Search results for "ionic"

showing 10 items of 2016 documents

Optical Gating of Photosensitive Synthetic Ion Channels

2011

4-oxo-4-(pyren-4-ylmethoxy) butanoic acid is used as a photolabile protecting group to show the optical gating of nanofluidic devices based on synthetic ion channels. The inner surface of the channels is decorated with monolayers of photolabile hydrophobic molecules that can be removed by irradiation, which leads to the generation of hydrophilic groups. This process can be exploited in the UV-light-triggered permselective transport of ionic species in aqueous solution through the channels. The optical gating of a single conical nanochannel and multichannel polymeric membranes is characterised experimentally and theoretically by means of current-voltage and selective permeation measurements,…

Hydrophilic groupsMaterials scienceSynthetic ion channelsLight sensitive materialsHydrophobicitySynthetic membraneNanotechnologyNano-fluidic devicesGatingIonIonic transportsBiomaterialsPolymeric membranesOptical gatingPhotosensitivityOptical gatingsSynthetic ion channelsMonolayerElectrochemistryControlled releasePhotolabile protecting groupsIonic speciesPolymer membranesHydrophobic moleculesFunctional polymersSelective permeationHydrophilicityMultifunctional devicesMonolayersIonsAqueous solutionCurrent rectificationUV-light irradiationMulti-channelPermeationCondensed Matter PhysicsNanostructuresElectronic Optical and Magnetic MaterialsData processingPhotosensitive nanostructuresFISICA APLICADAIrradiationNano channelsInner surfacesFunctional polymersCurrent voltageAdvanced Functional Materials
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1984

Alkaline hydrolyses of anionic phenyl esters such as 4-acetoxy-3-nitrobenzoic acid and 4-butyryloxy-3-nitrobenzoic acid were examined in the presence of cationic and polymeric liposomes, liposomes of low molecular weight compounds, and micelles. All the additives accelerate the reaction due to the hydrophobic interaction between substrates and additives and the electrostatic interaction both between substrates and additives and between OH− and additives. In the Arrhenius plots of the reactions catalyzed by the liposomes, discontinuous regions were observed due to the phase transition of liposomes from the gel state to the liquid crystal state. Activation parameters ΔH≠, ΔS≠ and ΔV≠ for thes…

Hydrophobic effectLiposomeChemistryPolymer chemistryCationic polymerizationCationic liposomeAlkaline hydrolysis (body disposal)MicellePolyelectrolyteCatalysisDie Makromolekulare Chemie
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Behaviour of Nanomaterials in the Environment: A Study of Interaction between Humic Acids and Fullerene C60

2010

Interaction between buckminsterfullerene and humic substances of different origin was investigated using fluorescence spectrometry as function of concentration of humic substances, pH and ionic strength. Binding constants of humic substances and buckminsterfullerene were calculated. It can be suggested that the complexation was driven by hydrophobic interaction depending on properties of the interacting compounds. Hydrophobic interaction model was indicated by linear Stern–Volmer plot, and high Kd values characterized interaction between buckminsterfullerene and humic acids. The results of this study support the development of understanding of fate of nanomaterials in environment as well as…

Hydrophobic effectchemistry.chemical_compoundBuckminsterfullereneFullerenechemistryIonic strengthInorganic chemistryFluorescence spectrometrycomplex mixturesNanomaterialsLatvian Journal of Chemistry
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Rapid Access to Polyfunctional Lipids with Complex Architecture via Oxyanionic Ring-Opening Polymerization

2011

Polymer-coated liposomes, particularly poly(ethylene glycol) (PEG)-substituted liposomes, have emerged as long-circulating carrier systems for drug delivery and diagnostic purposes. A rapid synthesis of three different types of multifunctional lipids with structurally diverse hydrophilic, polyether-based architectures via one- or two-pot approaches is described. Architectural variation is achieved by the combination of different oxyanionic polymerization strategies and various glycidyl ether building units. Branched polyglycerol lipids have been prepared via cholesterol- or 1,2-bis-n-alkyl glyceryl ether-initiated, oxyanionic ring-opening polymerization (ROP) of protected glycidyl ethers an…

Hyperbranched PolyglycerolsPolymers and PlasticsEffectively ProlongRing-opening polymerizationMicelleCirculation TimeInorganic Chemistrychemistry.chemical_compoundAmphiphilePolymer chemistryMaterials ChemistryCopolymerOrganic chemistryPoly(Ethylene Glycol) CopolymersSolid TumorsCationic-PolymerizationDrug-Delivery SystemsOxide) OligomersEthylene oxideOrganic ChemistryCationic polymerizationEnd-groupchemistryPolymerizationBlock-CopolymersIn-Vivo
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Liquid structure and dynamics in the choline acetate:urea 1:2 deep eutectic solvent

