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Ethylene oxide polystyrene anion

Anionic polymerization of ethylene oxide by living carbanions of polystyrene was first carried out by Szwarc295. A limited number of methods have been reported in the preparation of A-B and A-B-A copolymers in which B was polystyrene and A was poly(oxyethylene)296-298. The actual procedure was to allow ethylene oxide to polymerize in a vacuum system at 70 °C with the polystyrene anion initiated with cumyl potassium in THF299. The yields of pure block copolymers are usually limited to about 80% because homopolymers are formed300. ... [Pg.25]

It has been shown recently (10) that such block structures could be tailored precisely by the general method summarized hereabove. It is indeed possible to convert the hydroxyl end-group of a vinyl polymer PA (f.i. polystyrene, or polybutadiene obtained by anionic polymerization terminated with ethylene oxide),into an aluminum alcoholate structure since it is well known that CL polymerizes in a perfectly "living" manner by ring-opening insertion into the Al-0 bond (11), the following reaction sequence provides a direct access to the desired copolymers, with an accurate control of the molecular parameters of the two blocks ... [Pg.311]

The first block (polybutadiene or polystyrene) is prepared by anionic polymerization, under high vacuum, in THF dilute solution (less than 5%), at low temperature (—70 °C) with cumylpotassium as initiator. Then, the living polymer is transformated into a hydroxylated polymer (PV—OH) by addition of ethylene oxide under vacuum, or into a carboxylated polymer (PV-COOH) by addition of carbon dioxide under vacuum. [Pg.147]

The synthesis and purification of polystyrene methacryloyl macromonomers (PS-MA) in the molecular weight range Mn= 1000-2000 g mol 1 by living anionic polymerization of styrene (S), termination with ethylene oxide (EO), and subsequent reaction with methacrylic chloride has already been described in detail elsewhere [180] (see also Scheme 16). In this context it has to be emphasized that the hydroxyethyl-terminated PS-MA macromonomer precursor (PS-OH) as obtained after purification of the crude PS-OH by silica column chromatography (cyclohexane/dichloromethane 1/1 v/v) and as charged in the PS-MA synthesis still contains up to about 15 wt-% of non-functionalized polystyrene (PS-H). This PS-H impurity of the PS-MA macromonomer does not interfere with the PS-MA synthesis and the subsequent TBA/PS-MA copolymerization and is easily and conveniently removed from the resulting PTBA-g-PS graft copolymer (see below). [Pg.31]

Other multifunctional initiators include star polymers prepared from initiators via living radical or other living polymerizations. In particular, all of the star polymers via metal-catalyzed living polymerization, by definition, carry a halogen initiating site at the end of each arm, and thus they are potentially all initiators. Thus, star-block copolymers with three polyisobutylene-Mock-PMMA arms and four poly-(THF) -A/oc/F polystyrene or poly(THF)-Woc/c-polysty-rene-Wock-PMMA were synthesized via combination of living cationic and copper-catalyzed living radical polymerizations.381,388 Anionically synthesized star polymers of e-caprolactone and ethylene oxide have... [Pg.500]

Tsitsilianis et al. recently published [245] preliminary results on the micelliza-tion behavior of anionically synthesized amphiphilic heteroarm star copolymers with polystyrene and poly(ethylene oxide) branches in THF and water. The former solvent is not very selective for one of the segments whereas the latter is strongly selective for PEO. The apparent molecular weights found for the micelles in THF were two orders of magnitude larger than the ones measured for the unimers. By increasing concentration an increase in the depolarization ratio was observed supporting the conclusion that multimolecular micelles are formed by this kind of miktoarm star copolymer. [Pg.116]

The discovery of the anionic ring-opening polymerization of silicon-bridged[l]ferrocenophanes enabled the synthesis of well-defined, near-monodisperse poly(ferrocenylsilane) homo- and block copolymers. PFS was combined with polystyrene [38], polyisoprene [39], poly(dimethylsilox-ane) [40], poly(ethylene oxide) [41], poly(ferrocenylphenylphosphine) [42], poly(aminoalkyl methacryate) [43] and recently with poly(methyl methacrylate) [44,45] blocks. [Pg.93]

Block copolymers consisting of segments with widely separated solubility characteristics have generated considerable interest because of their unusual surfactant properties. In fact, one of the earliest commercial block copolymers were the Wyandotte "Pluronics." These were poly(propylene oxide-b-ethylene oxide) prepared by sequential addition of ethylene oxide to sodium alkoxide initiated propylene oxide (37,38). Szwarc (39) and others (40,41) prepared poly(styrene-b-ethylene oxide) by addition of ethylene oxide to polystyrene anions in tetrahydrofuran. Other syntheses of AB or ABA block copolymers of styrene-ethylene oxide include sequential addition in various solvents, and coupling reactions (42,43). [Pg.91]

New block copolymers of polystyrene and poly(e-caprolactone) have recently been prepared with a combination of coordination catalyst and anionic polymerization( An amorphous styrene block was prepared by conventional anionic polymerization at room temperature, and terminated with ethylene oxide. After hydrolysis the terminal - OH groups were substituted by oxo-Al-Zn alkoxide. A crystalline block was then added by coordination polymerization of e-caprolactam. [Pg.93]

There were also attempts to calibrate the SEC columns with help of broad molar mass dispersity poplymers but this is less lehable. The most common and well credible SEC cahbration standards are linear polystyrenes, PS, which are prepared by the anionic polymerizatioa As indicated in section 11.7, according to lUPAC, the molar mass values determined by means of SEC based on PS calibration standards are to be designated polystyrene equivalent molar masses . Other common SEC calibrants are poly(methyl methaciylate)s, which are important for eluents that do not dissolve polystyrenes, such as hexafluoroisopropanol, further poly(ethylene oxide)s, poly(vinyl acetate)s, polyolefins, dextrans, pullulans, some proteins and few others. The situation is much more complicated with complex polymers such as copolymers. For example, block copolymers often contain their parent homopolymers (see sections 11.8.3, 11.8.6 and 11.9). The latter are hardly detectable by SEC, which is often apphed for copolymer characterization by the suppliers (compare Figure 16). Therefore, it is hardly appropriate to consider them standards. Molecules of statistical copolymers of the same both molar mass and overall chemical composition may well differ in their blockiness and therefore their coils may assume distinct size in solution. In the case of complex polymers and complex polymer systems, the researchers often seek support in other characterization methods such as nuclear magnetic resonance, matrix assisted desorption ionization mass spectrometry and like. [Pg.283]


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Anion oxidation

Anionic polystyrene, oxidized

Anionic polystyrenes

Oxide anion

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