AI Article Synopsis

  • The study investigates the structure and behavior of a semirigid conjugated polymer (DP10-PPV) in chloroform and toluene using various scattering techniques.
  • In chloroform, the polymer adopts a more extended conformation with higher values for radius of gyration, persistence length, and second virial coefficient, whereas toluene leads to significant clustering into microgels.
  • Compared to a similar polymer with shorter side chains, the aggregates formed in toluene are weaker and more easily disrupted due to less pi-pi interaction caused by the longer decyl side chains.

Article Abstract

The conformational structure and the interchain aggregation behavior of a semirigid conjugated polymer bearing a decyl side chain, poly(2,3-diphenyl-5-decyl-1,4-phenylenevinylene) (DP10-PPV), in solutions with chloroform and toluene have been investigated by means of small-angle neutron scattering (SANS), static light scattering (SLS) and dynamic light scattering (DLS). The radius of gyration, persistence length, and the second virial coefficient of the polymer in dilute solution as determined by SLS were higher in chloroform than in toluene; consequently, the polymer assumed a more extended wormlike chain conformation in the former. The difference in the strength of interaction in the two solvents gave rise to contrasting aggregation behavior of the polymer in the semidilute regime. While only a minor fraction of the polymer underwent segmental association in chloroform, a considerable fraction of it formed clusters (microgels) with several micrometers in size in toluene. These clusters were further found to consist of sheetlike nanodomains. Compared with the DP-PPV bearing a shorter hexyl side chain, DP6-PPV, the aggregates of DP10-PPV in toluene were weaker as they could be easily disrupted by moderate heating. This was attributed to a lack of strong pi-pi interaction between the DP10-PPV segments due to the greater steric hindrance imposed by the longer decyl side chains.

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http://dx.doi.org/10.1021/la803339fDOI Listing

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