Ikai Tomoyuki, Okubo Mitsuhiro, Wada Yuya
Graduate School of Natural Science and Technology , Kanazawa University , Kakuma-machi, Kanazawa 920-1192 , Japan.
Department of Molecular and Macromolecular Chemistry, Graduate School of Engineering , Nagoya University , Chikusa-ku, Nagoya 464-8603 , Japan.
J Am Chem Soc. 2020 Feb 12;142(6):3254-3261. doi: 10.1021/jacs.9b13584. Epub 2020 Feb 3.
We report the synthesis of one-dimensional supramolecular polymers composed of one-handed helical macromolecules bearing fluorescent pendant groups and the generation of circularly polarized light on the basis of hierarchical chiral amplification starting from a tiny amount of chiral substituent. Copolymerization of benzo[1,2-:4,5-']dithiophene-appended achiral/chiral isocyanides (99:1, mol/mol) with a solid-state photoluminescence feature afforded submicrometer supramolecular fibers, in which almost perfect single-handed helical polyisocyanides were noncovalently connected end to end. The resulting helical supramolecular polymers were further helically assembled to form a cholesteric liquid crystal film with an intense circularly polarized luminescence (CPL) signal. Surprisingly, the supramolecular system containing only 0.01 mol % of the chiral monomer unit also emitted the observable circularly polarized light owing to multiple chiral amplification from an infinitesimal point chirality to helical chirality and then to supramolecular chirality. Furthermore, chiral information was efficiently transferred from the helically assembled supramolecular system containing 1 mol % of the chiral unit to achiral dye molecules blended in the film, allowing full-color tunable induced CPL with luminescence dissymmetry factors greater than 1.0 × 10. This unprecedentedly strong chiral amplification enables the creation of helical supramolecular polymers and chirally assembled systems with various chiral functions based solely on an infinitesimal chiral source.
我们报道了由带有荧光侧基的单手螺旋大分子组成的一维超分子聚合物的合成,以及基于从微量手性取代基开始的分级手性放大产生圆偏振光。苯并[1,2-:4,5-']二噻吩连接的非手性/手性异氰化物(99:1,摩尔/摩尔)进行固态光致发光特征的共聚反应,得到了亚微米级的超分子纤维,其中几乎完美的单手螺旋聚异氰化物非共价地首尾相连。所得的螺旋超分子聚合物进一步螺旋组装形成具有强烈圆偏振发光(CPL)信号的胆甾相液晶膜。令人惊讶的是,仅含有0.01 mol%手性单体单元的超分子体系也由于从无限小的点手性到螺旋手性再到超分子手性的多重手性放大而发射出可观察到的圆偏振光。此外,手性信息从含有1 mol%手性单元的螺旋组装超分子体系有效地转移到膜中混合的非手性染料分子上,从而实现了发光不对称因子大于1.0×10的全色可调谐诱导CPL。这种前所未有的强手性放大使得仅基于无限小的手性源就能创建具有各种手性功能的螺旋超分子聚合物和手性组装体系。