2009
DOI: 10.1515/epoly.2009.9.1.585
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Characterization of thin films of regioregular poly(alkylthiophene)s bearing optically active substituents

Abstract: Abstract:The spectroscopic behavior of thin films of regioregular poly(alkylthiophene)s bearing an optically active alkyl group has been investigated in the solid state under different sample preparation procedures. The experimental results are interpreted in terms of influence of the side-chain substituents on the extent of planarity of the polymeric chains and the formation of optically active chiral aggregates.

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“…Catellani, Abbate, and co-workers investigated solution and solid-state aggregates of several regioregular poly­(3-alkylthiophene)­s with optically active substituents. , Interestingly enough, by applying exciton theory formulas in combination with X-ray geometrical data, they were able to extract very reasonable estimates of interchain twist angles from the measured g abs values. Later on, the same group studied the impact of solvent dipping for improving the ECD response in spin-coated films of chiral poly­(3-alkylthiophene)­s, highlighting the impact of the film preparation procedure on the packing of the side chains and the planarity of the main chains. , Very recently, Swager and co-workers studied the ECD properties in thin films of chiral poly­(3-alkylsulfone)­thiophenes with main-chain helicity to explore a possible application in magneto-optic devices: interestingly, freshly prepared spin-coated samples revealed a helically ordered supramolecular structure, very similar to the solution phase one; instead, after thermal annealing at 150 °C a totally different ECD response was found, arising from a chiral structure with opposite helicity which is thermodynamically favored . It is important to stress that the ECD spectra of chiral PTs with main-chain helicity are very different from those of most common PTs, which are substantially planar and exhibit instead supramolecular (or interchain) chirality.…”
Section: Ecd Properties In Thin Films Of π-Conjugated Systems: Litera...mentioning
confidence: 99%
“…Catellani, Abbate, and co-workers investigated solution and solid-state aggregates of several regioregular poly­(3-alkylthiophene)­s with optically active substituents. , Interestingly enough, by applying exciton theory formulas in combination with X-ray geometrical data, they were able to extract very reasonable estimates of interchain twist angles from the measured g abs values. Later on, the same group studied the impact of solvent dipping for improving the ECD response in spin-coated films of chiral poly­(3-alkylthiophene)­s, highlighting the impact of the film preparation procedure on the packing of the side chains and the planarity of the main chains. , Very recently, Swager and co-workers studied the ECD properties in thin films of chiral poly­(3-alkylsulfone)­thiophenes with main-chain helicity to explore a possible application in magneto-optic devices: interestingly, freshly prepared spin-coated samples revealed a helically ordered supramolecular structure, very similar to the solution phase one; instead, after thermal annealing at 150 °C a totally different ECD response was found, arising from a chiral structure with opposite helicity which is thermodynamically favored . It is important to stress that the ECD spectra of chiral PTs with main-chain helicity are very different from those of most common PTs, which are substantially planar and exhibit instead supramolecular (or interchain) chirality.…”
Section: Ecd Properties In Thin Films Of π-Conjugated Systems: Litera...mentioning
confidence: 99%