Department of Chemistry, School of Science and Engineering, Aoyama Gakuin University, 5-10-1 Fuchinobe, Chuo-ku, Sagamihara, Kanagawa, 252-5258, Japan.
Adv Mater. 2019 Jan;31(2):e1805661. doi: 10.1002/adma.201805661. Epub 2018 Oct 31.
Photofunctional compounds have emerged as critically important materials for both fundamental studies and industrial applications. Control of the thermal decoloration speed to within several seconds while sustaining satisfactory photochromic colorability is an important challenge for the application of such materials to photochromic lenses and smart windows. Photochromic naphthopyran derivatives are utilized for photochromic lenses because of their high durability and easily controllable colorability. However, the residual color imparted by the long-lived transient species upon ceasing light irradiation remains a hindrance to practical applications. In this study, a strategy is demonstrated for on-demand control of the thermal decoloration speed of the transient colored species of naphthopyran derivatives. The increase in the ring-size of the alkylenedioxy moiety on the naphthopyrans accelerates the thermal back-reaction independently of the maximum-absorption wavelength of the colored isomer, leading to the realization of yellow-, red-, and blue-photochromic naphthopyrans with similar thermal fading speeds. This novel molecular design provides a strategy for the future development of advanced photoresponsive materials.
光功能化合物已成为基础研究和工业应用中至关重要的材料。控制热褪色速度在几秒钟内,同时保持令人满意的光致变色着色能力,是将这些材料应用于光致变色镜片和智能窗户的一个重要挑战。由于光致变色萘并吡喃衍生物具有高耐久性和易于控制的着色性,因此被用于光致变色镜片。然而,在停止光照后,由长寿命瞬态物种赋予的残余颜色仍然是实际应用的障碍。在这项研究中,展示了一种按需控制萘并吡喃衍生物的瞬态有色物种的热褪色速度的策略。在萘并吡喃上增加亚甲二氧基部分的环大小会独立于有色异构体的最大吸收波长加速热反,从而实现了黄色、红色和蓝色光致变色的萘并吡喃,它们具有相似的热褪色速度。这种新的分子设计为先进的光响应材料的未来发展提供了一种策略。