2000
DOI: 10.1023/a:1026647529510
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Cited by 18 publications
(12 citation statements)
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“…In the case of PPyNSA, the yield decreases with d/m as follows: 0.8 > 0.1 > 0.5. This trend indicates that an optimal pH range of about 1.0 to 1.5 is required for the synthesis of the various PPys which agrees with Yakovleva [11] report that agitating the dopant and monomer mixture at a pH less than 1.0 dramatically decreased the rate of electrosynthesis of PPys [11]. Polypyrrole yield increased with the size of the dopant ion: b-naphthalene sulfonate giving higher yield than chloride.…”
Section: Polymerization Yieldsupporting
confidence: 83%
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“…In the case of PPyNSA, the yield decreases with d/m as follows: 0.8 > 0.1 > 0.5. This trend indicates that an optimal pH range of about 1.0 to 1.5 is required for the synthesis of the various PPys which agrees with Yakovleva [11] report that agitating the dopant and monomer mixture at a pH less than 1.0 dramatically decreased the rate of electrosynthesis of PPys [11]. Polypyrrole yield increased with the size of the dopant ion: b-naphthalene sulfonate giving higher yield than chloride.…”
Section: Polymerization Yieldsupporting
confidence: 83%
“…Similarly, the C-H stretching band at 3100 cm À1 was absent in all the three oxidized PPys, though there was a new sharp and pronounced peak at 3190 cm . In proposing a mechanism for the polymerization of polypyrrole in aqueous medium, Yakovleva [11] predicted the possibility of the formation of pyrrole complexes in acid solutions with the proton and anion in solution, in accordance with Scheme 2. He opined that the discharge of pyrrole complexes with the anion and proton and their destruction yield radical-cation and radical species which could jointly interact with the active ends of pyrrole links to induce the growth and development of polymer chains.…”
Section: Uv-vis Absorption and Solubilitymentioning
confidence: 85%
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“…Surfactants are used as polymer additives in order to control the morphology and when implicitly incorporated into the conducting polymer backbone, it serves to improve the conductivity, stability, solubility in organic solvents and processability [22]. Surfactants affect the preparation of conducting polymers in three ways, i.e., (i) the micelles control the distribution of reactants between the micellar and the aqueous phase and thus exerts some control over the polymerization pathway (ii) anionic surfactants may act as counter ions for the polymer polycations and (iii) the hydrophobic tail of the surfactant may adsorb on the polymer formed at the electrode surface and thus becomes part of the resulting material, influencing its chemical properties [23].…”
Section: Introductionmentioning
confidence: 99%
“…Conducting polymers have been a hot research area for many academic institutions for several decades . This research has supported the industrial development of conducting polymer products and has provided the fundamental understanding of the chemistry, physics and materials science of these materials.…”
Section: Introductionmentioning
confidence: 99%