Phenylenes hydrocarbons

In automotive and aerospace end uses, the apphcations ate also often electrical. Polysulfones do not have as good solvent resistance as poly(phenylene sulfide). They perform well in hydrocarbons like gasoline and oil, or in antifreeze, but ate attacked by the alcohol-blend fuel mixtures. This may limit their under-the-hood apphcations. 

Dendritic Poly(phenylene)s and Giant Polyaromatic Hydrocarbons (PAHs)... 

Cyclic enone, 12 185 Cyclic ethers, 10 567, 569 12 663 polymerization, 14 271 Cyclic fatigue, in ceramics, 5 633-634 Cyclic gas generators, 6 786-787, 789, 827 Cyclic halides, 19 56 Cyclic hexakis(thio-l,4-phenylene), melt polymerization of, 23 705 Cyclic hydrocarbons, 13 687 Cyclic hydroxyalkyl alkyl peroxide, 18 454 Cyclic ion exchange operation, 14 408-413 Cyclic ketones, 12 176, 177 14 590-592. See also Cyclic 1,2-diketones physical properties of, 14 591t hydroxyalkyl hydroperoxides from, 18 450... 

Membrane research is a rather diverse field, exploiting perfluorinated iono-mers, hydrocarbon and aromatic polymers, and acid-base polymer complexes. Polyether and polyketo polymers with statistically sulfonated phenylene groups such as sPEK, sPEEK, and sPEEKK or polymers on the basis of benzimidazole have been tested as well. Recent reviews on membrane synthesis and experimental characterization can be found in the literature. ... 

Fiereby, Vq refers to the maximal electronic coupling element and p is the decay coefficient factor (damping factor), which depends primarily on the nature of the bridging molecule. From the linear plot of In ETmax versus R the p value is obtained as 0.60 A [47]. This p value is located within the boundaries of nonadiabatic ET reactions for saturated hydrocarbon bridges (0.8-1.0 A ) and unsaturated phenylene bridges (0.4 A ) [1-4,54,55]. 

Fluoranthene (Called 1,2-benzo-acenaphthy-len or 1,8-o-phenylen-naphthylen in Ger), C16H10(Thought to be ClaH10in early literature), mw 202.24, colorless ndls, sp gr 1.158 at 20°, nD 1.739 at 20°, bp 393°, 217°(30mm Hg), mp 109.5-110.5°, sol In benz, chlf, eth, HAc hot ale. A tetracyclic fused ring aromatic hydrocarbon, this material is found in some coal tars. It forms definite complexes with many poly nitrated aromatics (Refs 1 to 6) Refs 1) Beil 5, 685, (340, 344), [609] 2276 2) J. vonBraun E. Anton, Ber... 

Polyacetylene and poly(p-phenylene) (PPP) are two polymeric hydrocarbons with a unique property both are conducting polymers on doping. Polyacetylene, a... 

The complexes [Cu(S2CNEt2]2] and [Cu S2P(OPr )2 2] have been shown to be extremely effective scavengers for peroxy radicals and can be used to inhibit the autoxidation of hydrocarbons.99 Poly(2,6-dimethyl-1,4-phenylene oxide) can be effectively stabilized against thermal degradation by the bistriazene complex (41).100 The stabilizing action is thought to involve quenching of thermally excited states and the decomposition of hydroperoxides by the complex. 

Poly[2-methoxy-5-(3, 7 -dimethyloctyloxy)]-l,4-phenylene vinylene Polycyclic aromatic hydrocarbon Poly(3,4-ethylenedioxythiophene)... 

The study of the photochemistry of aryl carbanions has been restricted to aryllithiums with only a limited number of studies available. Hence, a general picture of their photochemistry is not available at this time. Photolysis of phenyllithium in the presence of aromatic hydrocarbons such as naphthalene, biphenyl, phenylene, etc. in diethyl ether results in electron transfer from the phenyllithium to the aromatic hydrocarbon, with production of the corresponding hydrocarbon radical anion, as observed by ESR spectroscopy [6-8] (Eq. 1). Photolysis of phenyllithium or 2-naphthyllithium alone gave the corresponding biaryl products and metallic lithium [9-10]. For this reaction, it is possible to write a mechanism which does not require electron transfer from the anion [9,10],... 

Schulman, J. M. Disch, R. L. Properties of phenylene-based hydrocarbon bowls and archimedene, J. Phys. Chem. A 2005,109, 6947-6952. 

Cyclohydrogenation of poly(phenylene) dendrimers has to be mentioned as a special case of topochemical polymerization proceeding in solution. The reaction yielded extended polycyclic aromatic hydrocarbons containing up to 132 carbon atoms (Figure 17b) [188]. 

The target structures in the final example are fully aromatic polymeric hydrocarbons, consisting of all-carbon six-membered rings - so-called angularly annulated polyacenes 91 [55]. The structural difference between those and the methylene-bridged poly(phenylene)s is the replacement of the benzylic methylene bridges by vinylene moieties. 

Of other substances containing the furan ring in an otherwise hydrocarbon molecular environment, 5 forms an anion-radical on reduction with potassium. This radical has been the subject of a solution ESR and ENDOR study by Gerson and co-workers. Spin distribution, ion-pairing effects, and barriers to rotation of the phenylene groups were investigated. As implied earlier in the discussion of ECL, isobenzofurans and tetraphenylfuran also form anion-radicals. " ... 

FIGURE 9.4 Dependence of constants (a, b, and c present Henry constant, sorption affinity constant, and Langmuir sorption capacity respectively) of the model of dual-mode sorption of hydrocarbons by glassy polyphenylene oxides on boiling temperatures of hydrocarbons Z), is pDMePO, poly-2,6-dimethyl-l,4-phenylene oxide o is pDPhPO, poly-2,6-diphenyl-l,4-phenylene oxide is pDMePO/pDPhPO copolymer (97.5/2.5% mol) v is pDMePO/pDPhPO copolymer (75/25% mol). (From analysis of results presented in Lapkin, A.A., Roschupkina, O.P., and Ilinitch, O.M., J. Membr. Sci., 141, 223, 1998.)... 

Lapkin AA, Roschupkina OP, and Ilinitch OM. Transport of C —C3 hydrocarbons in poly(phenylene oxides) membranes. JMembr Sci 1998 141(2) 223-229. 

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