Department of Chemistry and Biological Science, College of Science and Engineering, Aoyama Gakuin University, 5-10-1 Fuchinobe, Chuo-ku, Sagamihara, Kanagawa 252-5258, Japan.
J Am Chem Soc. 2023 Feb 15;145(6):3318-3322. doi: 10.1021/jacs.2c13331. Epub 2023 Feb 7.
Selective bidirectional photoisomerization reactions with high conversion ratios between stable and metastable isomers by irradiation of photochromic molecules with visible light of different wavelengths have been an important issue for many years. For negative photochromic molecules known so far, metastable isomers also absorb UV or visible light in the same region as stable isomers, making it difficult to selectively achieve the reverse reaction by visible-light irradiation. We have demonstrated that the absorption bands of the stable and metastable isomers of 3-phenylperylenyl-bridged imidazole dimer are largely separated by more than 140 nm and that almost quantitative and selective bidirectional photoconversion can be achieved by 660 and 460 nm light. Furthermore, the forward reaction can be achieved completely with near-infrared light of 785 nm.
多年来,利用不同波长可见光辐照光致变色分子,实现稳定和亚稳态异构体之间高转化率的选择性双向光致异构反应一直是一个重要的问题。对于迄今为止已知的负光致变色分子,亚稳态异构体也在与稳定异构体相同的区域吸收紫外光或可见光,这使得通过可见光辐照难以选择性地实现逆反应。我们已经证明,3-苯基苝桥联咪唑二聚体的稳定和亚稳态异构体的吸收带通过 140nm 以上的波长分离,并且可以通过 660nm 和 460nm 的光实现几乎定量和选择性的双向光致转化。此外,近红外光 785nm 可以完全实现正向反应。