Chromism and molecular weight of polyaniline derivatives

Abstract

The striking solvatochromic shift observed in polyaniline derivatives correlates with two solvent polarity scales, donor number (DN) and hydrogen bond acceptor scale (Taft's β-scale). The large shift is caused by conformational changes in solution that result in dramatic differences in relative molecular weight values obtained by gel permeation chromatography (MW GPC) in different solvents. For example, for poly- o-toluidine base in the emeraldine oxidation state, a low transition energy solvent like NMP (excitonic transition, λ max 608 nm) yields a very high molecular weight value ( M w ∼ 15,000 g mol −1) whereas a high transition energy solvent like CHCl 3 (excitonic transition, λ max 570 nm) yields an absurdly low value ( M w ∼ 650 g mol −1). An absolute molecular weight value, M w ∼ 4700 g mol −1, was obtained for the first time using laser light scattering (MW LS) suggesting that CHCl 3 promotes a highly coiled chain conformation whereas NMP promotes a more expanded, rod-like conformation. A similar trend is observed for poly- o-toluidine base in the fully oxidized pernigraniline oxidation state (Pierels transition). This suggests that even though the Pierels and excitonic transitions have different molecular origins their conformation driven solvatochromic shifts trend in a similar fashion which is different from thermochromic trends reported in previous studies.