Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United States.
Department of Chemistry, Fudan University, Shanghai 200433, China.
J Am Chem Soc. 2020 Jun 10;142(23):10308-10313. doi: 10.1021/jacs.0c04029. Epub 2020 May 28.
The assembly of a kinetically trapped daisy chain polymer under redox control has been achieved with a self-complementary monomer using an energy ratchet mechanism. The monomer is composed of a molecular pump at one end and a cyclobis(paraquat--phenylene) (CBPQT) ring at the other end. The pump and ring are linked together by a long collecting chain. When the monomer is reduced to its radical state, it self-assembles into a supramolecular daisy chain polymer on account of radical-pairing interactions. When all of the bipyridinium radical cations are quickly oxidized to dications, the CBPQT rings are forced to thread onto the collecting chains, forming an out-of-equilibrium, kinetically trapped daisy chain polymer. This polymer can be switched reversibly back to the supramolecular polymer by reduction, followed by depolymerization to afford the monomer as a result of slow oxidation. This proof-of-concept investigation opens up opportunities for synthesizing mechanically interlocked polymers using molecular machines.
在氧化还原控制下,通过使用自互补单体和能量棘轮机制,实现了动力学捕获的雏菊花链聚合物的组装。该单体由分子泵在一端和环双(对亚甲基-苯撑)(CBPQT)环在另一端组成。泵和环通过长收集链连接在一起。当单体还原为自由基状态时,由于自由基对相互作用,它自组装成超分子雏菊花链聚合物。当所有的联吡啶自由基阳离子迅速氧化为二阳离子时,CBPQT 环被迫穿入收集链,形成非平衡的、动力学捕获的雏菊花链聚合物。通过还原,该聚合物可以可逆地切换回超分子聚合物,随后由于缓慢氧化而解聚,得到单体。这一概念验证研究为使用分子机器合成机械互锁聚合物开辟了机会。