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高灵敏度和选择性的基于罗丹明的“关-开”可逆化学传感器用于锡(Sn4+)检测和活细胞成像。

Highly sensitive and selective rhodamine-based "off-on" reversible chemosensor for tin (Sn4+) and imaging in living cells.

机构信息

Department of Chemistry and ‡Centre for Healthcare Science & Technology, Bengal Engineering and Science University , Shibpur, Howrah-711103, India.

出版信息

Inorg Chem. 2013 Oct 7;52(19):10825-34. doi: 10.1021/ic4007026. Epub 2013 Sep 25.

Abstract

A structurally characterized new oxo-chromene functionalized rhodamine derivative L1 exhibits high selectivity toward Sn(4+) by forming a 1:1 complex, among other biologically important metal ions, as studied by fluorescence, absorption, and HRMS spectroscopy. Complexing with Sn(4+) triggers the formation of a highly fluorescent ring-open form which is pink in color. The sensor shows extremely high fluorescence enhancement upon complexation with Sn(4+), and it can be used as a "naked-eye" sensor. DFT computational studies carried out in mimicking the formation of a 1:1 complex between L1 and Sn(4+) resulted in a nearly planar pentacoordinate Sn(IV) complex. Studies reveal that the in situ prepared L1-Sn complex is selectively and fully reversible in presence of sulfide anions. Further, confocal microscopic studies confirmed that the receptor shows in vitro detection of Sn(4+) ions in RAW cells.

摘要

一种结构特征明确的新型氧杂色烯功能化罗丹明衍生物 L1 对 Sn(4+) 具有高度选择性,通过荧光、吸收和高分辨率质谱(HRMS)光谱研究,可与其他重要的生物金属离子形成 1:1 的配合物。与 Sn(4+) 配合会引发形成高度荧光开环形式,呈粉红色。该传感器与 Sn(4+) 配位后表现出极高的荧光增强,可以用作“肉眼”传感器。在模拟 L1 和 Sn(4+) 之间形成 1:1 配合物的情况下进行的 DFT 计算研究导致形成了近乎平面的五配位 Sn(IV)配合物。研究表明,在硫离子存在下,原位制备的 L1-Sn 配合物是选择性和完全可逆的。此外,共聚焦显微镜研究证实,该受体在 RAW 细胞中可体外检测 Sn(4+)离子。

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