化学
磷光
胺气处理
锌
无机化学
有机化学
荧光
量子力学
物理
作者
Lei Miao,Bolun Zhang,Weimin Song,Jun Chen,Wen-Jing Shi,Rui-Hong Wang,Shu‐Qin Liu,Ying-Jia Li,Jianjun Zhang
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2025-04-02
卷期号:64 (14): 7214-7223
被引量:2
标识
DOI:10.1021/acs.inorgchem.5c00917
摘要
Molecular-based afterglow materials have garnered significant attention due to their diverse applications. However, most studies focus on conventional luminophores, leaving nonconventional systems underexplored, particularly regarding the screening of new material subclasses and the development of applications such as sensing. Herein we report the successful preparation of two new two-dimensional ZnSO4-based open-framework materials (OFMs)─(H2DABCO)[Zn3(μ3-OH)2(SO4)3]·H2O (1) and (H2DABCO)[Zn(SO4)2] (2)─through self-assembly of Zn2+/SO42– with nonaromatic triethylenediamine (DABCO). Both compounds exhibit distinct delayed emission characteristics with lifetimes of 259.10 ms (1) and 49.62 μs (2), respectively. Frontier orbital analysis reveals the key role of charge transfer between sulfate groups to (H2DABCO)2+ cations in the luminescence. Notably, 1 demonstrates exceptional performance as an afterglow probe for the selective detection of n-propylamine and n-butylamine vapors, achieving detection limits of 32.99 and 47.18 ppm, respectively. The sensing mechanism involves a phase-transition process, and the luminescence change can be observed by the naked eye. This work pioneers the integration of sulfate-based OFMs with nonconventional room-temperature phosphorescence properties, demonstrating their potential as afterglow probes for industrial and environmental monitoring.
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