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首页> 外文期刊>Beilstein journal of organic chemistry. >A new fluorescent chemosensor for fluoride anion based on a pyrrole–isoxazole derivative
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A new fluorescent chemosensor for fluoride anion based on a pyrrole–isoxazole derivative

机译:基于吡咯-异恶唑衍生物的新型氟离子荧光化学传感器

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Molecules containing polarized NH fragments that behave as anion-binding motifs are widely used as receptors for recognition and sensing purposes in aprotic solvents. We present here a new example of a receptor, 3-amino-5-(4,5,6,7-tetrahydro-1H-indol-2-yl)isoxazole-4-carboxamide (receptor 1), which contains pyrrole, amide and amino subunits. This receptor shows both changes in its UV–vis absorption and fluorescence emission spectra upon the addition of F?, resulting in highly selectivity for fluoride detection over other anions, such as Cl?, Br?, I?, HSO4?, H2PO4? and AcO? in CH3CN. 1H NMR titration, time-dependent density functional theory (TDDFT) calculations and other experiments confirm that the sensing process is brought about by deprotonation of the pyrrole-NH in receptor 1.
机译:含有充当阴离子结合基序的极化NH片段的分子被广泛用作非质子溶剂中识别和感测目的的受体。我们在这里提出了一个新的受体的例子,3-氨基-5-(4,5,6,7-四氢-1H-吲哚-2-基)异唑-4羧酰胺(受体1),其中含有吡咯,酰胺和氨基亚基。加入F 2时,该受体的紫外可见吸收光谱和荧光发射光谱均发生变化,从而对氟离子的检测具有很高的选择性,优于其他阴离子,例如Cl 2,Br 2,I 2,HSO 4 4,H 2 PO 4 2。和AcO?在CH3CN中。 1 H NMR滴定,随时间变化的密度泛函理论(TDDFT)计算和其他实验证实,传感过程是由受体1中吡咯-NH的去质子化引起的。

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