Department of Chemistry, University of Miami, Coral Gables, FL 33124, USA.
Chem Commun (Camb). 2022 Jun 8;58(46):6571-6585. doi: 10.1039/d2cc01758j.
Exerting control on excited state processes has been a long-held goal in photochemistry. One approach to achieve control has been to mimic biological systems in Nature (, photosynthesis) that has perfected it over millions of years by performing the reactions in highly organized assemblies such as membranes and proteins by restricting the freedom of reactants and directing them to pursue a select pathway. The duplication of this concept at a smaller scale in the laboratory involves the use of highly confined and organized assemblies as reaction containers. This article summarizes the studies in the author's laboratory using a synthetic, well-defined reaction container known as octa acid (OA). OA, unlike most commonly known cavitands, forms a capsule in water and remains closed during the lifetime of the excited states of included molecules. Thus, the described excited state chemistry occurs in a small space with hydrophobic characteristics. Examples where the photophysical and photochemical properties are dramatically altered, compared to that in organic solvents wherein the molecules are freely soluble, are presented to illustrate the value of a restricted environment in controlling the dynamics of molecules on an excited state surface. While the ground state complexation of the guest and host is controlled by well-known concepts of tight-fit, lock and key, complementarity, , free space around the guest is necessary for it to be able to undergo structural transformations in the excited state, where the time is short. This article highlights the role of free space during the dynamics of molecules within a confined, inflexible reaction cavity.
控制激发态过程一直是光化学的长期目标。一种实现控制的方法是模仿自然界中的生物系统(例如光合作用),这些系统通过在膜和蛋白质等高度组织的组装体中进行反应,限制反应物的自由度并引导它们选择特定的途径,从而在数百万年的时间里完善了这一过程。在实验室中以较小的规模复制这一概念涉及使用高度受限和组织良好的组装体作为反应容器。本文总结了作者实验室使用一种称为八酸(OA)的合成、明确定义的反应容器进行的研究。与大多数常见的空腔分子不同,OA 在水中形成胶囊,并且在包含分子的激发态的寿命期间保持关闭。因此,所描述的激发态化学在具有疏水性的小空间中发生。与分子在有机溶剂中自由溶解的情况相比,呈现了光物理和光化学性质发生显著变化的例子,说明了在控制分子在激发态表面上的动力学方面受限环境的价值。虽然客体和主体的基态络合受紧配合、锁和钥匙、互补性等众所周知的概念控制,但客体周围的自由空间对于它能够在时间短暂的激发态下进行结构转变是必要的。本文强调了在受限、不灵活的反应腔体内分子动力学过程中自由空间的作用。