Search results for "Intercalation"

showing 10 items of 126 documents

Fluorescent organometallic rhodium(I) and ruthenium(II) metallodrugs with 4-ethylthio-1,8-naphthalimide ligands: Antiproliferative effects, cellular …

2018

Fluorescent 4-ethylthio-1,8-naphthalimides containing rhodium(I) N-heterocyclic carbene (NHC) and ruthenium (II) NHC fragments were synthesised and evaluated for their antiproliferative effects, cellular uptake and DNA-binding activity. Both types of organometallics triggered ligand dependent efficient cytotoxic effects against tumor cells with the rhodium(I) NHC derivatives causing stronger effects than the ruthenium (II) NHC analogues. Antiproliferative effects could also be observed against several pathogenic Gram-positive bacterial strains, whereas the growth of Gram-negative bacteria was not substantially affected. Cellular uptake was confirmed by atomic absorption spectroscopy as well…

Intercalation (chemistry)Fluorescent DyeLigands01 natural sciencesAntineoplastic Agentchemistry.chemical_compoundNeoplasmsDrug DiscoveryMoietyCell DeathBacterial InfectionsGeneral MedicineIntercalating AgentsNaphthalimideAnti-Bacterial AgentsRutheniumNaphthalimidesSettore CHIM/03 - Chimica Generale E InorganicaHumanStereochemistrychemistry.chemical_elementAntineoplastic AgentsLigandCarbene010402 general chemistryG-quadruplexBacterial InfectionRutheniumRhodiumCell Line TumorAnti-Bacterial AgentOrganometallic CompoundsG-QuadruplexeHumansRhodiumBioorganometallicFluorescent DyesGroup 2 organometallic chemistryCell ProliferationPharmacologyOrganometallic CompoundBacteria010405 organic chemistryLigandOrganic ChemistryIntercalating Agent0104 chemical sciencesG-QuadruplexeschemistryNeoplasmDrug Screening Assays AntitumorCarbene
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Quantifying the Covalent Functionalization of Black Phosphorus

2020

Abstract A straightforward quantification method to consistently determine the overall functionalization degree of covalently modified two‐dimensional (2D) black phosphorus (BP) by Raman spectroscopy has been carried out. Indeed, the successful reductive methylation of the BP lattice using sodium intercalation compounds and exhibiting different functionalization degrees has been demonstrated by 31P‐magic angle spinning (MAS) NMR spectroscopy. Furthermore, the correlation of 31P‐MAS NMR spectroscopy and statistical Raman spectroscopy (SRS) revealed the first method to determine the functionalization degree of BP solely by evaluating the intensities of distinct peaks in the Raman spectra of t…

Intercalation (chemistry)reduction010402 general chemistry01 natural sciencesCatalysisBlack phosphoruslaw.inventionCovalent functionalizationsymbols.namesakelawMaterialsResearch Articles010405 organic chemistryGrapheneChemistryGeneral ChemistryNuclear magnetic resonance spectroscopy3. Good health0104 chemical sciencesEspectroscòpia Ramancovalent functionalizationCovalent bondBlack PhosphorusRaman spectroscopyddc:540symbolsSurface modificationPhysical chemistryRaman spectroscopyResearch Article31P-MAS NMR spectroscopy
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Intercalation of [M(ox)3]3− (M=Cr, Rh) complexes into NiIIFeIII-LDH

2010

Abstract Layered Double Hydroxides (LDH) containing paramagnetic NiII and FeIII ions in the hydroxide layers and chromium or rhodium oxalate complexes at the interlayer space were prepared by ion exchange from a NiFe-LDH precursor with sebacate anions between the hydroxide layers. The precursor was synthesized by coprecipitation at controlled pH in order to avoid the formation of solid phases different from LDH. Magnetic studies demonstrated that both LDHs, NiFe–Cr(ox)3 and NiFe–Rh(ox)3, exhibited a behaviour similar to the precursor. Nevertheless, the substitution of intercalated sebacate anions with oxalate complexes compresses the LDH basal spacing, increasing the intensity of dipolar in…

Ion exchangeCoprecipitationIntercalation (chemistry)Inorganic chemistryLayered double hydroxidesGeologyengineering.materialOxalatechemistry.chemical_compoundParamagnetismchemistryGeochemistry and PetrologyengineeringHydroxideHybrid materialApplied Clay Science
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Intercalation of cobalt(II)-tetraphenylporphine tetrasulfonate complex in magnetic NiFe-layered double hydroxide

