Refine
Year of publication
- 2011 (176) (remove)
Document Type
- Article (129)
- Doctoral Thesis (37)
- Conference Proceeding (4)
- Other (3)
- Review (3)
Is part of the Bibliography
- yes (176)
Keywords
- NMR (4)
- nanoparticles (4)
- Carbohydrates (3)
- Lactones (3)
- Nanopartikel (3)
- Oxygen heterocycles (3)
- Selbstorganisation (3)
- conformational analysis (3)
- ionic liquids (3)
- self-assembly (3)
- Base pairing (2)
- Conformational analysis (2)
- DR-UV-Vis (2)
- Fluorescence spectroscopy (2)
- Metathesis (2)
- Molecular modeling (2)
- NBO analysis (2)
- Photochemistry (2)
- RAFT (2)
- Raman (2)
- Synthetic methods (2)
- TRLFS (2)
- copolymerization (2)
- emulsion polymerization (2)
- ionische Flüssigkeiten (2)
- polyelectrolytes (2)
- quantum chemical calculations (2)
- radical polymerization (2)
- thermoresponsive (2)
- (1)H NMR (1)
- (13)C NMR (1)
- 1,2,3-triazoles (1)
- 2P cross section (1)
- 3-silathianes (1)
- 4,4 '-Bis(tert-butyl)-2,2 '-bipyridine (1)
- 4-silathianes (1)
- 9-Arylfluorenes (1)
- ADMET (1)
- ADMET polymerization (1)
- ATRP (1)
- Ab initio MO computations (1)
- Ab initio quantum chemical methods and calculations (1)
- Adsorption (1)
- Ag/peptide@SiO(2) nanostructures (1)
- Aldol condensation (1)
- Alkynes (1)
- Amphiphilic polymers (1)
- Anisotropic effect (1)
- Anomerization (1)
- Antifouling surfaces (1)
- Antiplasmodial (1)
- Antiretroviral drugs (1)
- Atropselecrivity (1)
- Axial chirality (1)
- Benzoboroxol (1)
- Biaryls (1)
- Bio-inspired mineralization (1)
- Bioactive surfaces (1)
- Biocompatible polymers (1)
- Bioelectrocatalysis (1)
- Biomaterial (1)
- Biopolymer material (1)
- Bioseparation (1)
- Block copolymers (1)
- Blockcopolymer (1)
- Blockcopolymere (1)
- Boronsäure (1)
- C-C coupling (1)
- Calcium phosphate (1)
- Campylobacter jejuni (1)
- Carbazole (1)
- Carbide (1)
- Carbohydrate (1)
- Carbon (1)
- Castor oil (1)
- Cell engineering (1)
- Cellulose (1)
- Chitooligosaccharides (1)
- Chitosan (1)
- Chitosanase (1)
- Chromatographie (1)
- Co-expression (1)
- Collagen (1)
- Condensed thiazolidines (1)
- Conformational equilibria (1)
- Coordination modes (1)
- Copolymerisation (1)
- Copper (1)
- Copper(II) (1)
- Counterions (1)
- Cross-coupling reactions (1)
- Cumarin (1)
- Cycloaddition (1)
- Cyclohexyl esters (1)
- DFT calculation (1)
- DFT calculations (1)
- Decorin (1)
- Depolymerization (1)
- Desymmetrization (1)
- Diazonium salts (1)
- Direct electron transfer (1)
- Dynamic HPLC (1)
- Dynamic NMR (1)
- Dynamic light scattering (1)
- EPR (1)
- ERF (1)
- Eisen (1)
- Electrospray Ionization (1)
- Elektrokatalyse (1)
- Elektronendynamik (1)
- Elektronenkorrelation (1)
- Emulsionen (1)
- Enzyme catalysis (1)
- Flavone (1)
- Fluorescence (1)
- Fluorescence lifetime (1)
- Fluorescent dyes (1)
- Fluorierte Blockcopolymere (1)
- Flüssigphasensynthese (1)
- Formose (1)
- Fragmentation (1)
- Furans (1)
- Gaseous Ions (1)
- Gelatin (1)
- Gele (1)
- Glucose (1)
- Glycosidation (1)
- Glycosides (1)
- Gold (1)
- HAART (1)
- HIV (1)
- Hammett-Brown plots (1)
- Heck coupling (1)
- Heterocycles (1)
- Highly functionalized dimeric triglycerides (1)
- Humic acid (1)
- Hyaluronic acid (1)
- Hybridmaterialien (1)
- Hydrogel (1)
- Hydrogen bonds (1)
- Hydrogen peroxide (1)
- Hydrothermal carbonisation (1)
- Hydrothermalkohle (1)
- Hypoxia (1)
- Insulating films (1)
- Iso-chemical-shielding surfaces (ICSS) (1)
- Janus (1)
- Kathode (1)
- Kinetics (1)
- Klick-Chemie (1)
- Kohlenhydrate (1)
- Kohlenstoff (1)
- Kollagen (1)
