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.

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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

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article

Light- and Heat-Responsive Frustrated Lewis Pair Enables On-Demand Fixation of Ethylene

Jun Takaya, Taiki Yanagi
4 citations
Journal of the American Chemical Society
Organoboron and organosilicon chemistry
3.74
article

Light- and Heat-Responsive Frustrated Lewis Pair Enables On-Demand Fixation of Ethylene

Jun Takaya, Taiki Yanagi
article en
4 citations

Abstract

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.

Journal of the American Chemical SocietyVol. 147(18)
Tokyo Institute of Technology (JP), Institute of Science Tokyo (JP), The University of Osaka (JP)
Asahi Glass Foundation, Sumitomo Foundation, Ministry of Education, Culture, Sports, Science and Technology, Tokuyama Science Foundation, Nagase Science Technology Foundation
Openalex Percentile: Top 8%
Organoboron and organosilicon chemistry
3.74
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Light- and Heat-Responsive Frustrated Lewis Pair Enables On-Demand Fixation of Ethylene — Jun Takaya, Taiki Yanagi · Journal of the American Chemical Society (2025) | TGRS Research Map | TGRS