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Updated: Feb 3, 2026

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Wavelength-Controlled Dynamic Metathesis: A Light-Driven Exchange Reaction between Disulfide and Diselenide Bonds
Fuqiang Fan1,2, Shaobo Ji1, Chenxing Sun1
1Key Lab of Organic Optoelectronics & Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing, 100084, China.
Abstract:
Wavelength-controlled dynamic processes are mostly based on light-triggered isomerization or the cleavage/formation of molecular connections. Control over dynamic metathesis reactions by different light wavelengths, which would be useful in controllable dynamic chemistry, has rarely been studied. Taking advantage of the different bond energies of disulfide and diselenide bonds, we have developed a wavelength-driven exchange reaction between disulfides and diselenides, which underwent metathesis under UV light to produce Se-S bonds. When irradiated with visible light, the Se-S bonds were reversed back to those of the original reactants. The conversion of the exchange depends on the wavelength of the incident light. This light-driven metathesis chemistry was also applied to tune the mechanical properties of polymer materials. The visible-light-induced reverse reaction was compatible with reductant-catalyzed disulfide/diselenide metathesis, and could be utilized to develop a dissipative system with light as the energy input.
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