienu iespējas tīmekļa un mobilo vairākplatformu lietotņu izstrādē

2020

Pieaug nepieciešamība piedāvāt gan mobilās, gan pārlūka lietotnes, lai nodrošinātu labāku lietotāja pieredzi. Vairākplatformu mobilās izstrādes sistēmas tagad atbalsta arī tīmekļa lietotņu izstrādi kopā ar mobilajām ierīcēm. Darbā, pamatojoties uz dažādiem literāriem avotiem un praktisko pieredzi, tika izpētīti dažādas pieejas un rīki, to iezīmes un izmantošanas potenciāls. No tīmekļa vietņu izstrādes viedokļa tika aprakstītas un apsvērtas vairākplatformu lietotņu grupas. Progresīvās tīmekļa lietotnes, Ionic, NativeScript un Flutter tika salīdzinātas pēc izstrādes procesa, izskata dažādās vidēs, ierīču iespēju piekļuves, pārlūka un operētājsistēmas atbalstu, koda koplietošanas, publicēšanas…

mobilās lietotnesDatorzinātnetīmekļa izstrādevairākplatformu izstrādeFlutterIonic
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Magneto-structural correlations in discrete $Mn^{II}‐W^V$ cyano‐bridged assemblies with polyimine ligands

2010

We present the magneto-structural correlations for two novel discrete cyano-bridged assemblies based on cationic complexes of manganese(II) with diimine ligands and octacyanotungstate(V) ions. The crystal structure of [Mn II (terpy)(dmf)-(H 2 O) 2 ][Mn II (terpy)(H 2 O)(dmf)(μ-NC)W V (CN) 7 ] 2· 6H 2 O (1) (terpy = 2,2';6',2"-terpyridine, dmf = dimethylformamide) contains dinuclear {Mn II W V } - cyano-bridged anions, while the crystal structure of [Mn II (phen) 3 ] 2 [MnII(phen) 2 (μ-NC) 2 -W V (CN) 6 ] 2 (ClO 4 ) 2 ·9H 2 O (2) (phen = 1,10-phenanthroline) is built of tetranuclear {Mn II 2 W V 2} 2- square anions. Intramolecular Mn-W magnetic interactions through the cyano bridges are repr…

molecular squaresStereochemistrytungstenstructure elucidationCationic polymerizationchemistry.chemical_elementcyanidesCrystal structureManganeseIonInorganic Chemistrychemistry.chemical_compoundCrystallographyAtomic orbitalchemistryIntramolecular forcemanganeseDimethylformamidemagnetic propertiesDiimine
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Modelling the dependence on medium and ionic strength of molybdate acidbase properties, and its interactions with phytate

2016

The importance of molybdenum from a biological, environmental and technological point of view is very well known since many decades [15]. In particular, it is mainly present in aqueous solutions as molybdate (MoO42), which is the biologically active form, entering in the cells by active transport systems. Though molybdate is the major species in neutral to basic pH conditions, at lower pH it undergoes protonation and, chiefly, polymerization, even at millimolar concentration levels [2]. Consequently, the modelling of its speciation and acidbase properties is not very simple, as demonstrated by the nonhomogeneity of available literature data. In this light, our group has started a systematic…

molybdatephytateSettore CHIM/01 - Chimica Analiticaacid-base propertieionic strengthionic medium
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STABILITY AND ORGANOCATALYTIC EFFICIENCY OF N-HETEROCYCLIC CARBENES ELECTROGENERATED IN ORGANIC SOLVENTS FROM IMIDAZOLIUM IONIC LIQUIDS

2015

The kinetic of degradation of 1-butyl-3-methylimidazole-2-ylidene (selected as model N-heterocyclic carbene - NHC), generated in organic solvents by cathodic reduction of the parent 1-butyl-3- methylimidazolium salts BMIm-X, was studied by a simple voltammetric analysis. The effect of NHC degradation rate on the efficiency of an organocatalyzed reaction (the synthesis of g-butyrolactone from cinnamaldehyde and trifluoromethylacetophenone) was investigated. The nature of the solvent and of the anion X have a remarkable effect on the stability of the NHC, the bis(trifluoromethylsulfonyl) imide anion being the best for a long lasting carbene (while acetonitrile seems to be the worst solvent). …

n-heterocyclic carbinen-heterocyclic carbeneHydrogen bondanion effect; cyclic voltammetry; ionic liquid; n-heterocyclic carbene; n-heterocyclic carbine; organocatalysisGeneral Chemical EngineeringSettore CHIM/06 - Chimica Organicacyclic voltammetryCinnamaldehydeSolventchemistry.chemical_compoundchemistryOrganocatalysisPolymer chemistryIonic liquidElectrochemistryOrganic chemistryorganocatalysiscyclic voltammetry N-heterocyclic carbene organocatalysis ionic liquid anion effectImideAcetonitrileCarbeneanion effectionic liquid
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Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays.

