化学
荧光
检出限
齿合度
锌
肉眼
环十二烷
核化学
水溶液
氨基三乙酸
无机化学
立体化学
结晶学
有机化学
螯合作用
晶体结构
色谱法
物理
量子力学
作者
Rui Wang,Shu‐Hui Yin,Bi‐Liu Lan,Heng‐Huan Ruan,Zhi‐Hui Qiu,Zhong Zhang
摘要
Two cyclen‐based multidentate N,O ligands, 1,4,7,10‐tetrazazcyclododecane‐N,N′,N″,N″′‐tetra‐ p ‐methylbenzoic acid (H 4 L 1 ) and 1,4,7,10‐tetrazazcyclododecane‐N,N′,N″,N″′‐tetra‐ p ‐cinnamic acid (H 4 L 2 ), were reacted with Zn (II) salts leading to a four‐fold interpenetrated 3D binodal PtS‐type network {[Zn 2 (HL 1 )Cl]·5H 2 O} n ( Zn‐1) along with a 1D ribbon‐like polymeric chain {[Zn 3 (HL 2 )Cl 3 (H 2 O) 2 ]·2CH 3 COCH 3 ·3H 2 O} n ( Zn‐2 ). Both two compounds exhibited excellent water stability in a wide pH range from 2 to 12 and emitted either UV or visible blue‐purple light. They can behave as recyclable fluorescent probes for highly selective sensing of nitrophenols with low detection limits. Additionally, the blue‐purple emission of Zn‐2 can be efficiently quenched by PA with a concentration as low as 20 μM; thus, the naked‐eye detection of PA can be fulfilled under a 365 nm UV lamp. Based on the DFT calculation and spectral analysis evidences, it can be proposed that the selective detection of nitrophenols by two Zn (II) compounds is owing to a synergistic effect of different quenching mechanisms along with the interactions between probes and analytes.
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