4.7 Article

Conformational Steering in Substituted Poly(3,6-phenanthrene)s: A Linear and Nonlinear Optical Study

Journal

MACROMOLECULES
Volume 42, Issue 12, Pages 4282-4287

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ma900447x

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Funding

  1. Katholieke Universiteit Leuven (GOA)
  2. Scientific Research (FWOVlaanderen)
  3. Scientific Research (FWO-Vlaanderen)

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The synthesis of a chiral, 9, 10-dialkoxy-functionalized poly(3,6-phenanthrene) and the study of its chiroptical properties in different solvents is reported. The polymer was prepared by a Suzuki cross-coupling reaction. UV-vis, circular dichroism, and fluorescence spectroscopy and hyper-Rayleigh scattering were used to demonstrate that this polymer adopts a random coil conformation in a good solvent and folds into a one-handed helical conformation in poor solvents rather than stacking in a chiral way. Hyper-Rayleigh scattering proved to be a powerful tool for the investigation of the conformation of conjugated polymers because its response strongly depends on the conformation of the polymer.

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