Search results for "Copolymer"
showing 10 items of 1003 documents
Organo-catalyzed synthesis of aliphatic polycarbonates in solvent-free conditions
2012
A new efficient and expeditious route to the synthesis of aliphatic polycarbonates, in solvent-free conditions and using 1-n-butyl-3-methylimidazolium-2-carboxylate (BMIM-2-CO2) as a catalyst precursor, is described. The protocol consists of a two-step polymerization process involving the transesterification of dimethyl carbonate (DMC) with linear alkane diols and leading to high molecular weight homopolymers. The reaction went to completion quantitatively with the liberation of methanol as the only by-product. The in situ formation of N-heterocyclic carbene species resulting from BMIM-2-CO2 decarboxylation is suggested to be a key feature of the condensation process. The protocol was then …
On the formation of inclusion complexes at the solid/liquid interface of anchored temperature-responsive PNIPAAM diblock copolymers with γ-cyclodextr…
2017
The thermal responsive behavior of adsorbed layers of diblock copolymers of poly(N-isopropylacrylamide) (PNIPAAM) and poly((3-acrylamidopropyl)trimethylammonium chloride) (PAMPTMA(+)) with γ-cyclodextrin (γ-CD) at the solid/liquid interface has been investigated using three in situ techniques: null ellipsometry, quartz–crystal microbalance with dissipation monitoring, and neutron reflectometry. The measurements provided information about the adsorbed amounts, the layer thickness, hydration and viscoelastic properties, and the interfacial structure and composition. The copolymers adsorb to silica with the cationic PAMPTMA(+) blocks sitting as anchors in a flat conformation and the PNIPAAM ch…
Immobilization of functionalized lipids in a random poly(methacrylate) copolymer monolayer
1995
It is shown that a monolayer of random poly(methacrylate) copolymer with a hydrophobic and a hydrophilic substituent exhibits a transition from the fluid to amorphous state. Above this transition any amphiphilic molecules mixed with the monolayer are immobile. Furthermore, such functionalized lipids are immobilized in the monolayer during the Langmuir-Blodgett transfer. The hydrophilic head-groups of the biotin-lipids remain on the formerly water-adjacent side of the monolayer, even if this side is exposed to air
Polyacrylonitrile block copolymers for the preparation of a thin carbon coating around TiO2 nanorods for advanced lithium-ion batteries.
2013
Herein, a new method for the realization of a thin and homogenous carbonaceous particle coating, made by carbonizing RAFT polymerization derived block copolymers anchored on anatase TiO2 nanorods, is presented. These block copolymers consist of a short anchor block (based on dopamine) and a long, easily graphitizable block of polyacrylonitrile. The grafting of such block copolymers to TiO2 nanorods creates a polymer shell, which can be visualized by atomic force microscopy (AFM). Thermal treatment at 700 °C converts the polyacrylonitrile block to partially graphitic structures (as determined by Raman spectroscopy), establishing a thin carbon coating (as determined by transmission electron m…
Stabilizing nanostructured lithium insertion materials via organic hybridization: A step forward towards high-power batteries
2014
Abstract Herein, we present the electrochemical characterization of carbon-coated TiO 2 nanorods, obtained by carbonizing RAFT (reversible addition fragmentation chain transfer) polymerization derived block copolymers anchored on anatase TiO 2 nanorods. These carbon-coated TiO 2 nanorods show an improved electrochemical performance in terms of first cycle reversibility, specific capacity, cycling stability, and high rate capability. More importantly, however, the structural disordering observed in the uncoated TiO 2 nanorods by means of galvanostatic and potentiodynamic cycling as well as ex situ XRD analysis, does not occur for the carbon-coated material. Preventing this structural disorde…
Some New Copolymers by Ionic Polymerization
1980
In the first part the cationic polymerization of a homologous series of cyclic ether–acetals with ring sizes of 11, 14, and 17 atoms is described. During the polymerization of triethylene glycol formal (TGF) an equilibrium is reached and besides high polymers cyclic oligomers are formed. The oligomers and the polymers are built up of a regular sequence of one oxymethylene unit and three oxyethylene units –[–(OCH2) (OC2H4)3–]–x. They are therefore be labelled a “sequenced copolymer.” The equilibrium concentrations of the cyclic oligomers with a polymerization degree from 2 to 15 follow the Jacobson–Stockmayer equation. The 14- and 17-membered monomers POC and HOC forms cyclic oligomers and h…
Biomedical Applications of Polylactide (PLA) and Its Copolymers.
2018
n/a
Polyaspartylhydrazide Copolymer-Based Supramolecular Vesicular Aggregates as Delivery Devices for Anticancer Drugs
2008
In this paper we report on three different hydrophilic copolymers based on alpha,beta-polyaspartylhydrazide (PAHy) bearing butyric groups in the side chain (C 4) (PAHy-C 4) or a combination of butyric groups and positive charged residues ((carboxypropyl)trimethylammonium chloride, CPTACl) (PAHy-C 4-CPTA) that were synthesized and used for the preparation of new supramolecular vesicular aggregates (SVAs) containing gemcitabine as an antitumor drug. Gemcitabine-loaded SVAs containing synthesized PAHy derivatives were characterized from the physicochemical and technological point of view and the in vitro toxicity and anticancer activity on two different human cancer cell lines, i.e., CaCo-2 (h…
Beads of Acryloylated Polyaminoacidic Matrices Containing 5-Fluorouracil for Drug Delivery
2002
Spherical polymeric microparticles have been prepared by a reverse phase suspension polymerization technique. The starting polymer was alpha,beta-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA), partially derivatized with glycidylmethacrylate (GMA). PHEA-GMA copolymer (PHG) was crosslinked in the presence of N,N'-dimethylacrylamide (DMAA) or N,N'-ethylenebisacrylamide (EBA). 5-fluorouracil was incorporated into PHG-DMAA or PHG-EBA beads both during and after the crosslinking process. Swelling studies revealed a high affinity toward aqueous medium, influenced by the presence of 5-fluorouracil. The in vitro release study showed that the release rate depends on the chemical structure of the beads…
Gelchromatographie. 8. Mitt.: Vernetzte copolymere des vinylacetats
1969
Die Eigenschaften von vernetzten Copolymeren des Vinylacetats wurden in Abhangigkeit von den Herstellungsbedingungen gepruft. Als Vernetzungsmittel dienten Divinyladipat und Butandiol-(1.4)-divinylather. Mit homogen-vernetzten Gelen konnen Ausschlusmolekulargewichte bis etwa 4000 erzielt werden: zwischen dem spezifischen Gelbettvolumen und dem Ausschlusmolekulargewicht besteht eine lineare Beziehung. Die heterogen-vernetzende Copolymerisation des Vinylacetats in Gegenwart verschiedener inerter Verdunnungsmittel fuhrt zu Gelen mit Ausschlusmolekulargewichten uber 106. Die vernetzten Copolymeren wurden durch ihre scheinbare Dichte, durch die Aufnahme von Losungs- und Fallungsmitteln, durch di…