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Polymethacrylamide

Other polyacrylamides and polymethacrylamides (4, 5)55 56 have been prepared and their chiral recognition abilities as CSPs have been evaluated. Chiral stationary phase 5 shows high recognition for several drugs. [Pg.166]

Synthetic polymers This type of chiral selectors (polyacrylamides, polymethacrylamide, etc.) was first developed by the group of Blaschke by polymerization of chiral monomers with cross-linking agents to form a three-dimensional polymer network. [Pg.476]

Farther growth of the polymeric chain proceeds in the nsnal manner. Compared to the polymeric materials obtained by conventional methods, the mechanochemically synthesized polyacryl and polymethacrylamides have lower molecular weights (Simonescu et al. 1983). Acrylonitrile, styrene, e-caprolactam, and isoprene as well as aryl and methacrylamides have special optimal duration of the polymerization on grinding (Oprea and Popa 1980). In the case of the aryl and methacrylamides, the polymerization proceeds slowly, usually between 24 and 72 h. After that, some acceleration takes place and the process is completed in 96 h (in total). [Pg.284]

Shea KJ, Stoddard GJ, Shavelle DM, Wakui F, Choate RM. Synthesis and characterization of highly cross-linked polyacrylamides and polymethacrylamides—a new class of macro-porous polyamides. Macromolecules 1990 23 4497-4507. [Pg.427]

While the batch process is the dominant one in current use, researchers and companies have attempted to create continuous bioreactor systems. Lopez et al. immobilized Candida rugosa in polymethacrylamide hydrazide beads and polyurethane foam 3 with the intent to achieve the continuous production of lipase enzymes. Despite flow problems with the polyurethane foam, it showed high lipolytic activity. Biomass buildup was problematic. Feijoo et al. immobilized Phanerochaete chry-sosporium on polyurethane foam in packed bed bioreactors under near-plug flow conditions. Continuous lignin peroxidase production was accomplished, the rate of which was studied as a function of recycle ratio. [Pg.171]

Similar grafting experiments by the emulsion technique were described (34) in the system vinyl chloride/copolymer butyl methacrylate-methacrylic acid and in the reverse system, and also in the system styrene/polyvinyl chloride. In this last case again as in homogenous medium, the inverse process failed (vinyl chloride on polystyrene). Grafted acrylonitrile copolymers were also prepared in order to improve their dyeability, by polymerizing acrylonitrile in emulsion in the presence of many different polymers as polyvinyl alcohol, polymethacrylamide and polyvinylpyrrolidone (119, 120, 121), polyvinyl acetate and polyacrylic acid (115), wool (224,225), proteins (136), etc. [Pg.185]

Various addition polymers were synthesized and used for the chiral resolution purposes, but helical polymethacrylates and polymethacrylamides are more effective and useful for chiral resolution. However, the chiral resolution on other polymers is also discussed. [Pg.327]

Blaschke et al. [54—56] synthesized polyacrylamide and polymethacrylamide containing chiral side chains. In order to make CSPs, these polymers were bonded to silica gel chemically [54-56]. The CSP obtained by /V-acrylol-(.S)-phenylalanine ethyl ester was commercialized by Merck Chemical Company by the trade name ChiraSpher. The racemic compounds resolved are those capable of forming hydrogen-bondings (i.e., amides, imides, carboxylic acids, and alcohols). It has been reported that nonpolar solvents like benzene and toluene individually or their mixtures were the best mobile phases. In addition to these CSPs, other amide CSPs were prepared and tested for the chiral resolution [57,58]. [Pg.332]

Polyacrylamide and Polymethacrylamide Containing Nucleic Acid Bases... [Pg.29]

A CSP consists of a chiral selector, which either alone constitutes the stationary phase or which has been immobilised to a solid phase. The chiral selector is a low molecular weight compound or a polymer, either synthetic or natural. A broad range of CSPs has been developed. Examples of CSPs that have been used successfully include polysaccharides, such as cellulose and its derivatives [6] and cyclodex-trins [7], and proteins, e.g. bovine serum albumin, aj-acid glycoprotein, cellulase, trypsin and a-chymotrypsin [8]. Several different synthetic polymers have also proven to be useful CSPs, for example the Blaschke-type CSPs (polyacrylamides and polymethacrylamides) [9] and the Pirkle-type CSPs [10]. [Pg.395]

When solid monomers of acrylamide (AM) and methacrylamide (MAM) were subjected to plasma initiation, only trace amounts of insoluble polymers were obtained. Now if aqueous solutions of AM and MAM were used in the plasma initiated polymerization high conversions were again achievable upon post-polymerization. Polyacrylamide was found to be completely soluble, whereas polymethacrylamide forms a gel. It is of interest to note that no poljnner is formed with post-polymerization alone without plasma initiation... [Pg.254]

Pins polystyrene- or polymethacrylamide-dimethylacrylamide-fcopolymerised) derived matrices grafted on polyethylen crowns which arc attached on top of pins. The pins usually are assembled in the typical 96-well plate format. This technology originally developed by Geysen et a/.. 57.5S for the parallel synthesis of polypetide libraries has found wide applications also for the synthesis of small-molecular-weight compound collections... [Pg.26]

Methanol[67-56-l] (methyl alcohol) is a clear, colorless liquid with a characteristic odor. It is hygroscopic and miscible in all proportions with water as well as with many organic solvents. It is less soluble in fats and oils, and is only partially miscible with aliphatic hydrocarbons. Numerous inorganic substances (e.g., many salts) are soluble in methanol. Methanol has a good solvency for polar resins, cellulose nitrate, and ethyl cellulose. However, oil-modified alkyd resins and polymers, with the exception of poly(vinyl acetate), poly(vinyl ethers), polyvinylpyrolidone and polymethacrylamide, are insoluble. [Pg.354]

Polyesters Polyvinylpyrrolidone Polymethacrylamide Rubbers Polysiloxanes Polyvinylalcohol Polyacroleine Polytrifluorochloroethylene... [Pg.645]

Side-Chain-Type Polymers. We synthesized two types of side-chain-type polymers, polymethacrylamide (7/) and polymethacrylate, both containing triphenylamine or tetraphenyldiamine as functional groups. As illustrated in Figure 3, hole transport in these polymers is due to hole movement along the triphenylamine moieties and hopping between chains. [Pg.384]


See other pages where Polymethacrylamide is mentioned: [Pg.139]    [Pg.157]    [Pg.29]    [Pg.135]    [Pg.139]    [Pg.151]    [Pg.157]    [Pg.332]    [Pg.59]    [Pg.13]    [Pg.13]    [Pg.107]    [Pg.107]    [Pg.348]    [Pg.313]    [Pg.314]    [Pg.62]    [Pg.107]    [Pg.107]    [Pg.167]    [Pg.10]    [Pg.11]    [Pg.645]    [Pg.384]    [Pg.548]   
See also in sourсe #XX -- [ Pg.139 ]

See also in sourсe #XX -- [ Pg.157 ]

See also in sourсe #XX -- [ Pg.254 ]

See also in sourсe #XX -- [ Pg.157 ]




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