2021

We report on the thermodynamic, structural, and dynamic properties of a recently proposed deep eutectic solvent, formed by choline acetate (ChAc) and urea (U) at the stoichiometric ratio 1:2, hereinafter indicated as ChAc:U. Although the crystalline phase melts at 36-38 degrees C depending on the heating rate, ChAc:U can be easily supercooled at sub-ambient conditions, thus maintaining at the liquid state, with a glass-liquid transition at about -50 degrees C. Synchrotron high energy x-ray scattering experiments provide the experimental data for supporting a reverse Monte Carlo analysis to extract structural information at the atomistic level. This exploration of the liquid structure of ChA…

IONIC LIQUIDMONTE-CARLO CHLORIDE SCATTERING WATER NANOSTRUCTURE NANOSCALEsynchrotron radiationeutecticnuclear relaxationX-ray scatteringhydrogen bondingNMRcholine acetatemolecular dynamicsX-rayMOLECULAR-DYNAMICScholinedeep eutectic solvents X-ray scattering synchrotron radiation NMR nuclear relaxation molecular dynamics choline acetateNUCLEAR-MAGNETIC-RESONANCE MOLECULAR-DYNAMICS IONIC LIQUID SFREE ANALYZER MONTE-CARLO CHLORIDE SCATTERING WATER NANOSTRUCTURE NANOSCALESFREE ANALYZERdeep eutectic solvent thermodynamic properties structural properties dynamic propertiesNUCLEAR-MAGNETIC-RESONANCEdeep eutectic solventsSettore CHIM/02 - Chimica Fisica
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Experimental and theoretical studies on polar Diels–Alder reactions of 1-nitronaphathalene developed in ionic liquids

2013

The reactions between 1-nitronaphthalene 1 and two nucleophilic dienes, Danishefsky´s diene 2 and 1-trimethylsilyloxy-1,3-butadiene 3, to yield phenanthrenols 7 and 8 developed in protic and aprotic ionic liquids (ILs) with an imidazolium cation base permit to conclude that the reactions occur in better experimental conditions than in molecular solvents. The yields obtained with protic ILs are better than those observed with aprotic ILs. In this sense, the higher yields obtained with aprotic ILs, (working at 60ºC, 48 h) are comparable with the lower yields observed in protic ILs (60 ºC, 24 h). DFT calculations for the reaction of 1-nitronaphthalene 1 with diene 3, in the absence and in the …

IONIC LIQUIDTetrafluoroborateDieneGeneral Chemical EngineeringSolvationCiencias QuímicasGeneral ChemistryNitrosoPhotochemistryNITRONAPHTHALENESDFTDIELS-ALDERCatalysischemistry.chemical_compoundQuímica OrgánicachemistryNucleophileComputational chemistryIonic liquidSolvent effectsCIENCIAS NATURALES Y EXACTAS
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Isomer effects in fragmentation of Polycyclic Aromatic Hydrocarbons

2015

We have observed significant differences in the fragmentation patterns of isomeric Polycyclic Aromatic Hydrocarbon (PAH) cations following collisions with helium atoms at center-of-mass energies around 100 eV. This is in contrast to the situation at other collision energies or in photo-absorption experiments where isomeric effects are very weak and where the lowest-energy dissociation channels (H- and C2H2-loss) domihate in statistical fragmentation processes. In the 100 eV range, non-statistical fragmentation also competes and is uniquely linked to losses of single carbon atoms (CHx-losses). We find that such CHx-losses are correlated with the ionic ground state energy within a given group…

IONSCollision-induced dissociationIonic bondingPolycyclic aromatic hydrocarbonPhotochemistryANTHRACENE01 natural sciencesDissociation (chemistry)IsomersMOLECULESchemistry.chemical_compoundFragmentation (mass spectrometry)Fragmentation0103 physical sciencesMoleculeCollisionsTANDEM MASS-SPECTROMETRYPolycyclic Aromatic HydrocarbonsPhysical and Theoretical ChemistryCOLLISION-INDUCED DISSOCIATION010303 astronomy & astrophysicsInstrumentationSpectroscopyNon-statistical fragmentationchemistry.chemical_classificationAnthracenePolycyclic Aromatic Hydrocarbons PAHs[PHYS.PHYS.PHYS-ATM-PH]Physics [physics]/Physics [physics]/Atomic and Molecular Clusters [physics.atm-clus]010401 analytical chemistryCondensed Matter Physics0104 chemical sciencesDIFFERENTIATIONchemistryIONIZATIONCATIONSGROWTH[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Ground stateC14H10International Journal of Mass Spectrometry
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Polymorphism of mytilin B mRNA is not traslated into mature peptide

