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Atom transfer radical polymerization styrene

Polystyrene-Woc -polysulfone-/ /oc -polystyrene and poly(butyl acrylate)-Woc -polysulfone-/ /oc -poly(butyl acrylate) triblock copolymers were prepared using a macroinitiator.214 The hydroxyl-terminated polysulfone was allowed to react with 2-bromopropionyl bromide, an atomic transfer radical polymerization (ATRP) initiator, in the presence of pyridine. The modified macroinitiator could initiate die styrene polymerization under controlled conditions. [Pg.359]

Star polymers are a class of polymers with interesting rheological and physical properties. The tetra-functionalized adamantane cores (adamantyls) have been employed as initiators in the atom transfer radical polymerization (ATRP) method applied to styrene and various acrylate monomers (see Fig. 21). [Pg.229]

Block copolymers were synthesized by a combination of fipase-catalyzed polymerization and atom transfer radical polymerization (ATRE). " " At first, the polymerization of 10-hydroxydecanoic acid was carried out by using lipase CA as catalyst. The terminal hydroxy group was modified by the reaction with a-bromopropionyl bromide, followed by ATRP of styrene using CuCE2,2 -bipyridine as catalyst system to give the polyester-polystyrene block copolymer. Trichloromethyl-terminated poly(e-CL), which was synthesized by lipase CA-catalyzed polymerization with 2,2,2-trichloroethanol initiator, was used as initiator for ATRP of styrene. [Pg.227]

The last decades have witnessed the emergence of new living Vcontrolled polymerizations based on radical chemistry [81, 82]. Two main approaches have been investigated the first involves mediation of the free radical process by stable nitroxyl radicals, such as TEMPO while the second relies upon a Kharash-type reaction mediated by metal complexes such as copper(I) bromide ligated with 2,2 -bipyridine. In the latter case, the polymerization is initiated by alkyl halides or arenesulfonyl halides. Nitroxide-based initiators are efficient for styrene and styrene derivatives, while the metal-mediated polymerization system, the so called ATRP (Atom Transfer Radical Polymerization) seems the most robust since it can be successfully applied to the living Vcontrolled polymerization of styrenes, acrylates, methacrylates, acrylonitrile, and isobutene. Significantly, both TEMPO and metal-mediated polymerization systems allow molec-... [Pg.32]

In this review, synthesis of block copolymer brushes will be Hmited to the grafting-from method. Hussemann and coworkers [35] were one of the first groups to report copolymer brushes. They prepared the brushes on siUcate substrates using surface-initiated TEMPO-mediated radical polymerization. However, the copolymer brushes were not diblock copolymer brushes in a strict definition. The first block was PS, while the second block was a 1 1 random copolymer of styrene/MMA. Another early report was that of Maty-jaszewski and coworkers [36] who reported the synthesis of poly(styrene-h-ferf-butyl acrylate) brushes by atom transfer radical polymerization (ATRP). [Pg.129]

Ruthenium(II)-NHC systems ean be used for atom transfer radical polymerization (ATRP). Generally, similar results as for the analogous phosphine complexes are obtained. For the ATRP of styrene and methyl methacrylate (MMA) [(NHC)2peBr2] was found to rival copper(I)-based systems and to yield poly (MMA) with low polydispersities. Polymerizations based on olefin metathesis that are catalyzed by ruthenium-NHC complexes are discussed separately vide supra). [Pg.50]

NasruUah Ml, Webster DC (2006) Polymerization of styrene and 1-butyl acrylate by atom-transfer radical polymerization - high throughput approach. Polymer Prepr 47 217-218... [Pg.14]

Becer CR, Paulus RM, Hoppener S et al. (2008) Synthesis of poly(2-ethyl-2-oxazoline)-h-poly(styrene) copolymers via a dual initiator route combining cationic ring opening polymerization and atom transfer radical polymerization. Macromolecules 41 5210-5215... [Pg.60]

