Polymerization trans

Termination by primary radicals in vinyl polymerization. Trans. 

Jenkins, A. D. Transfer to solvent and retardation in vinyl polymerization. Trans. Faraday Soc. 54, 1885 (1958). 

Lanthanum derivatives containing either bis(2-ethylhexyl)phosphate or 4-nonylphenoxide ligands have been found effetive in polymerizing trans-butadiene (5). 

It is known that CoCl2/Al(C2H5)Cl can polymerize trans-l,3-pentadiene but not the cis isomer [263]. This suggests that a two-point coordination is required. Several reaction schemes that provide for an attack at either Ci or at C4 positions were proposed over the years [263]. One mechanism for polymerization of butadiene suggests that complexes of the catalysts in solvents of low dielectric constant will either act as ion pairs or as independent solvated entities. Also, the growing chain may be bound by either a 71 or a a linkage, and it is suspected that a crnitinuous u n isomerism is possible [264] ... 

Co(NCSeCH2CH2SeCN)Cl2 room 5.01 Gouy probably octahedral, polymeric trans-form suggested 68G18... 

K. Akagi, H. Tanaka, R. Toyoshima, H. Shirakawa, S5mtheses of thiophene derivatives with liquid crystalline substituents and their polymerizations, Trans. Mater. Res. Soc. Jpn., 15A, 513-516 (1994). 

Molybdenum is also a smoke suppressant for poly(vinyl chloride). It promotes the formation of cis- rather than the trans-polymeric decomposition products which ate the precursors for smoke. The sources for molybdates ate Climax Performance Material Cotp. and Sherwin WiUiams. 

Unlike other synthetic polymers, PVDF has a wealth of polymorphs at least four chain conformations are known and a fifth has been suggested (119). The four known distinct forms or phases are alpha (II), beta (I), gamma (III), and delta (IV). The most common a-phase is the trans-gauche (tgtg ) chain conformation placing hydrogen and fluorine atoms alternately on each side of the chain (120,121). It forms during polymerization and crystallizes from the melt at all temperatures (122,123). The other forms have also been well characterized (124—128). The density of the a polymorph crystals is 1.92 g/cm and that of the P polymorph crystals 1.97 g/cm (129) the density of amorphous PVDF is 1.68 g/cm (130). 

Polymerization catalyzed by free radicals occurs with sorbic acid. The polymers (3) formed have high molecular weights with linear stmctures the trans form of the residual double bond is preserved (13). 

Polymerization. Chloroprene is normally polymerized with free-radical catalysts in aqueous emulsion, limiting the conversion of monomer to avoid formation of cross-linked insoluble polymer. At a typical temperature of 40°C, the polymer is largely head-to-taH in orientation and trans in configuration, but modest amounts of head-to-head, cis, 1,2, and 3,4 addition units can also be detected. A much more regular and highly crystalline polymer can be made at low temperature (11). Chloroprene can also be polymerized with cationic polymerization catalysts, giving a polymer with... 

Natural mbber (Hevea) is 100% i7j -l,4-polyisoprene, whereas another natural product, gutta-percha, a plastic, consists of the trans-1,4 isomer. Up until the mid-1900s, all attempts to polymerize isoprene led to polymers of mixed-chain stmcture. 

A living cationic polymeriza tion of isobutylene and copolymeriza tion of isobutylene and isoprene has been demonstrated (22,23). Living copolymerizations, which proceed in the absence of chain transfer and termination reactions, yield the random copolymer with narrow mol wt distribution and well-defined stmcture, and possibly at a higher polymerization temperature than the current commercial process. The isobutylene—isoprene copolymers are prepared by using cumyl acetate BCl complex in CH Cl or CH2CI2 at —30 C. The copolymer contains 1 8 mol % trans 1,4-isoprene... 

Distribution of the monomer units in the polymer is dictated by the reactivity ratios of the two monomers. In emulsion polymerization, which is the only commercially significant process, reactivity ratios have been reported (4). IfMj = butadiene andM2 = acrylonitrile, then = 0.28, and r2 =0.02 at 5°C. At 50°C, Tj = 0.42 and = 0.04. As would be expected for a combination where = near zero, this monomer pair has a strong tendency toward alternation. The degree of alternation of the two monomers increases as the composition of the polymer approaches the 50/50 molar ratio that alternation dictates (5,6). Another complicating factor in defining chemical stmcture is the fact that butadiene can enter the polymer chains in the cis (1), trans (2), or vinyl(l,2) (3) configuration ... 

The preparation and characterization of 1,3-butadiene monomer is discussed extensively elsewhere (1 4) (see Butadiene). Butadiene monomer can be purified by a variety of techniques. The technique used depends on the source of the butadiene and on the polymerization technique to be employed. Emulsion polymerization, which is used to make amorphous /n j -l,4-polybutadiene (75% trans-1 4 , 5% kj -l,4 20% 1,2), is unaffected by impurities during polymerization. However, both anionic and Ziegler polymerizations, which are used to prepare kj -l,4-polybutadiene, mixed cis-1 4 and... 

The Ekestone group also polymerized 1,3-butadiene to give an extremely high mol wt polybutadiene of 70% cis-1 4 stmcture. In thek research, they purposefully avoided the preparation of vinyl stmctures in both polyisoprene and polybutadiene since it was beheved that vinyl groups adversely affected tke performance. Since natural mbber was 99.9% cis-1 4 stmcture and had superior properties, they beheved that a 1,4 stmcture was necessary for acceptable physical properties. The addition of polar compounds to the hthium-catalyzed polymerization of butadiene changes the microstmcture from the 90% tij -l,4 stmcture to a mixed cis-1 4 and trans-1 4 microstmcture. 

Polymerization temperature, °C trans 1,4 Addition inverted cis 1,2 Addition Isomerized 1,2 3,4 Addition... 

The chemical structure of SBR is given in Fig. 4. Because butadiene has two carbon-carbon double bonds, 1,2 and 1,4 addition reactions can be produced. The 1,2 addition provides a pendant vinyl group on the copolymer chain, leading to an increase in Tg. The 1,4 addition may occur in cis or trans. In free radical emulsion polymerization, the cis to trans ratio can be varied by changing the temperature (at low temperature, the trans form is favoured), and about 20% of the vinyl pendant group remains in both isomers. In solution polymerization the pendant vinyl group can be varied from 10 to 90% by choosing the adequate solvent and catalyst system. 

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