9-Aryl-phenalenones: Bioinspired thermally reversible photochromic compounds for photoswitching applications in the pico-to milliseconds range

Ultrafast photochromic molecules are being actively investigated to meet the demand for fast optical switching systems. Inspired on the irreversible cyclization of 9-phenylphenalenone plant metabolites to yield highly-coloured naphthoxanthenes for the purpose of defense against pathogens, aryl-substituted phenalenones have been developed that undergo a similar but reversible photochromic reaction. The lifetime of the naphthoxanthene photoisomer spans nine orders of magnitude, ranging from tens of picoseconds to tens of milliseconds depending on the electronic properties of the 9-aryl group.

Automated summary

Researchers have developed aryl-substituted phenalenones inspired by the irreversible cyclization of 9-phenylphenalenone plant metabolites to yield highly-colored naphthoxanthenes. The lifetime of the naphthoxanthene photoisomer ranges from tens of picoseconds to tens of milliseconds depending on the electronic properties of the 9-aryl group.