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Polypara-phenylene

M. Dubois, A. Naji,J.P. Buisson, B. Humbert, E. Grivei, and D. Billaud, Characterisation of carbonaceous materials derived from polypara-phenylene pyrolyzed at low temperature, Carbon, 38(9) 1411-1417, 2000. [Pg.264]

The pristine conjugated polymers have been reported to contain electronic spins, presumably originating from inter-chain cross-linking in polyacetylene [25,26], formation of polynuclear structures in polypara-phenylene [27] and so on. The inter- and intra-chain reactions between these reactive sites can alter the chemical structure of conductive polymers even when they are pure, affecting their dopability and hence the electroactivity. [Pg.799]

J. L. Bredas, R. R. Chance, R. Silbey, Comparative theoretical study of the doping of conjugated polymers - polarons in polyacetylene and polypara-phenylene, Physical Review B 1982, 26, 5843. [Pg.310]

One major advantage of ion implantation is the control over the doping level, which, with the help of the fluence, we determine exactly [5]. The usual range is from lO to 10 ions/cm , which implies for polypara-phenylene KC6H4), density p =. 2 g/cm ] a doping level of 1-10% with regard to number of monomers or 0.1-1% with regard to total number of atoms. [Pg.589]


See other pages where Polypara-phenylene is mentioned: [Pg.85]    [Pg.766]    [Pg.848]    [Pg.871]    [Pg.232]    [Pg.71]    [Pg.85]    [Pg.766]    [Pg.848]    [Pg.871]    [Pg.232]    [Pg.71]    [Pg.411]    [Pg.432]    [Pg.418]    [Pg.466]    [Pg.3243]   
See also in sourсe #XX -- [ Pg.259 ]




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