Search results for "Intercalation"

showing 10 items of 126 documents

DNA interaction of CuII, NiII and ZnII functionalized salphen complexes: studies by linear dichroism, gel electrophoresis and PCR.

2013

The interaction of salphen-type NiII, CuII and ZnII complexes with native DNA was investigated by exploiting linear dichroism experiments. The NiII complex behaves as a typical intercalator, binding strongly and stiffening and unwinding the DNA. The strength of the DNA interaction is slightly weaker for the copper complex and much weaker for the zinc complex. Plasmid-DNA gel electrophoresis experiments indicated that while CuII and ZnII complexes do not induce the unwinding of supercoiled DNA, the NiII complex has a nuclease activity without the addition of external agents. On the other hand, as shown in the PCR assays, we demonstrate that, at the used concentrations, only the CuII complex …

StereochemistryIntercalation (chemistry)Molecular Conformationchemistry.chemical_elementZincPhenylenediaminesLinear dichroismCrystallography X-RayPolymerase Chain ReactionInorganic Chemistrychemistry.chemical_compoundBiomimetic MaterialsCoordination ComplexesNickelGel electrophoresisElectrophoresis Agar GelNucleaseDeoxyribonucleasesbiologyCircular DichroismDNASettore CHIM/08 - Chimica FarmaceuticaCopperCrystallographyZincAnticancerchemistrySettore CHIM/03 - Chimica Generale E Inorganicabiology.proteinDNA supercoilMetal complexeDNACopperDalton transactions (Cambridge, England : 2003)
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Synthesis of Polyfused Heterocycle Derivatives Containing the Dipyridoimidazole Core by Friedländer’s Reaction: Access to Analogs of Ellipticine

2005

Reaction of 3-amino-2-formylimidazo[l,2-a]pyridine with various aldehydes and ketones by Friedlander's methodology afforded an entry to dipyridoimidazole, tri(tetra)azacyclopenta[b]fluorene, tri(tetra)azabenzo[b]-fluorene and triazaindeno[2,1-b]phenanthrene derivatives. Intercalation with a synthetic oligodeoxynucleotide was examined.

StereochemistryIntercalation (chemistry)[CHIM.THER]Chemical Sciences/Medicinal ChemistryFluorene010402 general chemistry01 natural sciencesAnalytical ChemistryEllipticinechemistry.chemical_compound[ CHIM.ORGA ] Chemical Sciences/Organic chemistryPyridine[CHIM.COOR]Chemical Sciences/Coordination chemistryComputingMilieux_MISCELLANEOUSPharmacologybiology[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryOrganic Chemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[ CHIM.THER ] Chemical Sciences/Medicinal ChemistryPhenanthrenebiology.organism_classification0104 chemical scienceschemistryTetra[ CHIM.RADIO ] Chemical Sciences/Radiochemistry[CHIM.RADIO]Chemical Sciences/RadiochemistryHETEROCYCLES
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Interactions of diaryl-polyamines with nucleic acids. Allosteric effects with dinuclear copper complexes

2002

Abstract A series of α,ω-diarylamines with a variable number of ethylenediamine units between terminal naphthylrings shows dramatic affinity changes towards double-stranded nucleic acids, particularly upon complexation with Cu(II) ions. Metal salts alone have under the applied conditions only a negligible effect. The affinity of the metal-free ligands towards nucleic acids shows significant differences to those of the underlying polyamines, with a reversed stabilization of DNA instead of the usually observed preference for RNA. The affinity changes and preliminary NMR studies are in line with intercalation of naphthylrings into the double-stranded nucleic acid, which is hampered by complex …

StereochemistryOrganic ChemistryAllosteric regulationIntercalation (chemistry)RNAEthylenediamineBiochemistrychemistry.chemical_compoundchemistryDrug DiscoveryNucleic acidNucleic acid structureNucleic acid analogueDNATetrahedron Letters
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Pyrimido[5,4-c]pyrrolo[2,1-a]isoquinoline: a new potential DNA-interactive ring system

2003

The acid catalyzed decomposition of the azide 9 failed to give the title compounds, which were however obtained by a Pschorr-type cyclization on reactive 1-(6-aminopyrimidin-5-yl)-pyrroles of type 13. Derivatives of type 14 and 15 were fully characterized by NMR data. Theoretical calculations demonstrated that the new compounds possess properties suitable for DNA- intercalation.

StereochemistryOrganic ChemistryIntercalation (chemistry)Ring (chemistry)DecompositionNmr datalcsh:QD241-441chemistry.chemical_compoundchemistrylcsh:Organic chemistryAcid catalyzedAzideIsoquinolineDNAARKIVOC
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Intercalation effect on hyperfine parameters of Fe in FeSe superconductor with Tc = 42 K

2015

57Fe-Mossbauer spectra of superconducting beta-FeSe, the Li/NH3 intercalate product and a subsequent sample of this intercalate treated with moist He gas have been measured in temperature range 4.7 - 290 K. A correlation is established between hyperfine parameters and critical temperature Tc in these phases. A strong increase of isomer shift upon intercalation is explained by a charge transfer from the Li/NH3 intercalate to the FeSe layers resulting in an increase of Tc up to 42 K. A significant decrease of the quadrupole splitting above 240 K has been attributed to diffusive motion of Li+ ions within the interlamellar space.

