Search results for "Institut für Chemie"

showing 10 items of 16 documents

Solubilization control by redox-switching of polysoaps

2008

Reversible changes in the self-organization of polysoaps may be induced by controlling their charge numbers via covalently bound redox moieties. This is illustrated with two viologen polysoaps, which in response to an electrochemical stimulus, change their solubility and aggregation in water, leading from homogeneously dissolved and aggregated molecules to collapsed ones and vice verse. Using the electrochemical quartz crystal microbalance (EQCM), it could be shown that the reversibility of this process is better than 95% in 16 cycles.

Aqueous solutionPolymers and PlasticsChemistryInorganic chemistryViologenGeneral ChemistryQuartz crystal microbalanceCondensed Matter PhysicsElectrochemistryPhotochemistryRedoxCovalent bondddc:540Materials ChemistrymedicineMoleculeInstitut für ChemieSolubilitymedicine.drug
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Photoluminescence study of terbium-exchanged ultrastable Y zeolites: Number of species, photoluminescence decays and decay-associated spectra

2008

Terbium-exchanged ultrastable Y (USY) zeolites were investigated by using time-resolved photoluminescence spectroscopy techniques and methods. To determine the distribution of terbium species in USY zeolites together with their photoluminescence properties, several analysis methods for the time-resolved luminescence spectra were used such as the area normalization of time-resolved photoluminescence spectra, singular value decomposition, global nonlinear least squares, and the maximum entropy. Except for a questionable long lifetime, small contribution of a terbium species with lifetime of 1.9¿2.1 ms, all the experimental and analysis results converged to a two terbium species distribution w…

LanthanidePhotoluminescenceSilylationAnalytical chemistryFísicaGeneral Physics and Astronomychemistry.chemical_elementTerbiumQuímica analíticaCiència dels materialsSpectral linechemistryNon-linear least squaresInstitut für ChemieTime-resolved spectroscopySpectroscopy
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Monolayers and Langmuir-Blodgett Multilayers of Discotic Liquid Crystals?

2008

The field of monolayer and multilayer films of discotic LCs is at its very beginning. The scope and limitations of this preparation method have not yet been explored, and little is known about the structures obtainable. However, the potential access to extraordinary, ordered thin films is fascinating, and will stimulate research in the future.

Materials scienceField (physics)Mechanical EngineeringDiscotic liquid crystalNanotechnologyGeneral MedicineGeneral ChemistryLangmuir–Blodgett filmCatalysisPreparation methodMechanics of Materialsddc:540MonolayerInstitut für ChemieGeneral Materials ScienceThin filmAngewandte Chemie International Edition in English
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Second-harmonic generation in Langmuir–Blodgett monolayers of stilbazium salt and phenylhydrazone dyes

1988

The second-order nonlinear optical susceptibilities χ(2) of several phenylhydrazone and stilbazium salt dyes in Langmuir–Blodgett monolayers have been determined from second-harmonic-generation measurements. Three of the substances demonstrated χ(2) values greater than 10−6 electrostatic units, although two of the three did not absorb light significantly at the second-harmonic wavelength.

Materials sciencebusiness.industryAnalytical chemistrySecond-harmonic generationNonlinear opticsElectrostatic unitsStatistical and Nonlinear PhysicsLangmuir–Blodgett filmAtomic and Molecular Physics and OpticsOpticsAttenuation coefficientddc:540MonolayerInstitut für ChemieThin filmbusinessRefractive indexJournal of the Optical Society of America B
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Amphiphilic dyes for nonlinear optics: Dependence of second harmonic generation on functional group substitution

2008

Materials sciencebusiness.industryMechanical EngineeringSubstitution (logic)Nonlinear opticsSecond-harmonic generationchemistry.chemical_compoundOpticschemistryMechanics of MaterialsChemical physicsFunctional groupMonolayerAmphiphileddc:540Institut für ChemieGeneral Materials Sciencebusiness
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Isoflavones and Rotenoids from the Leaves of Millettia oblata ssp. teitensis

2017

A new isoflavone, 8-prenylmilldrone (1), and four new rotenoids, oblarotenoids A−D (2−5), along with nine known compounds (6−14), were isolated from the CH2Cl2/CH3OH (1:1) extract of the leaves of Millettia oblata ssp. teitensis by chromatographic separation. The purified compounds were identified by NMR spectroscopic and mass spectrometric analyses, whereas the absolute configurations of the rotenoids were established on the basis of chiroptical data and in some cases by single-crystal X-ray crystallography. Maximaisoflavone J (11) and oblarotenoid C (4) showed weak activity against the human breast cancer cell line MDA-MB-231 with IC50 values of 33.3 and 93.8 μM, respectively. peerReviewed

Millettia oblata ssp. teitensisflavonoiditddc:540Institut für Chemieisoflavoneshernekasvitluonnonaineetrotenoids
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Cytotoxicity of isoflavones and biflavonoids from Ormocarpum kirkii towards multi-factorial drug resistant cancer.

