Ring opening reactions, polystyren

Ring-opening reaction of epichlorohydrin with polystyrene anion... 

The existence of a ring opening reaction in polystyrene has also been supported by ESCA spectroscopy. The ESCA spectra of photoirradiated polystyrene films in air or oxygen (Fig. 3.56) show the relevant Ci, and Ojj core levels [466,467,1702]. From a starting profile consisting of a main photoemission peak at 285.0 eV (arising from the C—H components in the backbone chain and pendant phenyl groups) and an- n shake-up satellite... 

The ring opening reaction was also supported by the studies of photooxidation of low molecular model compounds of polystyrene, e.g. 2-phenyl butane (5.85) [1360, 1361] ... 

Crosslinking of oxazoline containing polymers by ring-opening reaction (PP, polypropene PS, polystyrene). 

By using a combination of RAFT and ring opening polymerization (ROP), (polyethylene oxide) methyl ether)(polystyrene)(poly(L-lactide) 3-miktoarm star terpolymers have been successfully synthesized [182]. The synthetic approach involved the reaction of the cw-functionalized - OH group of the poly(ethylene oxide) methyl ether with maleic anhydride under conditions where only one hydroxyl group can be esterified (MPEO). The double bond... 

By utilizing a combination of RAFT and cationic ROP, the synthesis of [poly(methyl methacrylate)][poly(l,3-dioxepane)][polystyrene] miktoarm star terpolymers was achieved [182], The approach involved the synthesis of PS functionalized with a dithiobenzoate group by RAFT polymerization and subsequent reaction with hydroxyethylene cinnamate (Scheme 98). The newly created hydroxyl group was then used for the cationic ring opening polymerization of 1,3-dioxepane (DOP). The remaining dithiobenzoate group was used for the RAFT polymerization of methyl methacrylate. 

The use of these initiators to polymerize LA814 and methylglycolide815 has been reported to proceed in a well-controlled fashion. Block copolymers such as PCL-b-PLA have also been prepared. Elimination of PrOH from the reaction of (270) with preformed hydroxyl terminated polymers, followed by lactone polymerization, yields diblocks of CL with polystyrene or polybutadiene.816 The preparation of an ABA triblock has also been reported (A = CL, B = LA) since propagating chains of PLA do not initiate CL ring opening, (270) was pretreated with hydroxy terminated (PCL-b-PLA)-OH 814... 

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 ... 

Bachmann and Seebach [159] have reported the preparation and characterization of cyclic lactones (MeCHCH2C(0)0)n, where n = 4 and 8. The reaction product between butyl lithium in benzene and the solid polystyrene support PS-C6H4CH2NH2 leads to a lithiated species that can be represented as PS-Cfd bCI 12N11 Li(BuI i)x, where x 4 is active in the ring-opening of the cyclic esters L-lactide, rac-lactide, and 2,5-morpholinediones, leading to their respective cyclic oligoesters and cyclodepsipeptides (Fig. 49) [160]. The... 

Several types of copper-loaded polymer have been prepared. Hydrocarbon spacers were introduced between polystyrene and copper (23). Six synthetically useful copper-promoted reactions including a Diels-Alder reaction, an epoxide ring-opening, and an aryl iodide hydrolysis were examined by using the polymeric catalyst [34]. Use of the copper-loaded polymers often either improved the yield or reduced the reaction time compared with those for conventional copper salts. 

The synthesis of polystyrene-g-polytetrahydrofurane [188] was achieved by ATR copolymerization of methacrylic PTHF macromonomer, MA-PTHF, with styrene (Scheme 105). The PTHF macromonomer was synthesized by cationic ring opening polymerization of THF with acrylate ions, formed by the reaction of methacryloyl chloride and AgC104. The polydispersity indices of the graft copolymers determined by SEC ranged between 1.3-1.4. Kinetic studies revealed that the relative reactivity ratio of the macromonomer to St was independent of the molecular weight of PTHF. 

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