Tuning the molecular properties of polybenzimidazole by copolymerization

dc.contributor.author Sannigrahi, Arindam
dc.contributor.author Arunbabu, Dhamodaran
dc.contributor.author Sankar, R. Murali
dc.contributor.author Jana, Tushar
dc.date.accessioned 2022-03-27T08:58:42Z
dc.date.available 2022-03-27T08:58:42Z
dc.date.issued 2007-10-25
dc.description.abstract In the present work, a series of novel random polybenzimidazole (PBI) copolymers consisting of m- and p-phenylene linkages are synthesized from various stoichiometric mixtures of isophthalic acid (IPA) and terephthalic acid (TPA) with 3,3′,4,4′-tetraaminobiphenyl (TAB) by solution copolycondensation in polyphosphoric acid (PPA). The resulting copolymers are characterized by different techniques to obtain their molecular properties parameters. The monomer concentration in the polymerization plays an important role in controlling the molecular weight of the polymer. Surprisingly, a simple change in the dicarboxylic acid architecture from meta (IPA) to para (TPA) increases the molecular weight of the copolymers, which is maximum for the para homopolymer. The low solubility of TPA in PPA is found to be the dominating factor for obtaining the higher molecular weight polymer in the case of the para structure. FT-IR study shows that the introduction of the para structure enhances the conjugation along the polymer chain. The positive deviation of the copolymer composition from the feed ratio is due to the higher reactivity ratio of TPA than IPA, which is obtained from proton NMR studies. The incorporation of the para structure in the chain enhances the thermal stability of the polymers. The para homopolymer shows 59 °C lower glass transition temperature compare to the meta homopolymer indicating enhancement of the flexibility of the polymer chain due the introduction of the p-phenylene linkage in the backbone. The Tg of the copolymers shows both positive and negative deviation from the expected Tg calculated by the Fox equation. The enhanced conjugation of the polymer chains also influences the photophysical properties of the polymers in solution. AU the PBI polymers exhibit strong fluorescence in dimethylacetamide solution. As expected, that all the polymers are amorphous in nature reveals that the copolymerization does not influence the packing characteristics of the PBI chains. © 2007 American Chemical Society.
dc.identifier.citation Journal of Physical Chemistry B. v.111(42)
dc.identifier.issn 15206106
dc.identifier.uri 10.1021/jp073973v
dc.identifier.uri https://pubs.acs.org/doi/10.1021/jp073973v
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12199
dc.title Tuning the molecular properties of polybenzimidazole by copolymerization
dc.type Journal. Article
dspace.entity.type
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