2017

Three polyaminocyclodextrin materials, obtained by direct reaction between heptakis(6-deoxy-6-iodo)-β-cyclodextrin and the proper linear polyamines, were investigated for their binding properties, in order to assess their potential applications in biological systems, such as vectors for simultaneous drug and gene cellular uptake or alternatively for the protection of macromolecules. In particular, we exploited polarimetry to test their interaction with some model p-nitroaniline derivatives, chosen as probe guests. The data obtained indicate that binding inside the host cavity is mainly affected by interplay between Coulomb interactions and conformational restraints. Moreover, simultaneous i…

nitroanilineaminocyclodextrins; binding properties; nitroanilines; pDNA; polarimetry; supramolecular chemistrySupramolecular chemistryaminocyclodextrins010402 general chemistry01 natural sciencesFull Research Papersupramolecular chemistryaminocyclodextrinlcsh:QD241-441lcsh:Organic chemistrypDNABioassaybinding propertielcsh:Sciencepolarimetry010405 organic chemistryChemistryBinding propertiesOrganic ChemistryCationic polymerizationnitroanilines0104 chemical sciencesChemistrybinding propertiesPolynucleotideBiophysicslcsh:QpUC19Direct reactionMacromoleculeBeilstein journal of organic chemistry
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Generalized Noise Study of Solid-State Nanopores at Low Frequencies.

2017

Nanopore technology has been extensively investigated for analysis of biomolecules, and a success story in this field concerns DNA sequencing using a nanopore chip featuring an array of hundreds of biological nanopores (BioNs). Solid-state nanopores (SSNs) have been explored to attain longer lifetime and higher integration density than what BioNs can offer, but SSNs are generally considered to generate higher noise whose origin remains to be confirmed. Here, we systematically study low-frequency (including thermal and flicker) noise characteristics of SSNs measuring 7 to 200 nm in diameter drilled through a 20-nm-thick SiNx membrane by focused ion milling. Both bulk and surface ionic curren…

noiseta221Analytical chemistryIonic bondingBioengineering02 engineering and technologyElectrolyte010402 general chemistry01 natural sciencesNoise (electronics)Flicker noiseInstrumentationFluid Flow and Transfer Processesta114ChemistryProcess Chemistry and TechnologyFlicker021001 nanoscience & nanotechnology0104 chemical sciencesNanoporenanopore technologyChemical physicssolid-state nanoporesIon milling machine0210 nano-technologyVoltageACS sensors
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Speciation of dimethyltin(IV) – and trimethyltin(IV) – carbocysteinate and – glutamate systems in aqueous media

2008

The formation of complex species in the dimethyltin(IV) and trimethyltin(IV)-carboxymethyl-L-cysteinate (carbocysteinate) systems in NaClaq, at different ionic strengths, and in a multicomponent Na+, K+, Ca2+, Mg2+, Cl- and SO42- medium representative of the seawater major composition, is discussed. Experimental results give evidence for the formation of the following species (L¼carbocysteinate): [(CH3)2Sn(L)]0, [(CH3)2Sn(HL)]+, [(CH3)2Sn(OH)(L)]-, [(CH3)2Sn(OH)2(L)]2- in the DMT–CCYS system, and [(CH3)3Sn(HL)]0, [(CH3)3Sn(L)]- and [(CH3)3Sn(OH)(L)]2- in the TMT-CCYS system. The ionic strength dependence of formation constants was taken into account by an extended Debye Huckel type equation…

organotin(IV) compounds; carboxymethyl-L-cysteinate; glutamateChemical Health and SafetyAqueous mediumChemistrydependence on ionic strength of formation constantHealth Toxicology and Mutagenesismedia_common.quotation_subjectInorganic chemistryComplex formationorganotin(IV) compoundGlutamate receptormixed ionic mediaIonic bondingglutamateToxicologycarboxymethyl-L-cysteinateSpeciationspeciationcomplex formationOrganic chemistrySettore CHIM/01 - Chimica Analiticamedia_commonChemical Speciation & Bioavailability
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Direct P-functionalization of azobenzene by a cationic phosphidozirconocene complex.

2016

International audience; We report that the cationic phosphidozirconocene complex [(eta(5)-C5H5)(2)Zr(PCy2)][CH3B(C6F5)(3)] (II) reacts with azobenzene, resulting in the expedient formation of Zr complex (2) bound to a tridentate PNN ligand. This reaction proceeds by a mechanism of cooperative nucleophilic substitution of hydrogen. The intermediate sigma(H) adduct (1) has been characterized by NMR spectroscopy.

ortho-acylationHydrogenaromatic azo-compoundschemistry.chemical_element[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryBioinformatics01 natural sciences[ CHIM ] Chemical SciencesAdductalcoholsInorganic Chemistrychemistry.chemical_compoundc-h functionalizationPolymer chemistryNucleophilic substitution[CHIM]Chemical Sciences010405 organic chemistryChemistryLigandCationic polymerizationcinnolinium salts[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryNuclear magnetic resonance spectroscopy0104 chemical sciences3. Good healthAzobenzeneazoxybenzenesalpha-oxocarboxylic acidsazoareneshydrogennucleophilic-substitutionSurface modificationDalton transactions (Cambridge, England : 2003)
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