Xing Chang, Qi Zhenhong, Zhou Bo, Yan Dongpeng, Fang Wei-Hai
Key Laboratory of Theoretical and Computational Photochemistry, Ministry of Education, College of Chemistry, Beijing Normal University, Beijing, 100875, P. R. China.
Angew Chem Int Ed Engl. 2024 May 21;63(21):e202402634. doi: 10.1002/anie.202402634. Epub 2024 Apr 3.
Molecular ultralong room-temperature phosphorescence (RTP), exhibiting multiple stimuli-responsive characteristics, has garnered considerable attention due to its potential applications in light-emitting devices, sensors, and information safety. This work proposes the utilization of photochemical cascade processes (PCCPs) in molecular crystals to design a stepwise smart RTP switch. By harnessing the sequential dynamics of photo-burst movement (induced by [2+2] photocycloaddition) and photochromism (induced by photogenerated radicals) in a bismuth (Bi)-based metal-organic halide (MOH), a continuous and photo-responsive ultralong RTP can be achieved. Furthermore, utilizing the same Bi-based MOH, diverse application demonstrations, such as multi-mode anti-counterfeiting and information encryption, can be easily implemented. This work thus not only serves as a proof-of-concept for the development of solid-state PCCPs that integrate photosalient effect and photochromism with light-chemical-mechanical energy conversion, but also lays the groundwork for designing new Bi-based MOHs with dynamically responsive ultralong RTP.
分子超长室温磷光(RTP)具有多种刺激响应特性,因其在发光器件、传感器和信息安全等方面的潜在应用而备受关注。这项工作提出利用分子晶体中的光化学级联过程(PCCP)来设计一种逐步智能RTP开关。通过利用铋(Bi)基金属有机卤化物(MOH)中光猝发运动(由[2+2]光环加成诱导)和光致变色(由光生自由基诱导)的顺序动力学,可以实现连续且光响应的超长RTP。此外,利用相同的铋基金属有机卤化物,可以轻松实现多种应用演示,如多模式防伪和信息加密。因此,这项工作不仅为将光突出效应和光致变色与光化学机械能转换相结合的固态PCCP的开发提供了概念验证,也为设计具有动态响应超长RTP的新型铋基金属有机卤化物奠定了基础。