Search results for "cationic polymerization"
showing 10 items of 441 documents
Anomalien bei der kationischen copolymerisation von trioxan. 32. Mitt. über polyoxymethylene
1967
Die kationische Copolymerisation von Trioxan mit Styrol, 1,3-Dioxolan und anderen Comonomeren last sich wegen folgender Nebenreaktionen nicht durch die ubliche MAYO-sche Copolymerisationskinetik erfassen: 1. Depolymerisation der Trioxymethylenbausteine zu Formaldehyd wahrend der Induktionszeit und daher Bildung sehr styrolreicher bzw. dioxolanreicher Prapolymerer. 2. Bildung und Polymerisation von Formaldehyd, welcher wahrend der gesamten Polymerisation in seiner ceiling-Gleichgewichtskonzentration zugegen ist. 3. Abspaltung oxacyclischer Verbindungen von den aktiven Kettenenden; Bildung von Tetroxan und 4-Phenyl-1,3-dioxan bei der Copolymerisation von Trioxan mit Styrol. 4. Ubertragung am …
1968
In order to determine the concentration of active centers, polymerizations are terminated by addition of sodium alkoxide. This yields alkoxy endgroups which after acid hydrolysis of the isolated and purified polymers are determined by gaschromatography of the produced alcohol. In cationic polymerization of anhydrous formaldehyde at −78°C under certain reaction conditions a fast and quantitative initiation reaction and no kinetic chain termination have been observed. Presumably living polymers are obtained. The unexpected decrease in the rate of polymerization after a certain conversion is ascribed to hindrance of monomer diffusion in the crystalline polymer in which the active centers are i…
ChemInform Abstract: Poly(alkylidenamines) Dendrimers as Scaffolds for the Preparation of Low-Generation Ruthenium Based Metallodendrimers
2011
The aim of this article is to highlight the use of nitrile-functionalized poly(alkylidenamines) dendrimers as building blocks for the preparation of low-generation ruthenium based cationic metallodendrimers having in view potential biomedical applications. Air-stable poly(alkylidenamines) nitrile dendrimers, peripherally functionalized with the ruthenium moieties [Ru(η5-C5H5)(PPh3)2]+ or [RuCl(dppe)2]+, have been prepared, characterized and are being studied for their anticancer activity. The followed strategy is based on the biological advantages associated with low-generation dendrimers, the known activity of ruthenium compounds as anticancer drugs and the stability of these dendrimers at…
Untersuchungen über die Polymerisation von 2-Formyl-Δ5-dihydropyran
1963
Nach einer kurzen Beschreibung des dimeren Acroleins (2-Formyl-Δ5-dihydropyran) wird die spontane und katalysierte Polymerisation untersucht. Fur die Spontanpolymerisate wird die Struktur eines Polyacetals vorgeschlagen. Borfluoridatherat und Eisen-III-chlorid fuhren zu Polymeren mit ganz anderen Eigenschaften. An Hand der chemischen Reaktionen und IR-Spektren werden die moglichen Strukturen der kationischen Polymerisate diskutiert. After characterization of the acrolein dimer (2-formyl-Δ5-dihydropyran) its spontaneous and catalytic polymerization has been investigated. A polyacetal structure has been suggested for the spontaneous polymer. Borofluorid-etherate and iron-trichloride lead to p…
Phospholylmethano P-chirogenic-phosphine-borane as P-(η2-BH3)-chelating ligands of rhodium (I): Synthesis, characterization and asymmetric hydrogenat…
2021
International audience; The stereoselective synthesis of new phospholylmethano P-chirogenic-phosphine-borane was achieved by P-C bond formation of the bridge, using electrophilic or nucleophilic P*-building blocks. These P1CH2P2*.BH3 ligands behaved as chelating (κ1-P1)-(η2-BH3) entities towards the cationic rhodium(I) centre. The resulting chiral rhodium complexes were tested in asymmetric rhodium catalyzed hydrogenation of methyl 2-(acetamido)acrylate.
Crystal structure of 4-{2-[4-(dimethylamino)phenyl]diazen-1-yl}-1-methylpyridinium iodide
2015
The molecular geometry of the ionic title compound, C14H17N4+·I−or DAZOP+·I−, is essentially featureless. Regarding the crystal structure, in addition to the obvious cation–anion Coulombic interactions, the packing is mostly directed by non-covalent interactions involving both ring systems, as well as the iodide anion. It consists of cationic molecules aligned along [101] and disposed in an antiparallel fashion while linked into π-bonded dimeric entities by a stacking contact involving symmetry-related phenyl rings, with a centroid–centroid distance of 3.468 (3) Å and a slippage of 0.951 Å. The dimers are, in addition, sustained by a number of C—H...I and I...π (I...centroid = 3.876 Å) inte…
Gene delivery agents possessing antiradical activity: self-assembling cationic amphiphilic 1,4-dihydropyridine derivatives
2013
Seventeen 1,4-dihydropyridine (1,4-DHP) amphiphiles including differently substituted pyridinium, pyrazinium, N-methyl piperidinium or N-methyl morpholinium moieties as the cationic head-group of the molecule have been designed and synthesised. 1,4-DHP amphiphiles have been earlier proposed as a promising tool for plasmid DNA (pDNA) delivery in vitro. In this work the ability of the 1,4-DHP amphiphiles to self-assemble, to bind pDNA and to transfer it into the cells as well as the cytotoxicity of 1,4-DHP amphiphiles–pDNA complexes was studied. Furthermore, antiradical activity (ARA) of the 1,4-DHP derivatives was determined. We have revealed that all new 1,4-DHP amphiphiles possessed self-a…
Electrostatically Driven Complexation of Liposomes with a Star-Shaped Polyelectrolyte to Low-Toxicity Multi-Liposomal Assemblies
2013
Anionic liposomes are electrostatically complexed to a star-shaped cationic polyelectrolyte. Upon complexation, the liposomes retain their integrity and the resulting liposome-star complexes do not dissociate in a physiological solution with 0.15 M NaCl. This provides a multi-liposomal container for possible use as a high-capacity carrier.
Acidic Co-Catalysts in Cationic Gold Catalysis.
2016
A systematic study on the effects of Lewis or Bronsted acid co-catalysts in gold-catalyzed reactions was undertaken using representative reactions (O-, N-, and C-nucleophilic additions to alkynes). Through these reactions, it was demonstrated that an acidic co-catalyst can increase the catalyst turnover significantly, enabling practical reaction rates at competitive catalyst loadings (<1 mol %). Further investigation is currently underway to improve the understanding of the subtle principles underlying these experimental observations.
Measurements on the temperature dependence of the cationic polymerization of styrene in CH2Cl2 with CF3SO3H as catalyst
1979
The cationic polymerization of styrene in CH2Cl2 with CF3SO3H as catalyst and at low monomer concentrations shows, at −15°C, −45°C and −60°C, the same formal dependence on monomer concentration. The dependence on the catalyst concentration is approximately but not exactly of a third order.