Characterization of reaction intermediate aggregates in aniline oxidative polymerization at low proton concentration

Ding, Z; Sanchez, T; Labouriau, A; Iyer, S; Larson, T; Currier, R; Zhao, Y; Yang, D

HERO ID

3539766

Reference Type

Journal Article

Year

2010

Language

English

PMID

20701368

HERO ID 3539766
In Press No
Year 2010
Title Characterization of reaction intermediate aggregates in aniline oxidative polymerization at low proton concentration
Authors Ding, Z; Sanchez, T; Labouriau, A; Iyer, S; Larson, T; Currier, R; Zhao, Y; Yang, D
Journal Journal of Physical Chemistry B
Volume 114
Issue 32
Page Numbers 10337-10346
Abstract Aggregates of reaction intermediates form during the early stages of aniline oxidative polymerization whenever the initial mole ratio of proton concentration to aniline monomer concentration is low ([H(+)](0)/[An](0) <or= 1.0). Detailed characterization is carried out on those aggregates. The intermediate aggregates show a UV-Vis absorption peak at around 410 nm when dispersed in aqueous solution, whereas the peak is centered on 370 nm when dissolved in an organic solvent such as N-methylpyrrolidone. The electronic band gap decreases when the intermediates aggregate to form a solid, and thus, the absorption peak is red-shifted. Gel permeation chromatography (GPC) shows the aggregates contain a major low molecular weight peak with a long tail. The oligoanilines with low molecular weights consistently show a UV-Vis absorption peak at around 370 nm. Mass spectrometry confirms that the intermediate aggregates contain mainly a component with mass number 363 (M + H(+)), likely a tetramer. UV-Vis, GPC, mass spectrometry, NMR, FTIR, and XRD characterization results are presented and chemical structures for the tetramer are proposed. The major components of the intermediate aggregates are likely highly symmetric phenazine- and dihydrophenazine-containing structures. These particular organic compounds have not been identified before as intermediates. The aggregation and precipitation of the tetramers apparently stabilizes these intermediates. The aggregates are highly crystalline, as evidenced by powder X-ray diffraction. A new reaction mechanism for the formation of these intermediates is proposed.
Doi 10.1021/jp102623z
Pmid 20701368
Wosid WOS:000280727700011
Url <Go to ISI>://WOS:000280727700011
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English