Kume Shoko, Nishihara Hiroshi
Department of Chemistry, School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Dalton Trans. 2008 Jul 7(25):3260-71. doi: 10.1039/b716947g. Epub 2008 Mar 27.
The frontiers of novel photoresponsive materials constructed with photochromes and transition metal complexes are surveyed in this review. Strategies to develop new photofunctions are categorized into four types. In the first category, intramolecular electronic interactions between photochromes and metal complexes produce entangled responses such as redox-regulated photochromic reactions or tristable photochromism. In the second, light-induced molecular structural rearrangements of photochromes induce the transformation of flexible and labile coordination structures, which can be applied to complex photomechanics or photoelectron conversion. In the third, the photochromic moiety also acts as a photonic switch, transmitting a metal-metal interaction when it is located between two metal complex moieties. The last category concerns the development of new photochromic reactions, involving metal-ligand bond rearrangements. These reactions potentially induce drastic electronic tuning of the metal center, and can be used to develop light-driven molecular machines.
本综述探讨了由光致变色化合物和过渡金属配合物构建的新型光响应材料的前沿领域。开发新光功能的策略可分为四类。第一类,光致变色化合物与金属配合物之间的分子内电子相互作用产生纠缠响应,如氧化还原调节的光致变色反应或三稳态光致变色。第二类,光致变色化合物的光诱导分子结构重排会引起柔性和不稳定配位结构的转变,这可应用于复杂的光机械学或光电子转换。第三类,光致变色部分还充当光子开关,当它位于两个金属配合物部分之间时传递金属-金属相互作用。最后一类涉及新光致变色反应的开发,包括金属-配体键重排。这些反应可能会引起金属中心的剧烈电子调谐,并可用于开发光驱动分子机器。