Sulfonation of poly(p-phenylenediamine) polymer

References

• Benavente, J., Garcı́a, J. M., Riley, R., Lozano, A. E., & de Abajo, J. (2000). Sulfonated poly(ether ether sulfones): Characterization and study of dielectrical properties by impedance spectroscopy. Journal of Membrane Science, 175, 43–52.10.1016/S0376-7388(00)00395-1
   Web of Science ®Google Scholar
• Cataldo, F. (1996). On the polymerization of p-phenylenediamine. European Polymer Journal, 32, 43–50.10.1016/0014-3057(95)00118-2
   Web of Science ®Google Scholar
• Drioli, E., Regina, A., Casciola, M., Oliveti, A., Trotta, F., & Massari, T. (2004). Sulfonated PEEK-WC membranes for possible fuel cell applications. Journal of Membrane Science, 228, 139–148.10.1016/j.memsci.2003.07.023
   Web of Science ®Google Scholar
• Genies, C., Mercier, R., Sillion, B., Cornet, N., Gebel, G., & Pineri, M. (2001). Soluble sulfonated naphthalenic polyimides as materials for proton exchange membranes. Polymer, 42, 359–373.10.1016/S0032-3861(00)00384-0
   Web of Science ®Google Scholar
• Gil, M., Ji, X., Li, X., Na, H., Hampsey, J. E., & Lu, Y. (2004). Direct synthesis of sulfonated aromatic poly(ether ether ketone) proton exchange membranes for fuel cell applications. Journal of Membrane Science, 234, 75–81.10.1016/j.memsci.2003.12.021
   Web of Science ®Google Scholar
• Huang, M.-R., Ding, Y.-B., Li, X.-G., Liu, Y.-J., Xi, K., Gao, C.-L., & Kumar, R. V. (2014). Synthesis of semiconducting polymer microparticles as solid ionophore with abundant complexing sites for long-life Pb(II) sensors. ACS Applied Materials & Interfaces, 6, 22096–22107.10.1021/am505463f
   PubMed Web of Science ®Google Scholar
• Huang, M.-R., Lu, H.-J., & Li, X.-G. (2012). Synthesis and strong heavy-metal ion sorption of copolymer microparticles from phenylenediamine and its sulfonate. Journal of Materials Chemistry, 22, 17685–17699.10.1039/c2jm32361c
   Web of Science ®Google Scholar
• Lee, R.-H., Lai, H.-H., Wang, J.-J., Jeng, R.-J., & Lin, J.-J. (2008). Self-doping effects on the morphology, electrochemical and conductivity properties of self-assembled polyanilines. Thin Solid Films, 517, 500–505.10.1016/j.tsf.2008.06.079
   Web of Science ®Google Scholar
• Li, X.-G., Huang, M.-R., & Yang, Y.-L. (2001). Synthesis and characterization of o-phenylenediamine and xylidine copolymers. Polymer, 42, 4099–4107.10.1016/S0032-3861(00)00661-3
   Web of Science ®Google Scholar
• Li, X.-G., Huang, M.-R., Chen, R.-F., Jin, Y., & Yang, Y.-L. (2001). Preparation and characterization of poly(p-phenylenediamine-co-xylidine). Journal of Applied Polymer Science, 81, 3107–3116.10.1002/(ISSN)1097-4628
   Web of Science ®Google Scholar
• Li, X.-G., Huang, M.-R., Duan, W., & Yang, Y.-L. (2002). Novel multifunctional polymers from aromatic diamines by oxidative polymerizations. Chemical Reviews, 102, 2925–3030.10.1021/cr010423z
   PubMed Web of Science ®Google Scholar
• Mav, I., Zigon, M., Sebenik, A., & Vohlidal, J. (2000). Sulfonated polyanilines prepared by copolymerization of 3-aminobenzenesulfonic acid and aniline: The effect of reaction conditions on polymer properties. Journal of Polymer Science Part A: Polymer Chemistry, 38, 3390–3398.10.1002/(ISSN)1099-0518
   Web of Science ®Google Scholar
• Mav-Golež, I., Pahovnik, D., Bláha, M., Žigon, M., & Vohlídal, J. (2011). Copolymers of 2-methoxyaniline with 2- and 3-aminobenzenesulfonic and 2- and 3-aminobenzoic acids: Relationships between the polymerization conditions, structure, spectroscopic characteristics and conductivity. Synthetic Metals, 161, 1845–1855.10.1016/j.synthmet.2011.06.023
   Web of Science ®Google Scholar
• Nolte, R., Ledjeff, K., Bauer, M., & Mülhaupt, R. (1993). Partially sulfonated poly(arylene ether sulfone) – A versatile proton conducting membrane material for modern energy conversion technologies. Journal of Membrane Science, 83, 211–220.10.1016/0376-7388(93)85268-2
   Web of Science ®Google Scholar
• Pradeep, S., Arunraj, L., & Dhatchinamurthy, L. (2014). Synthesis and characterization of poly m-amino benzene sulfonic acid for sensor applications. Journal of NanoScience and NanoTechnology, 2, 390–393.
   Google Scholar
• Qi, Z., & Pickup, P. G. (1998). High performance conducting polymer supported oxygen reduction catalysts. Chemical Communications, 21, 2299–2300.10.1039/a805322g
   Web of Science ®Google Scholar
• Qi, Z., Lefebvre, M., & Pickup, P. G. (1998). Electron and proton transport in gas diffusion electrodes containing electronically conductive proton-exchange polymers. Journal of Electroanalytical Chemistry, 459, 9–14.10.1016/S0022-0728(98)00241-1
   Web of Science ®Google Scholar
• Ramkumar, R., & Minakshi, M. (2015). Fabrication of ultrathin CoMoO4 nanosheets modified with chitosan and their improved performance in energy storage device. Dalton Transactions, 44, 6158–6168.10.1039/C5DT00622H
   PubMed Web of Science ®Google Scholar
• Ramkumar, R., & Sundaram, M. M. (2016). A biopolymer gel-decorated cobalt molybdate nanowafer: Effective graft polymer cross-linked with an organic acid for better energy storage. New Journal of Chemistry, 40, 2863–2877.10.1039/C5NJ02799C
   Web of Science ®Google Scholar
• Rikukawa, M., & Sanui, K. (2000). Proton-conducting polymer electrolyte membranes based on hydrocarbon polymers. Progress in Polymer Science, 25, 1463–1502.10.1016/S0079-6700(00)00032-0
   Web of Science ®Google Scholar
• Tsuchida, E., Kaneko, M., & Kurimura, Y. (1970). Oxidative polymerization of aromatic amines in aqueous solution of iron chelate. Macromolecular Chemistry and Physics, 132, 209–213.10.1002/macp.1970.021320119
   Google Scholar