Helical conjugated polymers are of great interest for their potential as sources of circularly polarized luminescence for numerous electro-optical device applications including display technologies. Due to their relatively strong absorption cross sections and high emissivity in the visible wavelength range, these materials permit a detailed investigation of how the transition between helical and random coil forms are driven by polymer structural features such as chain length and chemical defects as well as environmental properties such as solvent and temperature. Bulk methods such as circular dichroism, absorption, and fluorescence as well as single-particle microscopy is used to probe the helix-to-coil phase transition in a model chiral polyfuran and to determine whether the conformations favored in solution are retained in the solid state. In addition, the transient dynamics and the effects of chemical doping on the electronic properties of the helix and coiled forms are explored.
Helical conjugated polymers are of great interest for their potential as sources of circularly polarized luminescence for numerous electro-optical device applications including display technologies. Due to their relatively strong absorption cross sections and high emissivity in the visible wavelength range, these materials permit a detailed investigation of how the transition between helical and random coil forms are driven by polymer structural features such as chain length and chemical defects as well as environmental properties such as solvent and temperature. Bulk methods such as temperature dependent absorption, emission, and circular dichroism as well as single-particle microscopy are used to probe the helix-to-coil phase transition in a model chiral polyfuran and to determine whether the conformations favored in solution are retained in the solid state. In addition, the transient dynamics and the effects of chemical doping on the electronic properties of the helix and coiled forms are explored.
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