Light- and Heat-Responsive Frustrated Lewis Pair Enables On-Demand Fixation of Ethylene
Frustrated Lewis pairs (FLPs) have been widely utilized as useful reagents and catalysts for activation of small molecules (SMs) through thermally controlled equilibrium formation of FLP-SM adducts. Herein, we report a light- and heat-responsive FLP system for on-demand fixation of ethylene. The system realizes capture and release of ethylene orthogonally triggered by visible light and heat, demonstrating potential utility as a nonmetallic and environmentally benign method for separation and storage of ethylene. The applicability to other alkenes is also demonstrated. Mechanistic investigations clarify that the photoexcited FLP enables stepwise radical addition to ethylene, followed by skeletal rearrangement to afford the FLP-ethylene adduct, which undergoes thermally promoted, concerted <i>retro</i>-cycloaddition to release ethylene and the free FLP. As a synthetic application, nonequilibrium, selective <i>cis</i>-to-<i>trans</i> isomerization of cyclooctene is achieved through the capture and release of cyclooctene with the FLP. This work discloses unique photochemical reactivity and application of FLPs, leading to further expansion of FLP chemistry into chemical science.
Authors
- Jun Takaya (ORCID: https://orcid.org/0000-0002-4582-2521)
- Taiki Yanagi
Institutions
- Tokyo Institute of Technology (JP)
- Institute of Science Tokyo (JP)
- The University of Osaka (JP)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2025-04-22
- DOI
- https://doi.org/10.1021/jacs.5c03130
- Citations
- 4
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 3.74
Funders
- Asahi Glass Foundation
- Sumitomo Foundation
- Ministry of Education, Culture, Sports, Science and Technology
- Tokuyama Science Foundation
- Nagase Science Technology Foundation