Li Anquan, Du Zhenglin, Zhang Shilong, Xie Jialin, Li Xia, Chen Qing, Tang Yisong, Chen Jiawen, Zhu Kelong
School of Chemistry, Sun Yat-Sen University Guangzhou 510275 China
School of South China Academy of Advanced Optoelectronics, South China Normal University Guangzhou 510006 China.
Chem Sci. 2024 Aug 13;15(36):14721-5. doi: 10.1039/d4sc04292a.
Here we present a compact and precise [2]catenane rotary motor that functions with a single recognition site, capable of achieving a 360° directional rotation powered by chemical fuels. The motor is propelled by an acid-base fueled benzimidazolium pumping cassette and deemed the smallest (molecular weight ∼ 994 Da) catenane rotary motor to date. It can effectively undergo a 180° rotation by transitioning the [24]crown-6 ether (24C6) from the benzimidazolium site to the less favorable alkyl moiety through sequential deprotonation, slipping, and re-protonation operations, generating a meta stable co-conformer. Subsequently, a discharging phase, triggered by de-benzylation and re-benzylation, facilitates the other half-rotation of the motor, returning the 24C6 to its initial position and completing the full directional rotation of the [2]catenane rotary motor within 18 hours. The precision of the motor's operation enables further advances in artificial molecular machines.
在此,我们展示了一种紧凑且精确的[2]连环烷旋转马达,它通过单一识别位点发挥作用,能够在化学燃料的驱动下实现360°定向旋转。该马达由酸碱驱动的苯并咪唑鎓泵送盒推动,被认为是迄今为止最小的(分子量约994 Da)连环烷旋转马达。通过连续的去质子化、滑动和再质子化操作,使[24]冠-6醚(24C6)从苯并咪唑鎓位点转移到较不利的烷基部分,它能够有效地进行180°旋转,产生一种亚稳共构象体。随后,由脱苄基化和再苄基化引发的放电阶段促进了马达的另一半旋转,使24C6回到其初始位置,并在18小时内完成[2]连环烷旋转马达的全定向旋转。该马达操作的精确性推动了人工分子机器的进一步发展。