SuperconductivitySuperconductivity (cond-mat.supr-con)Materials scienceCondensed Matter - SuperconductivityIntercalation (chemistry)Analytical chemistryGeneral Physics and AstronomyFOS: Physical sciencesQuadrupole splittingAtmospheric temperature rangeHyperfine structureSpectral lineIon
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Intercalation chemistry of superconducting zirconium and hafnium nitride halides

2001

Abstract Lithium intercalation in MNX (M=Zr, Hf; X=Cl, Br) may lead to superconducting compounds with critical temperatures up to 24 K. Electrochemical lithiation experiments agree with the results obtained with chemical methods, as samples with larger capacity on discharge are also those having larger lithium contents after chemical lithiation. Variations exist in the electrochemical profiles of different batches for these compounds indicating differences in the intercalation reaction pathway. High-resolution electron microscopy images confirm the structural model isotypic to SmSI for β-MNX phases. The major part of crystals from ZrNX as well as from the HfNCl samples showing a high lithiu…

SuperconductivityZirconiumMaterials scienceInorganic chemistryIntercalation (chemistry)Analytical chemistrychemistry.chemical_elementHalideNitrideElectrochemistryHafniumchemistryMaterials ChemistryLithiumInternational Journal of Inorganic Materials
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Enhanced CDW Transitions in Nb3X4(X = S, Se, Te): Intercalation and Surface Effects

2004

A x Nb 3 X 4 (A = In, Tl, ZnHg; X = S, Se, Te) compounds show CDW instabilities dependent on the type and concentration of intercalate. Tl or In intercalation flattens the Fermi surfaces and supports CDW formation. In the corresponding DOS spectrum the Fermi level is shifted towards coincidence with a small peak, derived mainly from the Nb dz 2 orbital. Localized modulated regions observed in STM images of Nb 3 X 4 at room temperature represent precursor effects to full CDW formation.

Surface (mathematics)Materials scienceCondensed matter physicsFermi levelIntercalation (chemistry)Fermi surfaceElectronic structureCondensed Matter PhysicsElectronic Optical and Magnetic Materialslaw.inventionsymbols.namesakeSmall peaklawsymbolsScanning tunneling microscopeFermi Gamma-ray Space TelescopeFerroelectrics
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In search of layered antimony(III) materials: synthesis and characterization of oxo-antimony(III) catecholate and further studies on antimony(III) ph…

1998

Abstract A new layered oxo-antimony(III) catecholate, [Sb(C6H4O2)]2O, can be obtained by reacting senarmontite with aqueous catechol. The same reaction performed with valentinite, the other allotropic form of Sb2O3, shows an intermediate hydrate that loses water at about 100°C. Both compounds can be obtained from SbPO4 under appropriate experimental conditions. [Sb(C6H4O2)]2O and the hydrated form, which appear to be layered materials, have been characterized by X-ray diffraction, thermogravimetric/differential thermal analyses, and infrared techniques. Preliminary evidence of a reversible intercalation of pyridine into [Sb(C6H4O2)]2O was collected. Taking into consideration the possible us…

Thermogravimetric analysisAqueous solutionMechanical EngineeringIntercalation (chemistry)Inorganic chemistryInfrared spectroscopychemistry.chemical_elementCondensed Matter Physicschemistry.chemical_compoundchemistryAntimonyMechanics of MaterialsX-ray crystallographyPyridineGeneral Materials ScienceHydrateMaterials Research Bulletin
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A Straightforward Approach to Multifunctional Graphene

2019

Graphene has been covalently functionalized through a one-pot reductive pathway using graphite intercalation compounds (GICs), in particular KC8 , with three different orthogonally protected derivatives of 4-aminobenzylamine. This novel multifunctional platform exhibits excellent bulk functionalization homogeneity (Hbulk ) and degree of addition while preserving the chemical functionalities of the organic addends through different protecting groups, namely: tert-butyloxycarbonyl (Boc), benzyloxycarbonyl (Cbz) and phthalimide (Pht). We have employed (temperature-dependent) statistical Raman spectroscopy (SRS), X-ray photoelectron spectroscopy (XPS), magic angle spinning solid state 13 C NMR …

Thermogravimetric analysisIntercalation (chemistry)010402 general chemistry01 natural sciencesCatalysislaw.inventionPhthalimidesymbols.namesakechemistry.chemical_compoundX-ray photoelectron spectroscopyCompostos orgànicslawMagic angle spinningMaterialsComputingMilieux_MISCELLANEOUS010405 organic chemistryGraphene[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryGeneral ChemistryCombinatorial chemistry0104 chemical scienceschemistrysymbolsSurface modificationRaman spectroscopy
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Carbon Nano-onions: Potassium Intercalation and Reductive Covalent Functionalization

2021

Herein we report the synthesis of covalently functionalized carbon nano-onions (CNOs) via a reductive approach using unprecedented alkali-metal CNO intercalation compounds. For the first time, an in situ Raman study of the controlled intercalation process with potassium has been carried out revealing a Fano resonance in highly doped CNOs. The intercalation was further confirmed by electron energy loss spectroscopy and X-ray diffraction. Moreover, the experimental results have been rationalized with DFT calculations. Covalently functionalized CNO derivatives were synthesized by using phenyl iodide and n-hexyl iodide as electrophiles in model nucleophilic substitution reactions. The functiona…

Thermogravimetric analysisIodideIntercalation (chemistry)02 engineering and technology010402 general chemistryPhotochemistry01 natural sciences7. Clean energyBiochemistryArticleCatalysissymbols.namesakeColloid and Surface ChemistryNucleophilic substitutionchemistry.chemical_classificationElectron energy loss spectroscopytechnology industry and agricultureGeneral Chemistry021001 nanoscience & nanotechnologyEspectroscòpia Raman0104 chemical scienceschemistryCovalent bondsymbolsSurface modificationMaterials nanoestructurats0210 nano-technologyRaman spectroscopyJournal of the American Chemical Society
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