4.8 Article

Motorized Macrocycle: A Photo-responsive Host with Switchable and Stereoselective Guest Recognition

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 29, 页码 16129-16138

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202104285

关键词

capture and release; host-guest interactions; motorized macrocycles; photo-responsiveness; stereoselectivity

资金

  1. National Natural Science Foundation of China [22025503, 21790361, 21871084, 21672060]
  2. Shanghai Municipal Science and Technology Major Project [2018SHZDZX03]
  3. Fundamental Research Funds for the Central Universities
  4. Programme of Introducing Talents of Discipline to Universities [B16017]
  5. Program of Shanghai Academic/Technology Research Leader [19XD1421100]
  6. Shanghai Science and Technology Committee [17520750100]
  7. European Union's Horizon 2020 research and innovation programme under the Marie Skodowska Curie grant [101025041, 838280]
  8. European Research Council (ERC) [694345]
  9. Dutch Ministry of Education, Culture and Science (Gravitation program) [024.001.035]
  10. Marie Curie Actions (MSCA) [101025041] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

Designing photo-responsive host-guest systems using light-driven molecular motors can provide versatile tools for constructing smart systems and materials. The intramolecular cyclization of molecular motors enables the switchable chiral guest recognition, offering a reversible modulation of binding affinity and stereoselectivity in the host-guest interaction.
Designing photo-responsive host-guest systems can provide versatile supramolecular tools for constructing smart systems and materials. We designed photo-responsive macrocyclic hosts, modulated by light-driven molecular rotary motors enabling switchable chiral guest recognition. The intramolecular cyclization of the two arms of a first-generation molecular motor with flexible oligoethylene glycol chains of different lengths resulted in crown-ether-like macrocycles with intrinsic motor function. The octaethylene glycol linkage enables the successful unidirectional rotation of molecular motors, simultaneously allowing the 1:1 host-guest interaction with ammonium salt guests. The binding affinity and stereoselectivity of the motorized macrocycle can be reversibly modulated, owing to the multi-state light-driven switching of geometry and helicity of the molecular motors. This approach provides an attractive strategy to construct stimuli-responsive host-guest systems and dynamic materials.

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