Search results for "RESONANCE"

showing 10 items of 6625 documents

Load-collapse-release cascades of amphiphilic guest molecules in charged dendronized polymers through spatial separation of noncovalent forces.

2012

The ability to pack guest molecules into charged dendronized polymers (denpols) and the possibility to release these guest molecules from subsequently densely aggregated denpols in a load-collapse-release cascade is described. Charged denpols, which constitute molecular objects with a persistent, well-defined envelope and interior, are capable of incorporating large amounts of amphiphilic guest molecules. Simultaneously, multivalent ions can coordinate to the surfaces of charged denpols, leading to counterion-induced aggregation of the already guest-loaded host structures. Thus, although the local guest concentration in denpol-based molecular transport might already be initially high due to…

chemistry.chemical_classificationMolecular StructureChemistryMacromolecular SubstancesPolymersOrganic ChemistryElectron Spin Resonance SpectroscopyNanotechnologymacromolecular substancesGeneral ChemistryPolymerCatalysisChemical physicsDivorceDendrimerAmphiphileMolecular TransportMoleculeHigh potentialMacromoleculeChemistry (Weinheim an der Bergstrasse, Germany)
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Acylated triterpene saponins from the roots of Securidaca longepedunculata.

2009

Abstract Four triterpene saponins , 3- O -β- d -glucopyranosylpresenegenin 28- O -β- d -apiofuranosyl-(1 → 3)-β- d -xylopyranosyl-(1 → 4)-[β- d -apiofuranosyl-(1 → 3)]-α- l -rhamnopyranosyl-(1 → 2)-{4- O -[( E )-3,4,5-trimethoxycinnamoyl]}-β- d -fucopyranosyl ester, 3- O -β- d -glucopyranosylpresenegenin 28- O -β- d -apiofuranosyl-(1 → 3)-β- d -xylopyranosyl-(1 → 4)-[β- d -apiofuranosyl-(1 → 3)]-α- l -rhamnopyranosyl-(1 → 2)-[(6- O -acetyl)-β- d -glucopyranosyl-(1 → 3)]-{4- O -[( E )-3,4,5-trimethoxycinnamoyl]}-β- d -fucopyranosyl ester, 3- O -β- d -glucopyranosylpresenegenin 28- O -β- d -apiofuranosyl-(1 → 3)-β- d -xylopyranosyl-(1 → 4)-[β- d -apiofuranosyl-(1 → 3)]-α- l -rhamnopyranosyl-(…

chemistry.chemical_classificationMolecular StructureChemistryStereochemistryPlant ExtractsChemical structureAcylationSaponinSecuridacaPlant ScienceGeneral MedicineHorticultureSaponinsBiochemistryPresenegeninPlant RootsTriterpenesTriterpenoidSecuridaca longepedunculataTriterpeneMolecular BiologyTwo-dimensional nuclear magnetic resonance spectroscopyPhytochemistry
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Cluster dirhenium(III) cis-dicarboxylates with α-amino acids ligands as mighty selective G4s binders.

2021

The synthesis of four dirhenium(III) cis-dicarboxylates with the α-amino acids residues Asp (I), Glu (II), Phe (III) and Tyr (IV) is presented. The G-quadruplex stabilization potential was evaluated by fluorescence resonance energy transfer - melting analysis. All derivatives show specific binding to c-kit1 quadruplex, while II and IV have also strong stabilization activity to HTelo21 quadruplex. At the same time, the compounds do not show any stabilization activity for ds26 DNA, which suggests unique mechanisms of molecular DNA recognition for these complexes.

chemistry.chemical_classificationMolecular StructureStereochemistrychemistry.chemical_elementDNARheniumG-quadruplexLigandsBiochemistryAmino acidInorganic ChemistryG-Quadruplexeschemistry.chemical_compoundFörster resonance energy transferRheniumchemistryCoordination ComplexesCluster (physics)Fluorescence Resonance Energy TransferHumansheterocyclic compoundsAmino AcidsDNADna recognitionJournal of inorganic biochemistry
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Synthesis and bio-functionalization of magnetic nanoparticles for medical diagnosis and treatment

