光化学
光激发
光催化
超分子化学
罗丹明6G
电子转移
化学
费斯特共振能量转移
罗丹明B
材料科学
纳米技术
荧光
激发态
分子
有机化学
光学
催化作用
物理
核物理学
作者
Hechuan Li,Jianhua Yang,Danyang Li,Xuezhao Li,Jianxu Li,Cheng He
标识
DOI:10.1002/anie.202409094
摘要
Abstract Supramolecular artificial light‐harvesting system with highly efficient host–guest energy transfer pathway provides an ideal platform for optimizing the photochemistry process. The consecutive photo‐induced electron transfer (conPET) process overcomes the energy limitation of visible‐light photocatalysis, but is often compromised by mismatching between the absorption of ground state dye and its radical, weakening the efficiency of photoredox reaction. By encapsulating a conPET photocatalyst rhodamine 6G into metal‐organic cage, the supramolecular approach was undertaken to tackle the intrinsic difficulty of matching the light absorption of photoexcitation between rhodamine 6G and its radical. The highly efficient Förster resonance energy transfer from the photoexcited cage to rhodamine 6G forced by host–guest encapsulation facilitates the conPET process for the single‐wavelength light‐driven activation of aryl halides by stabilizing and accelerating the production and accumulation of the rhodamine 6G radical intermediate. The tunable and flexible nature of the supramolecular host–guest complex renders the cage‐based encapsulation strategy promising for the development of ideal photocatalysts toward the better utilization of solar energy.
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