- Korrosion (1)
- Kristallisation (1)
- Lactams (1)
- Langmuir monolayers (1)
- Lanthanide ions (1)
- Lanthanides (1)
- Lanthanoide (1)
- Large Stokes-shifts (1)
- Laser-SNMS (1)
- Laserpulse (1)
- Leguminosae (1)
- Li-Ionen-Akkus (1)
- Li-ion batteries (1)
- LiFePO4 (1)
- Lipid domain (1)
- Lucigenin (1)
- Luminescence (1)
- Lumineszenz (1)
- Lysozyme (1)
- Lävulinsäure (1)
- MQAE (1)
- Magnetismus (1)
- Mesokristall (1)
- Mesokristalle (1)
- Mesopores (1)
- Metalation (1)
- Microemulsion (1)
- Microindentation (1)
- Microperoxidase (1)
- Micropores (1)
- Mineralization (1)
- Mizelle (1)
- Mizellen (1)
- Molecular diversity (1)
- Molecular dynamics (1)
- Molecular dynamics simulations (1)
- Molecular rod (1)
- Monolith (1)
- N-acetyl glucosamine derivatives (1)
- N-heterocyclic carbenes (NHC) (1)
- NBO/NCS analysis (1)
- Na+-K+-2Cl(-) cotransporter (1)
- Nanoparticles (1)
- Nanostructure (1)
- Nanostruktur (1)
- Naphthoxazinoquinazolines (1)
- Naphthyridine receptor (1)
- Neurotransmitter (1)
- Neutron spin echo (1)
- Neutron spin-echo spectroscopy (1)
- Nitride (1)
- Nitrobenzyl (1)
- Nucleotide nanosensor (1)
- Olefin self- and cross-metathesis (1)
- Oligosaccharides (1)
- Oxidation (1)
- Palladium (1)
- Peptide (1)
- Peptides (1)
- Phospholipid (1)
- Photo-Dehydro-Diels-Alder reaction (1)
- Photoionisation (1)
- Physical Crosslinking (1)
- Physical Network (1)
- Physikalische Vernetzung (1)
- Plant Material (1)
- Poly(allyl alcohol)s (1)
- Poly-alpha,beta-unsaturated aldehydes (1)
- Polyelektrolyte (1)
- Polyethylene imine (1)
- Polymer chemistry (1)
- Polymer-modified surfaces (1)
- Polymerchemie (1)
- Polymers on surfaces (1)
- Porosimetry (1)
- Potato (1)
- Protein structure (1)
- Quantum chemical calculations (1)
- RAFT-Polymerisation (1)
- Raman spectroscopy (1)
- Rapeseed cake (1)
- Rapeseed oil (1)
- Renewable resources (1)
- Residual dipolar couplings (1)
- Responsive polymers (1)
- Rheologie (1)
- Rheology (1)
- Rhodamine 6G (1)
- Ruthenium (1)
- SANS (1)
- SBFI (1)
- SDS (1)
- Saccharide Recognition (1)
- Sequence analysis (1)
- Silica (1)
- Silica Determination (1)
- Silicon Content (1)
- Small-angle X-ray scattering (1)
- Small-angle neutron scattering (1)
- Sol-Gel (1)
- Solanum tuberosum (1)
- Solid phase (1)
- Solubility (1)
- Solvent effects (1)
- Spatial NICS (1)
- Spiro compound (1)
- Stem (1)
- Stimuli-responsive polymers (1)
- Substituent effects (1)
- Superoxide (1)
- Supramolecular Interactions (1)
- Supramolekularen Wechselwirkungen (1)
- Surfactant micelles (1)
- TOF-SIMS (1)
- TRANES (1)
- TRES (1)
- Tandem mass spectrometry (1)
- Templating (1)
- Tenside (1)
- Tephrosia purpurea (1)
- Terpurinflavone (1)
- Thiol-ene addition (1)
- Through-space NMR shieldings (TSNMRS) (1)
- Transition metals (1)
- Tuber (1)
- Valerolacton (1)
- Vernetzung (1)
- Vinylogous N-acyliminium ion (1)
- Vorstufe (1)
- WANG-Linker (1)
- WANG-linker (1)
- X-ray photoelectron spectroscopy (1)
- X-ray structure (1)
- Zeolites (1)
- Zeolithe (1)
- Zuckererkennung (1)
- acidity constants (1)
- adsorption (1)
- alkynes (1)
- alpha,omega-Dienes (1)
- amphiphilic particles (1)
- analytical methods (1)
- anthracenes (1)
- aqueous systems (1)
- atom transfer radical polymerization (ATRP) (1)
- azides (1)
- benzoboroxole (1)
- block copolymer (1)
- block copolymers (1)
- boronic acid (1)
- cGMP (1)
- caged Verbindungen (1)
- caged compounds (1)
- carbides (1)
- cathode (1)
- charge transport (1)
- chiral nanoparticles (1)
- chromatography (1)
