By altering solvent/nonsolvent ratio and temperature, a comprehensive study is carried out to understand the molecular aggregation of poly[(1,3-phenyleneethynylene)- alt -oligo(2,5-dialkoxy-1,4-phenyleneethynylene)]s 1 and 2 in solution, which possess different lengths of linear phenyleneethynylene (PE) fragments. Although both polymers exhibit random-coil conformation in THF solution, PPE 2 of longer rigid-rod fragment exhibits a higher tendency to form aggregate than 1 . In a good solvent, optical spectra of PPEs reveal a gradual spectral shift in responding to the temperature change, which is attributed to molecular conformational change (planarity of chromophore). With addition of methanol to polymer solutions in THF, UV−vis absorption spectroscopy detects the aggregation band from 2 but not from 1 . The combination of solvent/nonsolvent and low temperature provides improved sensitivity to probe molecular aggregation. Although chromophore planarity is anticipated to play an important role, current results favor the π−π interaction in the aggregate formation of 1 and 2 .
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Chu et al. (2003) studied this question.
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