磷光
系统间交叉
超分子化学
水溶液中的金属离子
吡啶
三吡啶
离子
主客化学
化学
水溶液
单重态
光化学
超分子组装
氢键
余辉
材料科学
金属
纳米技术
结晶学
荧光
物理化学
分子
晶体结构
有机化学
物理
原子物理学
伽马射线暴
天文
激发态
量子力学
作者
Ran Cen,Ming Liu,Chun Liu,Qin Hui Leng,Qian Ren,Zhu Tao,Xin Xiao
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2024-04-16
卷期号:6 (5): 1992-1998
被引量:3
标识
DOI:10.1021/acsmaterialslett.4c00434
摘要
A multifunctional supramolecular assembly, comprising nor-seco-cucurbit[10]uril (ns-Q[10]) and tripyridine-bridged 4-(4-bromophenyl)pyridine (BTPY), has been constructed. The host–guest interaction between BTPY and ns-Q[10] resulted in a decrease in the singlet–triplet splitting energy (ΔEST), thereby enhancing the intersystem crossing process. Furthermore, the multiple hydrogen bonding interactions between BTPY@ns-Q[10] assembly and poly(vinyl alcohol) (PVA), as well as its own host–guest interaction, inhibited the nonradiative transitions, resulting in long-lived room temperature phosphorescence (RTP) (τ = 261.3 ms). This RTP material provided a potential method for constructing RTP materials for information encryption and anticounterfeiting through a host–guest strategy. Moreover, the terpyridine component of BTPY, known for its strong metal coordination ability, enables the BTPY@ns-Q[10] assembly to rapidly detect Fe2+ and Fe3+ ions in aqueous solution.
科研通智能强力驱动
Strongly Powered by AbleSci AI