2013

Abstract Hybrid magnetic multilayers have been synthesized by means of intercalation of [5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrinato]cobalt(II) (CoTPPS) complex in the interlayer space of a Ni II Fe III layered double hydroxide (LDH), through anion-exchange reaction. A sebacate ( − OOC–(CH 2 ) 8 –COO − ) intercalated NiFe-LDH have been used as precursor, facilitating the anion exchange reaction, thus permitting the inclusion of a paramagnetic macrocycle inside the ferrimagnetic NiFe-LDH layers. The material has been characterized by XRD, FT-IR, SEM, SQUID and ESR. The T c for the hybrid NiFe–CoTPPS, ca. 11–12 K, is very close to that shown by the precursor, despite that the intercala…

Ion exchangeInorganic chemistryIntercalation (chemistry)chemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionInorganic ChemistrySQUIDCrystallographychemistry.chemical_compoundParamagnetismchemistrylawFerrimagnetismMaterials ChemistryHydroxidePhysical and Theoretical Chemistry0210 nano-technologyCobaltPolyhedron
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EXAFS study of hydrogen intercalation into ReO 3 using the evolutionary algorithm.

2014

In this study we have investigated the influence of hydrogen intercalation on the local atomic structure of rhenium trioxide using a new approach to EXAFS data analysis, based on the evolutionary algorithm (EA). The proposed EA-EXAFS method is an extension of the conventional reverse Monte Carlo approach but is computationally more efficient. It allows one to perform accurate analysis of EXAFS data from distant coordination shells, taking into account both multiple-scattering and disorder (thermal and static) effects. The power of the EA-EXAFS method is first demonstrated on an example of the model system, pure ReO3, and then it is applied to an in situ study of hydrogen bronze HxReO3 upon …

Lattice dynamicsExtended X-ray absorption fine structureHydrogenIntercalation (chemistry)Analytical chemistryEvolutionary algorithmchemistry.chemical_elementReverse Monte CarloCondensed Matter PhysicsCondensed Matter::Materials Sciencechemistry.chemical_compoundRhenium trioxidechemistryChemical physicsCondensed Matter::SuperconductivityThermalGeneral Materials ScienceJournal of physics. Condensed matter : an Institute of Physics journal
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Stimuli-responsive hybrid materials: breathing in magnetic layered double hydroxides induced by a thermoresponsive molecule

2014

[EN] A hybrid magnetic multilayer material of micrometric size, with highly crystalline hexagonal crystals consisting of CoAl-LDH ferromagnetic layers intercalated with thermoresponsive 4-(4-anilinophenylazo)benzenesulfonate (AO5) molecules diluted (ratio 9 : 1) with a flexible sodium dodecylsulphate (SDS) surfactant has been obtained. The resulting material exhibits thermochromism attributable to the isomerization between the azo (prevalent at room temperature) and the hydrazone (favoured at higher temperatures) tautomers, leading to a thermomechanical response. In fact, these crystals exhibited thermally induced motion triggering remarkable changes in the crystal morphology and volume. In…

Magnetic couplingsMagnetismLayered double hydroxidesFerromagnetic layersINTERCALATION COMPOUNDengineering.materialThermotropismNI-ALQuantitative Biology::Subcellular ProcessesCondensed Matter::Materials ScienceMETAL-ORGANIC FRAMEWORKSchemistry.chemical_compoundCrystallinityQUIMICA ORGANICANuclear magnetic resonanceCrystal morphologiesPHOTOISOMERIZATIONQUIMICA ANALITICANANOPARTICLESPhysics::Chemical PhysicsAZOBENZENEPhysics::Atmospheric and Oceanic PhysicsThermochromismPRUSSIAN BLUEChemistryMagnetismLayered double hydroxidesFísicaQuímicaGeneral ChemistryMoleculesequipment and suppliesChemistryMagnetic multilayersCrystallographyAzobenzeneFerromagnetismHYDROTALCITEengineeringTHERMAL-EXPANSIONHybrid materialhuman activitiesCOORDINATION POLYMERSChemical Science
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The interaction of Fe(III), adriamycin and daunomycin with nucleotides and DNA and their effects on cell growth of fibroblasts (NIH-3T3)

1996

The interactions of the iron complexes of the anthracycline antitumour drugs daunomycin (DN) and adriamycin (ADM) with the mononucleotide AMP, herring sperm DNA, plasmic pBR322 and immortalized 3T3 fibroblasts were studied. By means of Mössbauer spectroscopy it was demonstrated that DNA is a powerful ferric iron chelator as compared with AMP, which is not able to compete with DN or acetohydroxamic acid for ferric iron. The difference between AMP and DNA is postulated to be based on the chelate effect. The Mössbauer spectra of the ternary Fe-anthracycline-DNA systems differ from Fe-anthracycline binary complexes, indicating rearrangement reactions. Dialysis experiments clearly disclose the f…

