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基于激发态分子内质子转移的氟离子比率荧光探针。

A ratiometric fluorescent probe for fluoride ion employing the excited-state intramolecular proton transfer.

机构信息

Department of Chemistry, Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, Institute of Analytical Science, Northwest University, Xi'an 710069, Shaanxi, China.

出版信息

Talanta. 2009 Nov 15;80(1):92-7. doi: 10.1016/j.talanta.2009.06.030. Epub 2009 Jun 18.

Abstract

A ratiometric fluorescent probe 1 for fluoride ion was developed based on modulation of the excited-state intramolecular proton transfer (ESIPT) process of 2-(2'-hydroxyphenyl)benzimidazole (HPBI) through the hydroxyl group protection/deprotection reaction. The probe 1 was readily prepared by the reaction of HPBI with tert-butyldimethylsilyl chloride (TBS-Cl) and shows only fluorescence emission maximum at 360 nm. Upon treatment with fluoride in aqueous DMF solution, the TBS protective group of probe 1 was removed readily and ESIPT of the probe was switched on, which resulted in a decrease of the emission band at 360 nm and an increase of a new fluorescence peak around 454 nm. The fluorescent intensity ratio at 454 and 360 nm (I(454)/I(360)) increases linearly with fluoride ion concentration in the range 0.3-8.0 micromol L(-1) and the detection limit is 0.19 micromol L(-1). The proposed probe shows excellent selectivity toward fluoride ion over other common anions. The method has been successfully applied to the fluoride determination in toothpaste and tap water samples.

摘要

一种基于 2-(2'-羟基苯基)苯并咪唑(HPBI)的激发态分子内质子转移(ESIPT)过程的调制,通过羟基保护/脱保护反应,开发出用于氟离子的比率荧光探针 1。探针 1 可通过 HPBI 与叔丁基二甲基氯硅烷(TBS-Cl)的反应轻松制备,仅在 360nm 处显示荧光发射最大值。在含有水的 DMF 溶液中用氟处理时,探针 1 的 TBS 保护基团很容易被去除,探针的 ESIPT 被打开,导致在 360nm 处的发射带降低,在大约 454nm 处出现新的荧光峰。在 0.3-8.0μmol L(-1)范围内,454nm 和 360nm 处的荧光强度比(I(454)/I(360))与氟离子浓度呈线性增加,检测限为 0.19μmol L(-1)。与其他常见阴离子相比,该探针对氟离子表现出优异的选择性。该方法已成功应用于牙膏和自来水中氟化物的测定。

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