2011

The synthesis of multifunctional magnetic nanoparticles (NPs) is a highly active area of current research located at the interface between materials science, biotechnology and medicine. By virtue of their unique physical properties magnetic nanoparticles are emerging as a new class of diagnostic probes for multimodal tracking and as contrast agents for MRI. Furthermore, they show great potential as carriers for targeted drug and gene delivery, since reactive agents, such as drug molecules or large biomolecules (including genes and antibodies), can easily be attached to their surface. On the other hand, the fate of the nanoparticles inside the body is mainly determined by the interactions wi…

chemistry.chemical_classificationMultimodal imagingDrug CarriersMaterials scienceBiocompatibilityBiomoleculeContrast MediaNanoparticleNanotechnologyGene deliveryequipment and suppliesMagnetic Resonance ImagingInorganic ChemistrychemistryNeoplasmsHumansMagnetic nanoparticlesLocal environmentSurface modificationMagnetite NanoparticlesDalton Transactions
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ChemInform Abstract: Preparation and Structural Characterization of (Me3SiNSN)2Se, a New Synthon for Sulfur-Selenium Nitrides.

2010

The reaction of (Me(3)SiN)(2)S with SeCl(2) (2:1 ratio) in CH(2)Cl(2) at -70 degrees C provides a route to the novel mixed selenium-sulfur-nitrogen compound (Me(3)SiNSN)(2)Se (1). Crystals of 1 are monoclinic and belong the space group P2(1)/c, with a = 7.236(1) A, b = 19.260(4) A, c = 11.436(2) A, beta = 92.05(3) degrees, V = 1592.7(5) A(3), Z = 4, and T = -155(2) degrees C. The NSNSeNSN chain in 1 consists of Se-N single bonds (1.844(3) A) and S=N double bonds (1.521(3)-1.548(3) A) with syn and anti geometry at the N=S=N units. The N-Se-N bond angle is 91.8(1) degrees. The EI mass spectrum shows a molecular ion with good agreement between the observed and calculated isotopic distributions…

chemistry.chemical_classificationNMR spectra databaseCrystallographyMolecular geometryDouble bondchemistryPolyatomic ionInorganic chemistrySynthonMass spectrumSingle bondGeneral MedicineNuclear magnetic resonance spectroscopyChemInform
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Polymorphic and solvate structures of ethyl ester and carboxylic acid derivatives of WIN 61893 analogue and their stability in solution

2014

3-Ethyl ester- (1) and 3-carboxylic acid-isoxazole (2) derivatives of an antiviral drug analogue WIN 61893 were synthesized and characterized by X-ray crystallography and NMR spectroscopy. Crystallization experiments afforded two polymorphic structures for the ethyl ester derivative and two solvate structures for the carboxylic acid derivative based on their ability to form intermolecular hydrogen bonding interactions with the solvent molecules. The conformations of the derivatives depended greatly on the orientation of the planar isoxazole and phenyl-oxadiazole ring systems with respect to one another and were found to take up perpendicular, linear or tilted conformations. The carboxylic a…

chemistry.chemical_classificationNitrileStereochemistryHydrogen bondDecarboxylationCarboxylic acidGeneral ChemistryNuclear magnetic resonance spectroscopyCondensed Matter PhysicsRing (chemistry)Solventchemistry.chemical_compoundchemistryGeneral Materials ScienceIsoxazoleta116CrystEngComm
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Grafting of polymer chains on the surface of carbon nanotubes via nitroxide radical coupling reaction