- cis,cis-Tricyclo[5.3.0.0(2,6)]dec-3-enes (1)
- click chemistry (1)
- computational chemistry (1)
- confocal Raman microscopy (1)
- conformational transitions (1)
- copolymers (1)
- core-shell structures (1)
- corrosion (1)
- coumarine (1)
- cross-linking (1)
- crystallization (1)
- cycloaddition (1)
- density functional calculations (1)
- diazo compounds (1)
- dibenzocyclooctane (1)
- dibenzylbutane (1)
- dynamic NMR (1)
- electrocatalysis (1)
- electron correlation (1)
- electron dynamics (1)
- emulsions (1)
- endo-Mode cyclization (1)
- epithelial ion transport (1)
- fiber-optical spectroscopy (1)
- fluorinated Blockcopolymers (1)
- fluoropolymers (1)
- formose (1)
- gels (1)
- hexafluoropropene (1)
- humic acid (1)
- hybrid materials (1)
- hydrophil (1)
- hydrophilic (1)
- hydrothermal (1)
- hydrothermal carbon (1)
- hydrothermale Carbonisierung (1)
- imidazolium (1)
- imines (1)
- ionic liquid (1)
- iron (1)
- isomerization (1)
- kinetics (polym.) (1)
- lanthanide ions (1)
- laser pulses (1)
- levulinic acid (1)
- lignans (1)
- liquid phase synthesis (1)
- low-temperature NMR spectroscopy (1)
- luminescence (1)
- macrocycles (1)
- magnetism (1)
- mesocrystal (1)
- mesocrystals (1)
- mesoporous (1)
- mesoporös (1)
- micelle (1)
- micelles (1)
- monolith (1)
- morphology (1)
- nanosilver (1)
- neurotransmitter (1)
- nitrides (1)
- nitrobenzyl (1)
- nitrogen heterocycles (1)
- nonlinear optics (1)
- oligo(ethylene glycol) (1)
- oligo(ethyleneglycol) (1)
- organic chemistry (1)
- organic light-emitting diodes (1)
- organische Chemie (1)
- oxidation (1)
- oxidative stress (1)
- p-Hydroxycinnamic acids (1)
- palladium (1)
- peptide-templated materials (1)
- peroxides (1)
- phase behavior (1)
- phase transitions (1)
- phenols (1)
- photochemistry (1)
- photoionization (1)
- photon density wave spectroscopy (1)
- physiolgischer pH (1)
- physiological pH (1)
- poly(N-isopropyl acrylamide) (1)
- poly(N-isopropylacrylamide) (1)
- polyampholytes (1)
- polybutadiene (1)
- polymer modification (1)
- polymerization (1)
- polystyrenes (1)
- porous materials (1)
- porphyrinoids (1)
- poröse Materialien (1)
- precursor (1)
- protein carbonyls (1)
- quantum chemistry (1)
- quinoline-2,4(1H,3H)-diones (1)
- rare earths (1)
- reversibility (1)
- rheology (1)
- ring-opening polymerization (1)
- silica (1)
- silver nanoparticles (1)
- singlet oxygen (1)
- sol-gel (1)
- solid phase (1)
- solubility (1)
- solvent influence (1)
- spirocycles (1)
- sulfimides (1)
- sulfur heterocycles (1)
- supercritical CO(2) (1)
- supercritical carbon dioxide (1)
- surfactants (1)
- temperaturschaltbar (1)
- terminal alkynes (1)
- tetrapyrroles (1)
- thermisch schaltbare Polymere (1)
- thermochemistry (1)
- thermomorphism (1)
- thermosensitive polymers (1)
- valerolactone (1)
- vinylidene fluoride (1)
- viscosity (1)
- wässrige Systeme (1)
Institute
- Institut für Chemie (176) (remove)
The title compound was prepared by the reaction of 1,4,10,13-tetraoxa-7,16-diazacyclo-octadecane with 4-chloro-2-methyl-phenoxyacetic acid in a ratio of 1:2. The structure has been proved by the data of elemental analysis, IR spectroscopy, NMR ((1)H, (13)C) technique and by X-ray diffraction analysis. Intermolecular hydrogen bonds between the azonium protons and oxygen atoms of the carboxylate groups were found. Immunoactive properties of the title compound have been screened. The compound has the ability to suppress spontaneous and Con A-stimulated cell proliferation in vitro and therefore can be considered as immunodepressant.