Poly alkenes

Materials that typify thermoresponsive behavior are polyethylene—poly (ethylene glycol) copolymers that are used to functionalize the surfaces of polyethylene films (smart surfaces) (20). When the copolymer is immersed in water, the poly(ethylene glycol) functionaUties at the surfaces have solvation behavior similar to poly(ethylene glycol) itself. The abiUty to design a smart surface in these cases is based on the observed behavior of inverse temperature-dependent solubiUty of poly(alkene oxide)s in water. The behavior is used to produce surface-modified polymers that reversibly change their hydrophilicity and solvation with changes in temperatures. Similar behaviors have been observed as a function of changes in pH (21—24). [Pg.250]

Polyamides, poly(esters), poly(alkenes), PVC, polyurethanes, and rubbers... [Pg.123]

Poly(esters) and rubbers Poly(alkenes) and rubbers Cellulosic polymers, ethylene-vinyl acetate copolymers, poly(alkenes), PVC, rubbers, and poly(styrene) Cellulosic polymers, poly(esters), poly(alkenes), polyurethanes, PVC, rubbers, and poly(styrene)... [Pg.123]

Depending on the nature of the sulfur or phosphorus compound used, the product R2S = O or R3P = O may undergo a number of further reactions with ROOH groups, all of which convert the hydroperoxide group into an alcohol. These compounds tend to be only weakly effective so are generally used in conjunction with synergistic promoters. Suitable mixtures are used to stabilise a variety of polymers including poly(alkenes), ABS, and poly(stryrene). [Pg.125]

In contrast to the case of Cp2ZrX2/MAO giving atactic poly(alkene)s, Cp MCl2/MAO, M = Zr (139) and Hf (140), are the catalyst precursors of the syndiotactic polymerization of 1-butene and propylene [176]. Triad distribution indicated that this is chain-end controlled syndiospecific polymerization. The syndiospecificity is attributed to the increase of steric encumbrance around the metal center. Thus, Cp HfX2 is the most effective syndiospecific catalyst component in this system. [Pg.30]

In an extension of this work, the reuse of the polymeric catalyst was addressed and several new PE-poly(alkene) glycol copolymers were prepared [68]. Commercially available oxidized polyethylene (CO2H terminated, both high and low molecular weight) was converted to the acid chloride and reacted with Jeffamine D or Jeffamine EDR, and subsequently converted to the tributylammonium bromide salt with butyl bromide. These new quaternary salts were shown to catalyze the nucleophihc substitution of 1,6-dibromohexane with sodium cyanide or sodium iodide. While none of the polymeric quaternary salts catalyzed the reaction as well as tetrabutylammonium bromide, the temperature-dependent solubility of the polymers allowed removal of the polymer by simple filtration. [Pg.252]

An early commercial interest in poly (olefin sulfones) was sparked by the low raw materials cost, but this interest waned when it became apparent that thermal instability is a general characteristic of this class of materials. In 1970 Brown and O Donnell reported that poly (butene-1-sulfone) is degraded by gamma radiation with a G(s) approaching 10, making it one of the most radiation-sensitive polymers known (38-39). The potential for use of this radiation sensitivity in the design of electron beam resists was quickly realized by several members of the electronics industry. Bell Laboratories, RCA, and IBM published studies demonstrating the potential of poly (alkene... [Pg.126]

Poly(alkene sulfide)s are prepared by allowing the dihalide to drip slowly under vigorous stirring into a moderately concentrated aqueous polysulfide solu-... [Pg.304]

The development of smart catalysts is a relatively new field of investigation. One class of smart catalysts is based on homogeneous rhodium-based poly(alkene oxide)s, in particular those with a poly(ethylene oxide) backbone. Traditionally chemical-catalyzed reactions proceed in a manner in which the catalysts becomes more soluble and active as the temperature is raised. This can lead to exothermal runaways, thus, posing both safety and yield problems. These smart catalysts behave differently. As the temperature increases, they become less soluble, thus, precipitating out of solution and inactive. As the reaction mixture cools down, a smart catalysts redissolves and becomes active again (19). Other smart catalysts are being developed that dissociates at high temperatures (less active) and recombines at low temperatures (more active) (36). [Pg.252]

Despite its inherent difficulties, carbometallation has, in fact, played important roles in catalytic asymmetric carbon-carbonal bond formation. Isotactic and syndiotactic alkene polymerization involving both heterogeneous and homogeneous Ti and Zr catalysts must involve a series of face-selective carbometallation processes, although the main stereochemical concern in poly(alkene) formation is diastereoselectivity rather than enantioselectivity. This fascinating topic, however, is outside the scope of this chapter, and the readers are referred to Chapter 11 and other previous reviews [6]. [Pg.167]

The reaction of M3(CO)12 with both open-chain and cyclic poly-alkenes has attracted some attention, especially in the case of Ru3(CO)i2. In most of the examples reported, the organic fragment bonds to the metal framework in such a way as to interact with more than one of the three metal atoms (68-77). There are some exceptions to this general statement, however. One is the reaction of Ru3(CO)j 2 with cyclopentadiene, in which a mononuclear complex is obtained (78). In other cases, tetranuclear and hexanuclear compounds are obtained (79 81). Cluster breakdown has also been observed in the case of a rhodium complex upon reaction with ethylene (55) as shown in Fig. 3. [Pg.174]

Bergbreiter and co-workers have circumvented this problem of lower activity by complexing the rhodium salt on to poly(alkene oxide) oligomers (5.7) containing diphenylphosphine groups.213... [Pg.124]

Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...