Abstract
A cascade reaction involving a base-promoted nucleophilic substitution reaction between
diketones and α-bromoacetophenone derivatives and the subsequent selective condensation–cyclization
was developed for the synthesis of 1,2-diaroyl benzofurans. 1,2-Diaroyl benzofurans
with different functional groups and structures exhibit reversible photochromic behaviors
in solution, solid state, and thin films with diverse colors, demonstrating a potential
application in the field of optical functional materials.
Key words
benzofuran - synthesis - cascade reaction - photochromism - reversibility