Photocontrollable induction of supramolecular chirality in achiral side chain Azo-containing polymers through preferential chiral solvation‡
文献信息
Shunqin Jiang, Yin Zhao, Laibing Wang, Lu Yin, Zhengbiao Zhang, Jian Zhu, Wei Zhang, Xiulin Zhu
Here we designed a trans–cis photoisomerizable achiral side chain azobenzene-containing polymer, poly(6-[4-(4-methoxyphenylazo) phenoxy] hexyl methacrylate) (PAzoMA), to investigate the possibility of transferring chirality of chiral solvent molecules to polymers. Preferred chirality in supramolecularly assembled trans-azobenzene units of PAzoMA is successfully induced by limonene chirality. This chiral solvation induced chirality arises from superstructural chirality of well-assembled achiral azobenzene units in polymer side chains. The intense bisignated circular dichroism (CD) signals in the UV-vis region disappeared when trans–cis photoisomerization of PAzoMA occurred with 365 nm light irradiation. The polymer aggregate solution shows the CD-silent state when the cis-PAzoMA solution is subjected to 436 nm light irradiation. The intense CD signals with a ∼40 nm red-shift were recovered by heating the polymer aggregate solution to 60 °C and keeping it at this temperature for 40 min, then cooling it down to room temperature. The successful construction of a reversible chiral–achiral switch based on an achiral azobenzene-containing side chain polymer will open a new approach for production of chiroptical materials.
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Polymer Chemistry

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