Green light LED activated ligation of a scalable, versatile chalcone chromophore

Literature Information

Publication Date 2021-06-21
DOI 10.1039/D1PY00533B
Impact Factor 5.582
Authors

Kevin De Bruycker, Aaron S. Micallef


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Abstract

Herein we introduce a photoreactive chalcone moiety that can be synthesized at a scale of several grams with ease, and efficiently undergoes a [2 + 2] photocycloaddition with light up to just below 500 nm as determined by an action plot. The peak chalcone reactivity is at 440 nm which is red-shifted by 25 nm compared to the absorption maximum at 415 nm. The chalcone was attached to a RAFT agent enabling reversible deactivation radical polymerization. The resulting polymer subsequently took part in a photoligation triggered by light from an LED centered at 505 nm. Thus, we introduce a chalcone that is capable of overcoming the synthetic disadvantages associated with styrylpyrenes and can readily undergo [2 + 2] photocycloadditon with visibile light.

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