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方酸轮烷作为一种可逆光学氯离子传感器。

Squaraine rotaxane as a reversible optical chloride sensor.

机构信息

Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.

出版信息

Chemistry. 2010 Mar 1;16(9):2916-21. doi: 10.1002/chem.200902547.

Abstract

A mechanically interlocked squaraine rotaxane is comprised of a deep-red fluorescent squaraine dye inside a tetralactam macrocycle. NMR studies show that Cl(-) binding to the rotaxane induces macrocycle translocation away from the central squaraine station, a process that is completely reversed when the Cl(-) is removed from the solution. Steady-state fluorescence and excited-state lifetime measurements show that this reversible machine-like motion modulates several technically useful optical properties, including a three-fold increase in deep-red fluorescence emission that is observable to the naked eye. The excited states were characterized quantitatively by time-correlated single photon counting, femtosecond transient absorption spectroscopy, and nanosecond laser flash photolysis. Cl(-) binding to the rotaxane increases the squaraine excited singlet state lifetime from 1.5 to 3.1 ns, and decreases the excited triplet state lifetime from >200 to 44 micros. Apparently, the surrounding macrocycle quenches the excited singlet state of the encapsulated squaraine dye and stabilizes the excited triplet state. Prototype dipsticks were prepared by adsorbing the lipophilic rotaxane onto the ends of narrow, C18-coated, reverse-phase silica gel plates. The fluorescence intensity of a dipstick increased eighteen-fold upon dipping in an aqueous solution of tetrabutylammonium chloride (300 mM) and was subsequently reversed by washing with pure water. It is possible to develop the dipsticks for colorimetric determination of Cl(-) levels by the naked eye. After dipping into aqueous tetrabutylammonium chloride, a dipstick's color slowly fades at a rate that depends on the amount of Cl(-) in the aqueous solution. The fading process is due primarily to hydrolytic bleaching of the squaraine chromophore within the rotaxane. That is, association of Cl(-) to immobilized rotaxane induces macrocycle translocation and exposure of the electrophilic C(4)O(2) core of the squaraine station, which is in turn attacked by the ambient moisture to produce a bleached product.

摘要

一种机械互锁的方酸轮烷由一个深红色荧光方酸染料和一个四氢呋喃大环组成。NMR 研究表明,轮烷与 Cl(-)的结合诱导大环从中央方酸站迁移,当 Cl(-)从溶液中去除时,这个过程完全逆转。稳态荧光和激发态寿命测量表明,这种可逆的机器样运动调节了几个技术上有用的光学性质,包括肉眼可见的深红色荧光发射增加三倍。通过时间相关单光子计数、飞秒瞬态吸收光谱和纳秒激光闪光光解,对激发态进行了定量表征。Cl(-)与轮烷的结合将方酸激发单重态寿命从 1.5 ns 增加到 3.1 ns,并将激发三重态寿命从>200 ns 降低到 44 μs。显然,周围的大环猝灭了封装的方酸染料的激发单重态,并稳定了激发三重态。通过将亲脂性轮烷吸附在窄的、C18 涂覆的反相硅胶板的末端,制备了原型试条。将试条浸入 300 mM 的四丁基氯化铵水溶液中,荧光强度增加了 18 倍,然后用纯水冲洗即可逆转。通过肉眼可以开发用于比色测定 Cl(-)水平的试条。将试条浸入四丁基氯化铵水溶液后,其颜色会缓慢褪色,褪色速率取决于水溶液中 Cl(-)的含量。褪色过程主要归因于轮烷内方酸发色团的水解漂白。也就是说,Cl(-)与固定化轮烷的结合诱导大环迁移,并暴露出方酸站的亲电 C(4)O(2)核心,后者反过来被环境水分攻击,生成漂白产物。

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