| Literature DB >> 33972556 |
Jiabin Yao1, Wanhua Wu2, Chao Xiao1, Dan Su1, Zhihui Zhong1, Tadashi Mori3, Cheng Yang4.
Abstract
Stimuli-responsive intelligent molecular machines/devices are of current research interest due to their potential application in minimized devices. Constructing molecular machines/devices capable of accomplishing complex missions is challenging, demanding coalescence of various functions into one molecule. Here we report the construction of intelligent molecular chiroptical photoswitches based on azobenzene-fused bicyclic pillar[n]arene derivatives, which we defined as molecular universal joints (MUJs). The Z/E photoisomerization of the azobenzene moiety of MUJs induces rolling in/out conformational switching of the azobenzene-bearing side-ring and consequently leads to planar chirality switching of MUJs. Meanwhile, temperature variation was demonstrated to also cause conformational/chiroptical inversion due to the significant entropy change during the ring-flipping. As a result, photo-induced chiroptical switching could be prohibited when the temperature exceeded an upper limit, demonstrating an intelligent molecular photoswitch having over-temperature protection function, which is in stark contrast to the low-temperature-gating effect commonly encountered.Entities:
Year: 2021 PMID: 33972556 DOI: 10.1038/s41467-021-22880-z
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919