2019

Abstract Background While incidences of cancer are continuously increasing, drug resistance of malignant cells is observed towards almost all pharmaceuticals. Several isoflavonoids and flavonoids are known for their cytotoxicity towards various cancer cells. Purpose The aim of this study was to determine the cytotoxicity of isoflavones: osajin (1), 5,7-dihydroxy-4ˈ-methoxy-6,8-diprenylisoflavone (2) and biflavonoids: chamaejasmin (3), 7,7″-di-O-methylchamaejasmin (4) and campylospermone A (5), a dimeric chromene [diphysin(6)] and an ester of ferullic acid with long alkyl chain [erythrinasinate (7)] isolated from the stem bark and roots of the Kenyan medicinal plant, Ormocarpum kirkii. The m…

Pharmaceutical ScienceApoptosisPlant Roots03 medical and health scienceschemistry.chemical_compound0302 clinical medicineCell Line TumorDrug DiscoveryCytotoxic T cellBiflavonoidsHumansddc:610Cytotoxicity030304 developmental biologyPharmacologychemistry.chemical_classificationMembrane Potential Mitochondrial0303 health sciencesBiflavonoidsPlants MedicinalPlant ExtractsCell CycleBiflavonoidFabaceaeIsoflavonesMolecular biologyAntineoplastic Agents PhytogenicIsoflavonesKenyaDrug Resistance MultipleComplementary and alternative medicinechemistryCell cultureApoptosisDrug Resistance Neoplasm030220 oncology & carcinogenesisCaspasesCancer cellPlant BarkMolecular MedicineInstitut für ChemieReactive Oxygen SpeciesPhytomedicine : international journal of phytotherapy and phytopharmacology
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Preparation and Structure of Diexo-Oxanorbornane-fused 1,3-Heterocycles

2004

Via the reaction of diexo-oxanorbornanedicarboxylic anhydride with toluene, the diexo-aroylcarboxylic acid (3a) was prepared, which exists partly as the tautomeric lactol (3b). With bifunctional reagents, 3a yields fused heterocycles containing three-six rings. Thus, alkylenediamines result in imidazole- and 1,3-diazepine-fused oxygen- bridged isoindolones (6a,b), alkanolamines form the oxazole- and 1,3-oxazine-fused oxanorbornene derivatives (7a-c), and o-phenylenediamine undergoes cyclization to furnish the condensed benzimidazole (8). The reaction of 3a with diexo- aminonorbornanecarbohydrazide yields a pyrimidopyridazine containing six condensed rings (9). In a similar reaction with die…

PharmacologyCyclopentadieneLactolArylOrganic ChemistrySubstituentRetro-Diels–Alder reactionMedicinal chemistryTautomerAnalytical Chemistrychemistry.chemical_compoundchemistryInstitut für ChemieOrganic chemistryImidazoleOxazoleHETEROCYCLES
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Monolayers of rod-shaped and disc-shaped liquid crystalline compounds at the air-water interface

2008

Calamitic (rod-shaped) and discotic (disc-shaped) thermotropic liquid crystalline (LC) compounds were spread at the air-water interface, and their ability to form monolayers was studied. The calamitic LCs investigated were found to form monolayers which behave analogously to conventional amphiphiles such as fatty acids. The spreading of the discotic LCs produced monolayers as well, but with a behaviour different from classical amphiphiles. The areas occupied per molecule are too small to allow the contact of all hydrophilic groups with the water surface and the packing of all hydrophobic chains. Various molecular arrangements of the discotics at the water surface to fit the spreading data a…

Polymers and PlasticsChemistryAir water interfaceLiquid crystallineThermotropic crystalExternColloid and Surface ChemistryChemical engineeringLiquid crystalAmphiphileMonolayerddc:540Materials ChemistryMoleculeOrganic chemistryInstitut für ChemiePhysical and Theoretical Chemistry
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Relaxation and charge transport in mixtures of zwitterionic polymers and inorganic salts

2009

Dielectric spectroscopy is employed to analyze the molecular dynamics and the charge transport in mixtures of zwitterionic polymers of the type poly(3-[N-(omega-methacryloyloxyalkyl)-N, N-dimethylammonio]propanesulfonate) with sodium iodide in the frequency range of 10(2) Hz-10(7) Hz and in the temperature range of 110 K-400 K. The amount of inorganic salt added varies from 0-200 mol-% relative to the number of zwitterionic groups present in the polymer, contributing strongly to the conductivity. One relaxation process is observed whose relaxation rate depends strongly on the length of the aliphatic spacer between the polymethacrylate main chain and the zwitterionic group. Exhibiting an Arr…

Polymers and PlasticsChemistryOrganic ChemistryInorganic chemistryAnalytical chemistryConcentration effectDielectricActivation energyConductivityCondensed Matter PhysicsDielectric spectroscopyddc:540Polymer chemistryMaterials ChemistrySide chainInstitut für ChemieRelaxation (physics)Ionic conductivityPhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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