2008
DOI: 10.1134/s1811238208010037
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Highly phenylated polyarylenes: Synthesis, properties, and applications

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Cited by 7 publications
(3 citation statements)
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“…Maximum values of 222 mS cm −1 and 268 mS cm −1 were observed at 95 % RH for sPPN‐H + at 30 °C and 80 °C, respectively. These values are significantly higher than previously reported sulfonated polyphenylenes and the 79 mS cm −1 (30 °C) and 113 mS cm −1 (80 °C) values obtained for Nafion NR‐211 under identical conditions. sPPB‐H + exhibits proton conductivities of 129 mS cm −1 and 172 mS cm −1 at 30 °C and 80 °C respectively, likewise larger than previously reported sPPP‐H + and NR‐211.…”
Section: Methodscontrasting
confidence: 64%
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“…Maximum values of 222 mS cm −1 and 268 mS cm −1 were observed at 95 % RH for sPPN‐H + at 30 °C and 80 °C, respectively. These values are significantly higher than previously reported sulfonated polyphenylenes and the 79 mS cm −1 (30 °C) and 113 mS cm −1 (80 °C) values obtained for Nafion NR‐211 under identical conditions. sPPB‐H + exhibits proton conductivities of 129 mS cm −1 and 172 mS cm −1 at 30 °C and 80 °C respectively, likewise larger than previously reported sPPP‐H + and NR‐211.…”
Section: Methodscontrasting
confidence: 64%
“…Proton conductivity measurements were performed using electrochemical impedance spectroscopy (EIS) under relative humidities (RH) ranging from 30 %to95%,atboth 30 8 8Cand 80 8 8C ( Figure 1). Maximum values of 222 mS cm À1 and 268 mS cm À1 were observed at 95 %R Hf or sPPN-H + at 30 8 8Ca nd 80 8 8C, respectively.T hese values are significantly higher than previously reported sulfonated polyphenylenes [20,24,[30][31][32] and the 79 mS cm À1 (30 8 8C) and 113 mS cm À1 (80 8 8C) values obtained for Nafion NR-211 under identical conditions. sPPB-H + exhibits proton conductivities of 129 mS cm À1 and 172 mS cm À1 at 30 8 8Cand 80 8 8Crespectively, likewise larger than previously reported sPPP-H + and NR- 211.…”
contrasting
confidence: 52%
“…The formation of a nanoporous structure in the case of supercritical СО 2 , along with introduc tion of fluorinated fragments, contributes to the cre ation of materials with very low dielectric constants (1.58-1.97) [148][149][150]. The Diels-Alder cycloaddi tion is one of the methods of obtaining these polymers [151]. This method is employed for the synthesis of both initial monomers and polymers [145,152].…”
Section: Carbochain Condensation Polymersmentioning
confidence: 99%