Graft copolymers, anionic

A Cationic Graft Copolymer of Lignin. The applications of the anionic graft copolymers described above are many but the negative charge on the polymer or the behavior of the anionic polymer under application conditions often limit the utility of these materials. 

Serefoglou E, Obeidisse J, Staikos G (2007) Characterization of the soluble nanoparticles formed through coulombic interaction of bovine serum albumin with anionic graft copolymers at low pH. Biomacromolecules 8 1195-1199. doi 10.1021/hm061094t... 

Grafting can also occur in the amide nitrogen, either through an anionic-type mechanism which is beheved to operate when ethylene oxide [75-21 -8] and similar copolymers are grafted to polyamides, or through a polycondensation mechanism when secondary amides are formed as graft copolymers (70). 

It was found that the sulfate radical anion S04 produced photochemically in Scheme (46) is responsible for generating the cellulose derivative macroradicals by hydrogen abstraction, which added the vinyl monomer to produce the grafted copolymer. The main disadvantage of this method is the production of large quantities of undesirable homopolymers in addition to the grafted copolymers. 

Very few graft copolymers based on poly(arylene ether)s have been synthesized, probably because of their chemical inertness. Klapper et al. reported grafting the polystyrene or polyisoprene onto the poly(ether ether ketone ketone) (PEEKK) by anionic deactivation.229 The carbonyl groups on tire backbone can be attacked by the polystyrene monoanion or polyisoprene anion (Mn about 3000). Due to the steric hindrance only about 30% of tire carbonyl groups can be reacted. 

In a similar manner polyisoprene-polyethylene oxide block copolymers can prepared301. It is surprising that the poly(methyl methacrylate) anion can be successfully used for the polymerization of ethylene oxide without chain transfer302. Graft copolymers are also prepared by successive addition of ethylene oxide to the poly-... 

Anionic grafting of 0-propiolactone onto acrylate copolymers was extensively studied333-33s. ... 

Recently it has been shown that anionic functionalization techniques can be applied to the synthesis of macromonomers — macromolecular monomers — i.e. linear polymers fitted at chain end with a polymerizable unsaturation, most commonly styrene or methacrylic ester 69 71). These species in turn provide easy access to graft copolymers upon radical copolymerization with vinylic or acrylic monomers. 

Two types of well defined branched polymers are acessible anionically star-shaped polymers and comb-like polymers87 88). Such macromolecules are used to investigate the effect of branching on the properties, 4n solution as well as in the the bulk. Starshaped macromolecules contain a known number of identical chains which are linked at one end to a central nodule. The size of the latter should be small with respect to the overall molecular dimensions. Comb-like polymers comprise a linear backbone of given length fitted with a known number of randomly distributed branches of well defined size. They are similar to graft copolymers, except that backbone and branches are of identical chemical nature and do not exhibit repulsions. 

Anionic polymerization techniques can also be applied to the synthesis of graft copolymers 6 7 87 1U). Kennedy s classification 134) is used here as shown in Scheme 5. 

The purpose of this review is to show how anionic polymerization techniques have successfully contributed to the synthesis of a great variety of tailor-made polymer species Homopolymers of controlled molecular weight, co-functional polymers including macromonomers, cyclic macromolecules, star-shaped polymers and model networks, block copolymers and graft copolymers. 

Kennedy and co-workers 2 117) used the changing effect of the initiation ability of the Lewis acids according to Eq. (17) and the termination tendency of the anion formed according to Eq. (18) in order to obtain telechelic polymers , block copolymers and graft copolymers in a controlled manner. Quantum chemical calculations provide the possibility to discuss structural influences which work on the equilibrium Eq. (19) and therefore on the stability of the two adjacent ions. 

Results and Discussion. Of the 12 samples of starch graft copolymer synthesized, half were hydrolyzed to anionic polyelectrolytes. Synthesis data on these 6 samples are given in Table 2. These particular samples were chosen for hydrolysis because the samples can be intercompared to see the effect of synthesis variables on ultimate product properties. Samples 5, 8, and 11 have the same mole ratio of cerium ion to starch backbone, N, in their reaction mixture. Samples 7, 8, and 9 all have the same refctable mass per starch molecule,... 

TABLE 2. Hydrolysis of Graft Copolymers to Anionic Terpolymers ... 

Strongly anionic, highly water-soluble, graft copolymers of starch can be made by adding 2-propenamide and sodium 2,2-dimethyl-3-imino-4-oxohex-5-ene-1-sulfonate (Na DMIH) to the polymerization reactions. See references 43 and 56 for a discussion of these polymers. 

A radical initiator based on the oxidation adduct of an alkyl-9-BBN (47) has been utilized to produce poly(methylmethacrylate) (48) (Fig. 31) from methylmethacrylate monomer by a living anionic polymerization route that does not require the mediation of a metal catalyst. The relatively broad molecular weight distribution (PDI = (MJM ) 2.5) compared with those in living anionic polymerization cases was attributed to the slow initiation of the polymerization.69 A similar radical polymerization route aided by 47 was utilized in the synthesis of functionalized syndiotactic polystyrene (PS) polymers by the copolymerization of styrene.70 The borane groups in the functionalized syndiotactic polystyrenes were transformed into free-radical initiators for the in situ free-radical graft polymerization to prepare s-PS-g-PMMA graft copolymers. 

A combination of TEMPO living free radical (LFRP) and anionic polymerization was used for the synthesis of block-graft, block-brush, and graft-block-graft copolymers of styrene and isoprene [201]. The block-graft copolymers were synthesized by preparing a PS-fo-poly(styrene-co-p-chloromethylstyrene) by LFRP [Scheme 110 (1)], and the subsequent re-... 

Concerning the synthesis of graft copolymers, Jedlinski et al. have prepared poly(MMA-g-(3BL) copolymers via anionic grafting of 3BL from a modified PMMA backbone [85]. PMMA chains were partially saponified by potassium hydroxide and complexed by 18C6 crown ether so as to act as multifunctional mac-... 

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