Synthesis and Photochromism of 2H‐Naphthopyrans With an Extended Conjugation Skeleton

A new type of 2H-naphthopyran derivatives─benzonaphthopyrans (BNP) and naphthonaphthopyran (NNP)─have been synthesized, and their photochromic properties have been investigated in detail. We discovered that the extended conjugation skeleton could significantly improve the photochromic properties.

Abstract

Two series of new 2H-naphthopyran derivatives with an extended conjugation skeleton—benzonaphthopyrans (BNPs) and naphthonaphthopyran (NNPs)—have been designed and synthesized in this work. Their photochromic properties in organic solution and in poly(methyl methacrylate) (PMMA) have been investigated with special attention on the relationship between the extended conjugation skeleton and the photochromism. Compared to the simple benzopyran (BP) and the parent 2H-naphthopyran (NP), both BNPs and NNPs exhibit much better photochromic properties, such as faster photo-responsive and thermal fading rates, and excellent fatigue resistance, which indicates the extended conjugation skeleton can significantly improve the photochromic properties of 2H-naphthopyran derivatives. This is a new strategy to develop photochromic 2H-naphthopyrans with potential applications in fields such as ophthalmic lenses and photo-information storage.

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