Indenylidene compounds VIII, K, XXI, XXIII, XXVIIIa and XXVIIIb act as atom transfer radical polymerization catalysts for the polymerization of methyl methacrylate and styrene in high yields and with good control (Table 8.7). The catalytic activity can be dramatically improved by transforming the complexes into cationic species by treatment with AgBp4 [61]. [Pg.273]

The synthesis of mixed peroxides formed from /-butyl hydroperoxide and carbon-centred radicals has been studied. The reactions were strongly effected by solvents as well as catalytic amounts of Cun/Fem. The kinetic data suggest that the conditions for the Ingold-Fischer persistent radical effect are fulfilled in these cases.191 The use of Cu /Cu" redox couples in mediating living radical polymerization continues to be of interest. The kinetics of atom-transfer radical polymerization (ATRP) of styrene with CuBr and bipyridine have been investigated. The polymer reactions were found to be first order with respect to monomer, initiator and CuBr concentration, with the optimum CuBr Bipy ratio found to be 2 1.192 In related work using CuBr-A-pentyl-2-... [Pg.126]

Frechet and coworkers recently described how living free radical polymerization can be used to make dendrigrafts. Either 2,2,6,6-tetramethylpiperidine oxide (TEMPO) modified polymerization or atom transfer radical polymerization (ATRP) can be used [96] (see Scheme 10). The method requires two alternating steps. In each polymerization step a copolymer is formed that contains some benzyl chloride functionality introduced by copolymerization with a small amount of p-(4-chloromethylbenzyloxymethyl) styrene. This unit is transformed into a TEMPO derivative. The TEMPO derivative initiates the polymerization of the next generation monomer or comonomer mixture. Alternatively, the chloromethyl groups on the polymer initiate an ATRP polymerization in the presence of CulCl or CuICl-4,4T dipyridyl complex. This was shown to be the case for styrene and n-butylmethacrylate. SEC shows clearly the increase in molecu-... [Pg.204]

Louie and Grubbs prepared an iron-based catalyst for atom transfer radical polymerization (ATRP) [49]. By heating a solution of Iz Prim and FeX2 (X = Br, Cl), crystals of Fe(Iz Prim)2X2 were obtained. These complexes mediated the homogeneous ATRP of styrene and methyl methacrylate with... [Pg.175]

The controlled emulsion polymerization of styrene using nitroxide-mediated polymerization (NMP), reversible addition-fragmentation transfer polymerization (RAFT), stable free radical polymerization (SFR), and atom transfer radical polymerization (ATRP) methods is described. The chain transfer agent associated with each process was phenyl-t-butylnitrone, nitric oxide, dibenzyl trithiocarbonate, 1,1-diphenylethylene, and ethyl 2-bromo-isobutyrate, respectively. Polydispersities between 1.17 and 1.80 were observed. [Pg.595]

Controlled Polymerization of Styrene Using n-Butyl Acrylate and 1-Hexene [Atom Transfer Radical Polymerization ATRP]... [Pg.596]

Nakagawa [5] prepared poly(styrene-b-isobutylene) through atom transfer radical polymerization that had good weatherability properties. [Pg.716]

Figure 33 Surface initiated block copolymerization of styrene and methyl methacrylate through atom transfer radical polymerization ... Figure 33 Surface initiated block copolymerization of styrene and methyl methacrylate through atom transfer radical polymerization ...
The reaction with aryl radicals of this kind has found an interesting application in the direct polymerization of vinylic monomers like styrene, methyl methycrylate (MMA), or hydroxyethyl methacrylate (HEMA) on the diamond. Furthermore, the covalent attachment of an initiator molecule allows for an atom transfer radical polymerization (ATRP) to take place immediately on the diamond surface and results in a covalently bound composite material (Figure 6.41). [Pg.435]

Destarac M, Bessiere J-M, Boutevin B (1998) Atom transfer radical polymerization of styrene initiated by polychloroalkanes and catalyzed by CuCI/2, 2-bipyridine A kinetic and mechanistic study. J Polymer Sci A Polym Chem 36 2933-2947... [Pg.80]


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See also in sourсe #XX -- [ Pg.187 ]




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