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Poly[2(6)-aminoazulene]: synthesis, photophysical properties, and proton conductivity

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Abstract

Dimeric aminoazulene and poly[2(6)-aminoazulene] are synthesized by Buchwald–Hartwig coupling of the corresponding monomeric carbamatoaminozulenes followed by hydrolysis. The absorption maxima shift from 394 nm for monomeric aminoazulene to 481 nm for the dimer and 591 nm for the polymer. Protonation of the monomeric and polymeric aminoazulenes occurs exclusively at the C1 position(s). The λmax also shows a similar trend at 410, 492 and 670 nm for protonated monomeric, dimeric and polymeric aminoazulenes. These aminoazulenes undergo reversible protonation/deprotonation at the C1 position(s) and both forms exhibit extension of conjugation through amino moieties. Preliminary DFT calculations suggest that the C–N bonds are significantly shortened because of resonance contributions. By incorporating 3 wt% protonated polyaminoazulene in Nafion, the composite membrane has shown 50% reduction in methanol permeability with retention of proton conductivity and 3-fold increment in water permeability, which are advantageous for direct methanol fuel cell application.

Graphical abstract: Poly[2(6)-aminoazulene]: synthesis, photophysical properties, and proton conductivity

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Publication details

The article was received on 31 Jan 2017, accepted on 03 Mar 2017 and first published on 06 Mar 2017


Article type: Research Article
DOI: 10.1039/C7QO00087A
Citation: Org. Chem. Front., 2017, Advance Article
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    Poly[2(6)-aminoazulene]: synthesis, photophysical properties, and proton conductivity

    I. C. Hou, V. Shetti, S. Huang, K. Liu, C. Chao, S. Lin, Y. Lin, L. Chen and T. Luh, Org. Chem. Front., 2017, Advance Article , DOI: 10.1039/C7QO00087A

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