Atom transfer radical polymerization reverse

Atom transfer radical polymerization Reversible addition-... 

Wang et al. [31] used a surface-initiated reverse atom transfer radical polymerization (reverse ATRP) technique to synthesize the well-controlled nanostructure of polymer brushes from silicon wafer. PMMA brushes were prepared by modifying the surface of the silicon substrate with peroxide... 

The facile and reversible reaction of propagating species with transition metal halide complexes to form a polymeric halo-compound is one of the key steps in atom transfer radical polymerization (ATRP, see Section 9.4). 

ORl OX w di-Miutyl peroxyoxalalc deactivation by reversible chain transfer and bioinolecular aclivaiion 456 atom transfer radical polymerization 7, 250, 456,457, 458,461.486-98 deactivation by reversible coupling and untmolecular activation 455-6, 457-86 carbon-centered radical-mediated poly nierizaiion 467-70 initiators, inferlers and iriiters 457-8 metal complex-mediated radical polymerization 484... 

While in most of the reports on SIP free radical polymerization is utihzed, the restricted synthetic possibihties and lack of control of the polymerization in terms of the achievable variation of the polymer brush architecture limited its use. The alternatives for the preparation of weU-defined brush systems were hving ionic polymerizations. Recently, controlled radical polymerization techniques has been developed and almost immediately apphed in SIP to prepare stracturally weU-de-fined brush systems. This includes living radical polymerization using nitroxide species such as 2,2,6,6-tetramethyl-4-piperidin-l-oxyl (TEMPO) [285], reversible addition fragmentation chain transfer (RAFT) polymerization mainly utilizing dithio-carbamates as iniferters (iniferter describes a molecule that functions as an initiator, chain transfer agent and terminator during polymerization) [286], as well as atom transfer radical polymerization (ATRP) were the free radical is formed by a reversible reduction-oxidation process of added metal complexes [287]. All techniques rely on the principle to drastically reduce the number of free radicals by the formation of a dormant species in equilibrium to an active free radical. By this the characteristic side reactions of free radicals are effectively suppressed. 

RATRP reverse atom transfer radical polymerization... 

Representative structm-e is Si/Si02//tethered block-6-outer block ATRP—atom transfer radical polymerization, RATRP—reverse atom transfer radical polymerization, RAFT—reversible addition fragmentation transfer polymerization... 

Scheme 2 Synthesis of surface-immobilized diblock copolymer brush (Si/Si02//PS-fc-PMMA) using reverse atom transfer radical polymerization and ATRP...

Atom transfer radical polymerization (ATRP) [52-55]. Active species are produced by a reversible redox reaction, catalyzed by a transition metal/ligand complex (Mtn-Y/Lx). This catalyst is oxidized via the halogen atom transfer from the dormant species (Pn-X) to form an active species (Pn ) and the complex at a higher oxidation state (X-Mtn+1-Y/Lx). 

The need to better control surface-initiated polymerization recently led to the development of controlled radical polymerization techniques. The trick is to keep the concentration of free radicals low in order to decrease the number of side reactions. This is achieved by introducing a dormant species in equilibrium with the active free radical. Important reactions are the living radical polymerization with 2,2,4,4-methylpiperidine N-oxide (TEMPO) [439], reversible addition fragment chain transfer (RAFT) which utilizes so-called iniferters (a word formed from initiator, chain transfer and terminator) [440], and atom transfer radical polymerization (ATRP) [441-443]. The latter forms radicals by added metal complexes as copper halogenides which exhibit reversible reduction-oxidation processes. 

In this paper, we first present a model study on blending a a,co-3,5-dinitrobenzoate PDMS and free 9H-carbazole-9-ethanol, in order to check whether the recently proposed 1 1 stoechiometry between carbazole and dinitrobenzoate molecules indeed applies (Scheme 1). [26] Then, we describe the preparation of triblock copolymers, poly[2-(N-carbazolyl)ethyl methacrylate]-fc-PDMS-fc-poly[2-(N-carbazolyl)ethyl methacrylate] (P(CzEMA)-fe-PDMS-fc-P(CzEMA)), using Atom Transfer Radical Polymerization (ATRP), and their blending with the acceptor-functionalized PDMS. In both studies, the physical association and thermal reversibility of these were followed by different techniques, including UV-Vis spectroscopy, DSC or Rheology. 

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. 

Fig. 19 Reversible attachment of a Cu(I)-catalyst to a solid support via triple hydrogen bonds, acting as a reversible catalyst for atom transfer radical polymerization (ATRP)...

Fe(III) species can also be employed in a so-called reverse or alternative atom-transfer radical polymerization (section II.B.9). A mixture of FeCl3 and PPh3 can mediate a controlled polymerization of MMA in the presence of AIBN to give similarly narrow MWDs MJMn = 1.1—1.3).80 An ammonium halide such as />Bu4NBr can be employed in place of PPh3 as a ligand for FeBr3 in the AIBN-initiated radical polymerization.74... 

The so-called reverse atom-transfer radical polymerization is feasible in aqueous emulsion too. This system enables the formation of initiating radical species in the water phase with the use of water-soluble initiators such as 1-39, 1-40, and 1-41 as in conventional emulsion radical polymerization.184,249,252,255 The copper-catalyzed emulsion radical polymerization of nBMA afforded polymers with narrow MWDs (MJMn = 1.1—1.4), but the Mn values were much higher than the calculated values due to the termination between the initiating radicals in the aqueous phase.184,255 The emulsions are relatively stable and their particle sizes are around 100—300... 

Controlled free-radical polymerization (CFRP) has been used successfully to produce block, graft, and other controlled architecture copolymers within the last decade for a variety of free radically polymerizable monomers. The main techniques include reversible addition fragmentation and transfer (RAFT) polymerization, stable free-radical polymerization (SFRP) mediated by nitroxide/alkoxyamine based radicals, atom transfer radical polymerization (ATRP), diphenyl ethylene (DPE) mediated polymerization, and novel precipitation/emulsion polymerization based methods like free-radical retrograde precipitation polymerization (FRRPP). ... 

Radical polymerizations can be controlled by addition of a suitable metal complex, which reversibly transforms the free radicals into a dormant species. Such is the case in atom transfer radical polymerization (ATRP) [155, 156]. Contrary to the... 

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