2015

Poly(butylene succinate) (PBS) was grafted on the surface of TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy) modified multi-walled carbon nanotubes (MWCNTs) via a nitroxide radical coupling reaction. TEMPO functionalized MWCNTs (MWCNTs-g-TEMPO) were synthesized using the Cu(I)-catalyzed azide/alkyne click chemistry approach and the covalent bond of the nitroxide moieties onto the MWCNTs was confirmed via electron paramagnetic resonance (EPR) spectroscopy. The PBS grafting on the sidewalls of MWCNTs was carried out in solution via peroxide-induced formation of macroradicals and it was confirmed by EPR and attenuated total reflectance Fourier transform infrared analysis. Preliminary rheological …

chemistry.chemical_classificationNitroxide mediated radical polymerizationMaterials sciencePolymers and PlasticsPolymer nanocompositeOrganic ChemistryAlkyne02 engineering and technologyPolymerCarbon nanotube010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceslaw.inventionchemistry.chemical_compoundchemistryCovalent bondlawPolymer chemistryMaterials ChemistryAzide0210 nano-technologyElectron paramagnetic resonancePolymer International
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Functionalization of aliphatic polyesters by nitroxide radical coupling

2014

Functionalized poly(butylene succinate) (PBS) samples were prepared by a post-polymerization method based on the coupling reaction between TEMPO derivatives bearing different functionalities and PBS macroradicals generated by H-abstraction using a peroxide. 4-Benzoyloxy-2,2,6,6-tetramethylpiperidine-1- oxyl (BzO-TEMPO) and 4-(1-naphthoate)-2,2,6,6-tetramethylpiperidine-1-oxyl (NfO-TEMPO), a pro-fluorescent nitroxide, were successfully grafted on PBS, as revealed by MALDI TOF MS and UV-Vis spectroscopy. The functionalization degrees were accurately determined by UV-Vis analysis and confirmed by 1H-NMR spectroscopy. The grafting site was identified by combining theoretical calculations with e…

chemistry.chemical_classificationNitroxide mediated radical polymerizationgenetic structuresPolymers and PlasticsOrganic ChemistrySide reactionBioengineeringPolymerBiochemistryPeroxideCoupling reactionlaw.inventionPolyesterchemistry.chemical_compoundaliphatic polyesterchemistrylawPolymer chemistrySurface modificationElectron paramagnetic resonancenitroxide radicalpolymer functionalizationPolymer Chemistry
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Formation, phase composition, and transformations of Langmuir-Blodgett multi- and monolayers containing Fe

1992

Mono- and multilayers of ferric stearate were formed by the Langmuir-Blodgett technique. Thermodesorption of the hydrocarbon chains results in well defined thin oxidic films. Their reduction to Fe2+ and α-Fe was followed by conversion electron Mossbauer spectroscopy. Resonance lines can be observed even if the Fe coverage is less than one monolayer.

chemistry.chemical_classificationNuclear and High Energy PhysicsAnalytical chemistryResonanceCondensed Matter PhysicsLangmuir–Blodgett filmAtomic and Molecular Physics and Opticschemistry.chemical_compoundHydrocarbonchemistryConversion electron mössbauer spectroscopyStearateMonolayermedicinePhysical chemistryFerricPhysical and Theoretical ChemistryWell-definedmedicine.drugHyperfine Interactions
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Omphalotins E-I, Five Oxidatively Modified Nematicidal Cyclopeptides fromOmphalotus olearius

2009

Omphalotins E–I, oxidatively modified cyclic dodecapeptides, were isolated from mycelial extracts of the basidiomycete Omphalotus olearius, and their structures were determined by NMR spectroscopic and MS methods. Four of the five omphalotins contained an unprecedented N-hydroxylated tricyclic tryptophan derivative. All compounds exhibited strong and selective nematicidal activity against the plant pathogen Meloidogyne incognita with LD90 values between 2 and 5 μg mL–1. Cytotoxic activities were not detected up to 50 μg mL–1. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

chemistry.chemical_classificationOmphalotus oleariusbiologyStereochemistryChemical structureOrganic ChemistryTryptophanBasidiomycotaNuclear magnetic resonance spectroscopybiology.organism_classificationCyclic peptidechemistryMeloidogyne incognitaOrganic chemistryPhysical and Theoretical ChemistryMyceliumEuropean Journal of Organic Chemistry
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