2008

Diversity of mRNAs from mytilin B, one of the five mytilins identified in the Mediterranean mussel, Mytilus galloprovincialis, has been investigated from circulating hemocytes. One mussel expressed simultaneously two to ten different mytilin B mRNAs as observed in denaturing gradient gel electrophoresis (DGGE), defining 10 individual DGGE patterns (named A to J) within the mussels from Messina, Sicily (Italy). Three patterns accounted for 79% of the individuals whereas other patterns were found in only 2-7% of the 57 analyzed mussels. Base mutations were observed at specific locations, mainly within COOH-terminus and 3'UTR, leading to 36 nucleotide sequence variants and 21 different coding …

ImmunologyMolecular Sequence DataAntimicrobial peptide Defensin mRNA polymorphism DGGE.Evolution MolecularExonchemistry.chemical_compoundOpen Reading FramesAnimalsAmino Acid SequenceRNA MessengerSelection GeneticMolecular BiologyGenePeptide sequencePhylogenyGeneticsElectrophoresis Agar GelMytilusGenomePolymorphism GeneticbiologyBase SequenceMytilinNucleic acid sequenceIntronExonsbiology.organism_classificationMolecular biologyMytiluschemistryGene Expression RegulationProtein BiosynthesisPeptidesTemperature gradient gel electrophoresisAntimicrobial Cationic Peptides
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Novel mixed-valence Cu compounds formed by Cu(II) dimers with double oximato bridges: in situ formation of anionic layer [Cu2(SCN)3]n(n-).

2013

Two new N3O donor ketoxime Schiff bases (HL(1) and HL(2)) have been synthesized by condensing N,N-dimethylethylenediamine with diacetylmonoxime and benzilmonoxime, respectively in a 1:1 ratio. Reaction of Cu(ClO4)2·6H2O with HL(1) resulted in a discrete oximato-bridged dinuclear Cu(II) complex [Cu2(L(1))2(H2O)2](ClO4)2 (1). The same reaction in presence of NaSCN affords the complex {[Cu(II)2(L(1))2][Cu(I)4(μ(1,3)-SCN)4(μ(1,1,3)-SCN)2]}n (2), where partial Cu(II)→Cu(I) reduction is observed. In 2, arrays of [Cu(II)2(L(1))2](2+) cationic units are inserted in between 2D {[Cu(I)4(SCN)6](2-)}n layers and connected via μ(1,1,3)-SCN(-) links, thus forming a 3D network. On the other hand, reaction…

In situAnionsModels MolecularStereochemistryAnionchemistry.chemical_elementInfrared spectroscopy010402 general chemistryCrystallography X-RayAnions; Copper; Crystallography X-Ray; Dimerization; Models Molecular; Molecular Structure; Organometallic Compounds; Oximes; Thiocyanates01 natural sciencesInorganic ChemistryOximeModelsOximes[CHIM.CRIS]Chemical Sciences/CristallographyOrganometallic CompoundsMolecule[CHIM]Chemical SciencesGroup 2 organometallic chemistryOrganometallic CompoundCrystallographyValence (chemistry)Molecular Structure010405 organic chemistryCationic polymerizationMolecular[CHIM.MATE]Chemical Sciences/Material chemistryCopper0104 chemical sciencesCrystallographychemistryX-RaySingle crystalDimerizationCopperThiocyanatesDalton transactions (Cambridge, England : 2003)
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Probing the chemical interaction between iridium nanoparticles and ionic liquid by XPS analysis

2009

Abstract In situ X-ray photoelectron spectroscopy analysis of Ir(0) nanoparticles (1.6 ± 0.3 nm) dispersed in imidazolium ionic liquid (EMI.EtSO4) shows evidences of the effective interaction between the metallic clusters and the surrounding liquid. By monitoring the C 1s signal of the ionic liquid one observes a change of the binding energy in one of its components (C2) when in the presence of Ir nanoparticles. This result was corroborated by isotope labeling experiments.

In situIsotopeBinding energyInorganic chemistryGeneral Physics and AstronomyNanoparticlechemistry.chemical_elementChemical interactionchemistry.chemical_compoundchemistryX-ray photoelectron spectroscopyIonic liquidIridiumPhysical and Theoretical ChemistryChemical Physics Letters
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