脱质子化
化学
滴定法
荧光
水溶液
离子
化学计量学
分析化学(期刊)
结合常数
水溶液中的金属离子
检出限
质子核磁共振
配合物的稳定常数
无机化学
物理化学
立体化学
有机化学
结合位点
色谱法
生物化学
物理
量子力学
作者
Muthaiah Shellaiah,Yen-Hsing Wu,Hong‐Cheu Lin
出处
期刊:Analyst
[Royal Society of Chemistry]
日期:2013-01-01
卷期号:138 (10): 2931-2931
被引量:126
摘要
Simple pyridyl-salicylimine derivatives (F1, F2 and F3) are reported for the first time as fluorescence "turn-on" sensors for distinct detections of Zn2+, Al3+ and OH− ions in mixed-aqueous media CH3CN/H2O with volume ratios of 6/4 and 3/7 (at pH = 7 and 25 °C) via internal charge transfer (ICT), chelation enhanced fluorescence (CHEF), and deprotonation mechanisms. F1 and F2 show diverse turn-on sensing applications to Zn2+, Al3+ and OH− ions, but F3 exhibited the fluorescence turn-on sensing to Al3+ and OH− ions in CH3CN/H2O (6/4; vol/vol). F1+Zn2+ and F2+Zn2+ complexes revealed the reversibilities and ratiometric displacements of Zn2+ with ethylene diamine tetra acetic acid (EDTA) and Al3+ ions, respectively, in CH3CN/H2O (6/4; vol/vol). On the other hand, F1, F2 and F3 in CH3CN/H2O (3/7; vol/vol) showed sensitivities only to Al3+ ions but negligible selectivities to OH− ions. Stoichiometry of all sensor complexes were calculated as 1 : 1 by job's plots based on UV/Vis and PL titrations. The complex formation and binding sites of all sensor materials were well characterized by 1H, 13C NMR, and mass (FAB) spectral analysis. Detection limits were calculated from standard deviations and linear fitting calculations. The association constant (log Ka) values of sensor complexes were evaluated from the fluorescence binding isotherms. The fluorescence decay constant (τ) values were estimated from time resolved fluorescence studies. Time, temperature, pH and solvent concentration effects towards sensor responses were fully investigated in this report.
科研通智能强力驱动
Strongly Powered by AbleSci AI