Control of the Switching Speed of Photochromic Naphthopyrans through Restriction of Double Bond Isomerization.

An efficient synthesis of photochromic fused-naphthopyrans was developed. UV-vis or sunlight irradiation of these uncolored compounds in solution led to the formation of a single colored photoisomer along with an unusual and uncolored bicyclic compound formed through an intramolecular photochemical Diels-Alder reaction. Both species faded thermally in the dark to the initial form. A mechanism for this transformation is proposed based on NMR studies of irradiated solutions. The new fused-naphthopyrans have been incorporated into hybrid organic-inorganic matrices affording light-yellow materials that develop intense red colorations under UV light and return to the initial uncolored state in just a few seconds, in the dark, at room temperature. These results are useful for the development of fast switching materials used in the production of photochromic lenses.