MaleBase pairStereochemistryIronIntercalation (chemistry)General Biochemistry Genetics and Molecular BiologyBiomaterialsMiceSpectroscopy Mossbauerchemistry.chemical_compoundmedicineAnimalsNucleotideCytotoxicitychemistry.chemical_classificationChemistryCell growthAcetohydroxamic acidDaunorubicinFishesMetals and AlloysBiological Transport3T3 CellsDNASpermatozoaAdenosine MonophosphateDoxorubicinFerricGeneral Agricultural and Biological SciencesCell DivisionDNAPlasmidsmedicine.drugBiometals
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Influence of Iron Sulfide Nanoparticle Sizes in Solid‐State Batteries**

2021

Abstract Given the inherent performance limitations of intercalation‐based lithium‐ion batteries, solid‐state conversion batteries are promising systems for future energy storage. A high specific capacity and natural abundancy make iron disulfide (FeS2) a promising cathode‐active material. In this work, FeS2 nanoparticles were prepared solvothermally. By adjusting the synthesis conditions, samples with average particle diameters between 10 nm and 35 nm were synthesized. The electrochemical performance was evaluated in solid‐state cells with a Li‐argyrodite solid electrolyte. While the reduction of FeS2 was found to be irreversible in the initial discharge, a stable cycling of the reduced sp…

Materials scienceCommunicationIntercalation (chemistry)NanoparticleIron sulfideconversion electrodesGeneral ChemistryElectrolyteGeneral MedicineSolid‐State BatteriesElectrochemistryCatalysisEnergy storageCommunicationschemistry.chemical_compoundChemical engineeringchemistryElectrodeddc:540ddc:660Particlesolid-state batteriesnanoparticlesiron sulfideAngewandte Chemie
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Molecular dynamics of carrageenan composites reinforced with Cloisite Na+ montmorillonite nanoclay

2017

[EN] Nanocomposites comprising biodegradable carrageenan and glycerol(KCg) as the host polymer, with different contents of natural montmorillonite (MMT) as filler, were prepared by a solution casting process. Different techniques have been used to determine the interaction/behavior among the different components of the samples such as Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Transmission electron microscope (TEM) and, mainly, Dielectric relaxation spectroscopy (DRS). FTIR indicates hydrogen interaction between carrageenan matrix and silicate that is confirmed by the XRD data indicating some kind of carrageenan intercalation between the MMT layers. A rather ho…

Materials scienceElectric modulusPolymers and PlasticsIntercalation (chemistry)02 engineering and technologyActivation energyDielectric relaxation spectroscopy010402 general chemistryCarrageenan01 natural scienceschemistry.chemical_compoundMaterials ChemistryFragilityFourier transform infrared spectroscopyComposite materialchemistry.chemical_classificationNanocompositeOrganic ChemistryRelaxation (NMR)Polymer021001 nanoscience & nanotechnology0104 chemical sciencesMontmorillonitechemistryMAQUINAS Y MOTORES TERMICOS0210 nano-technologyGlass transitionTERMODINAMICA APLICADA (UPV)
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Electrochemical Fabrication and Physicochemical Characterization of Metal/High-k Insulating Oxide/Polymer/Electrolyte Junctions

2014

Photoelectrochemical polymerization of poly(3,4-ethylenedioxythiophene), PEDOT, was successfully realized on anodic film grown to 50 V on magnetron sputtered Ti-6 atom % Si alloys. Scanning electron microscopy allowed us to evidence formation of compact and uniform polymer layers on the oxide surface. Photoelectrochemical and impedance measurements showed that photopolymerization allows one to grow PEDOT in its conducting state, while a strong cathodic polarization is necessary to bring the polymer in its p-type semiconducting state. Information on the optical and electrical properties of metal/oxide/polymer/electrolyte junctions proves that PEDOT has promising performance as an electrolyte…

Materials scienceFabricationElectrochemical fabricationInorganic chemistryImpedance measurementOxidePhysico-chemical characterizationPoly-3 4-ethylenedioxythiopheneElectrolyteElectrochemistrySettore ING-INF/01 - ElettronicaPhotoelectrochemistrychemistry.chemical_compoundPEDOT:PSSPhysical and Theoretical ChemistryConducting statechemistry.chemical_classificationPhotopolymerizationCathodic polarizationPolymerSilicon alloySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOptical and electrical propertieSettore ING-IND/23 - Chimica Fisica ApplicataGeneral EnergychemistryPolymerizationCavity magnetronLithium IntercalationTitanium alloyScanning electron microscopyThe Journal of Physical Chemistry C
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