Light-Controlled Functions with Metal–Organic Capsules: From Guest Release to Catalysis, Separation, and Molecular Transport

偶氮苯 分子开关 光异构化 化学 超分子化学 分子机器 纳米技术 分子 模板 分子工程 分子识别 锂(药物) 组合化学 离子 分子线 催化作用 分子电子学 光电开关 分子动力学 设计要素和原则 材料科学 离子运输机 离子通道
作者
Amit Ghosh,Jonathan R. Nitschke
出处
期刊:Accounts of Chemical Research [American Chemical Society]
卷期号:59 (2): 372-381 被引量:1
标识
DOI:10.1021/acs.accounts.5c00790
摘要

High Resolution Image Download MS PowerPoint Slide Conspectus Light offers a clean and precise means to control chemical processes. These advantages have opened the door to the development of dynamic host–guest systems, whose functions can be turned on or off with specific wavelengths. Over recent years, we have developed a suite of light-responsive metal–organic capsules that use azobenzene photoisomerization to direct functions that include reversible guest encapsulation, selective molecular separations, controlled catalysis, and directional mass transport. These capsules, assembled via subcomponent self-assembly, incorporate azobenzene-based ligands that undergo photoinduced trans – cis isomerization. This reversible switching induces cage disassembly or changes in host–guest binding, enabling light to act as an external signal to modulate activity. In this Account, we summarize five key studies that trace the evolution of this platform, from basic molecular recognition and guest release to complex, multicomponent systems capable of energy transduction and spatial molecular control. We describe (i) the design and mechanistic studies of phototriggered guest release using a tetrahedral Zn 4 L 4 cage; (ii) the use of an architecture built on this initial work to purify progesterone selectively from mixed steroidal systems; (iii) light-gated catalytic activation using a caged perrhenate system; (iv) selective lithium ion extraction using photoswitchable sandwich architecture; and (v) a Maxwell’s Demon-inspired setup that achieves directional molecular pumping across centimeter-scale distances. Collectively, these studies demonstrate how light-responsive metal–organic capsules can be programmed to perform diverse chemical functions, including guest release, selective separations, catalysis, ion extraction, and directional transport. This body of work establishes a platform for the future development of integrated, autonomous, and energy-efficient light-driven supramolecular technologies.
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