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Urea-poly complex

White91 used a 1,3-butadiene-urea canal complex to produce all-trans- 1,4-poly butadiene. The complex is formed only at temperatures in the range — 55 °C to 25 °C and needs a small amount of methanol to be formed. [Pg.343]

Schmidt, G, Enkelmann, V., Westphal, U., Droscher, M., and Wegner, G. (1985) Preparation of urea-poly(tetrahydrofuran) complexes and their application for fractionation of oligomers, Colloid Polym. Sci. 263, 120-127. [Pg.71]

Figure 12 DSC thermogram of poly(e-caprolactone) (a) crystallized from solution (b) native polymer extracted from PEC-urea-inclusion complex (c) recrystallized from melt. Figure 12 DSC thermogram of poly(e-caprolactone) (a) crystallized from solution (b) native polymer extracted from PEC-urea-inclusion complex (c) recrystallized from melt.
Association Complexes. The unshared electron pairs of the ether oxygens, which give the polymer strong hydrogen bonding affinity, can also take part in association reactions with a variety of monomeric and polymeric electron acceptors (40,41). These include poly(acryhc acid), poly(methacryhc acid), copolymers of maleic and acryflc acids, tannic acid, naphthoHc and phenoHc compounds, as well as urea and thiourea (42—47). [Pg.342]

Bentley et al.m recently improved upon Julia s epoxidation reaction. By using urea-hydrogen peroxide complex as the oxidant, l,8-diazabicyclo[5,4,0]undec-7-ene (DBU) as the base and the Itsuno s immobilized poly-D-leucine (Figure 4.2) as the catalyst, the epoxidation of a, (3-unsaturated ketones was carried out in tetrahydrofuran solution. This process greatly reduces the time required when compared to the original reaction using the triphasic conditions. [Pg.56]

Series of various mono,- bi-, and poly-(thio)urea-functionalized (poly)saccha-rides have already been synthesized and studied for molecular recognition of, e.g., dimethyl and phenylphosphate as model compounds for monoanionic and polyanionic phosphate esters, respechvely [111]. Thiourea derivatives such as 195-197 were analyhcally identified to provide double hydrogen bonding mediated host-guest complexes of well-defined dimension and orientations and were also reported to serve as phosphate binders even in the hydrogen bonding environment of water (Figure 6.57) [111]. [Pg.317]

Figure 5.19 Homogenous polymer blend of 2,7-diamido-l,8-naphthyridine (DAN) functionalized polystyrene and urea of guanosine (UG) functionalized poly(butyl methacrylate) (14), based on the four-point complementary complex formation between DAN and UG. Figure 5.19 Homogenous polymer blend of 2,7-diamido-l,8-naphthyridine (DAN) functionalized polystyrene and urea of guanosine (UG) functionalized poly(butyl methacrylate) (14), based on the four-point complementary complex formation between DAN and UG.
ESR spectra, 511 Uranium(VI) complexes dioxoneocupferron, 512 Uranium hexaalkoxides physical properties, 347 Uranyl complexes cupferron, 512 formamide, 491 glycolic acid, 472 hexafluoroacetylacetone, 373, 377 photochemistry, 385 rearrangement, 384 maleic acid conformation, 467 neutral 1,3-diketones, 402 poly ketones, 399 Urea... [Pg.1102]

Poly(vinyl alcohol) is utilized as a component of starch-based adhesives.11121114 Other patents report the use of partially oxidized starch,1115 dextrins,1116 dextrins and urea,1117 borax,1118 boric acid,1119 and vinyl methyl ether-maleic acid copolymers.1120 Other patents indicate the use of poly (vinyl alcohol) with partially hydrolyzed poly(vinyl acetate),1121 nonhy-drolyzed poly(vinyl acetate),1122 and poly(vinyl chloride).1123 A few patents have reported such poly acrylic additives as poly (acrylic acid)1124 and its salts,1125 poly(acrylamide),1126 1127 A-methylacrylamide or poly(A-acryl-amide),1128 and polyethyleneimine.1129 Polystyrene has also been used,1130 as well as more complex copolymers such as a maleic acid monobutyl ester-methyl vinyl ether copolymer, together with dextrin and polyacrylamide),1131 carboxylated ethyl acrylate-styrene zinc salt copolymer,1132 ethylene-methyl acrylate-vinyl acetate copolymer,1133 vinyl acetate-vinyl pyr-rolidone copolymer,1134 and ethylene-vinyl acetate copolymer.1135 Some adhesives are compounded with SBR latex1136 1138 and phenol-formaldehyde resins.1139... [Pg.413]

Polymerization of CFE in urea at -80"C has a mild stereoregulating influence compared to bulk polymerization at 60 °C, although the spectra in Figure 2 show that both polymers are substantially atactic. Three major triad resonances can be discerned more readily in spectrum (b), and these are assigned to mm, mr, and rr stereosequences as shown simply by analogy with the poly(l,2-difluoroethene) assignments (14,15). At present we have no basis to make definitive assignments, but those indicated are at least consistent with the known syndiotactic bias exerted by urea on the polymerization of complexed vinyl monomers (10). [Pg.156]

Many other similar applications have been reported such as the electrochemical determination of electroinactive cationic medicines,313 determination of urea,314 uric acid,315 and application to glucose biosensors to decrease interference of ascorbate, urate, and acetaminophen.316 Enzyme immobilized membranes are also sensing membranes, e.g. urea responsive membranes, poly(carboxylic acid) membranes in which urease is immobilized,317 fructose responsive membranes, and polyion complex membranes in which fructose dehydrogenase is immobilized.318 Such applications will expand further in the future and contribute to human life. [Pg.278]


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See also in sourсe #XX -- [ Pg.211 , Pg.213 , Pg.216 , Pg.217 , Pg.218 ]




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