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仿生系统触发基于苯并噻唑的分子开关“开启”荧光。

Biomimetic systems trigger a benzothiazole based molecular switch to 'turn on' fluorescence.

机构信息

Department of Chemistry, Visvesvaraya National Institute of Technology, Nagpur, Maharashtra 440010, India; Institute of Chemical Technology Mumbai-Marathwada Campus, Jalna, Maharashtra 431203, India.

Department of Chemistry, Visvesvaraya National Institute of Technology, Nagpur, Maharashtra 440010, India.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2019 Jun 15;217:197-205. doi: 10.1016/j.saa.2019.03.089. Epub 2019 Mar 26.

Abstract

Molecular switches are valuable tools for the detection of many chemical and biological processes. On the other hand, Schiff bases are known for their simplicity in synthesis and their enormous biochemical applications. In this scenario, when a strategically designed Schiff base acts as a molecular switch in biomimetic environments drags inevitable attention. In this article, we hereby demonstrate an interesting behavior of a strategically designed bioactive benzothiazole based Schiff base (E)-2-(((6-chlorobenzo[d]thiazol-2-ylimino)methyl)-5-diethylamino) phenol (CBMDP) whose fluorescence characteristics dramatically modulate as consequence of its structural modification in aqueous and biomimetic environments individually. Electronic absorption, steady state and time resolved fluorescence spectroscopic techniques along with DFT based quantum chemical calculation evidence that in pure organic solvents CBMDP exists in highly fluorescent enol-imine (N) form which transform into feebly fluorescent hydrated species (H) in bulk aqueous media. Contrariwise, on interaction with the ionic and non-ionic micellar media or with liposome, a structural restoration occurs from less fluorescent hydrated (H) species into a highly fluorescent normal (N) one. This molecular flipping of the title compound upon micellar compartmentalization is possibly caused by the micropolarity of the local environment and further supported by its spectral behavior in different polarity gradient solvent mixture of water-dioxane (protic-aprotic) and water-methanol (protic -protic). Usually, Schiff bases are prone to hydrolysis in aqueous media, interestingly, the structural framework of this strategically designed molecule only allow the first step of hydrolysis, which is hydration of azomethine linkage whereas it withstand the second step, and that possibly helps the structural restoration process. Hence the article described herein may emphasize how a systematically designed Schiff base framework can be used as 'turn off- turn on' fluorescent molecular switch which may be extremely useful for its applications in the area of biochemical sensors.

摘要

分子开关是检测许多化学和生物过程的有价值的工具。另一方面,席夫碱因其合成简单且具有巨大的生化应用而闻名。在这种情况下,当一个经过策略设计的席夫碱在仿生环境中充当分子开关时,会引起人们的关注。在本文中,我们展示了一种经过策略设计的生物活性苯并噻唑基席夫碱(E)-2-((6-氯苯并[d]噻唑-2-基亚氨基)甲基)-5-二乙氨基)苯酚(CBMDP)的有趣行为,其荧光特性因其在水相和仿生环境中的结构修饰而发生显著调制。电子吸收、稳态和时间分辨荧光光谱技术以及基于 DFT 的量子化学计算证明,在纯有机溶剂中,CBMDP 以高度荧光的烯醇-亚胺(N)形式存在,在大量水介质中转化为弱荧光的水合物种(H)。相反,与离子和非离子胶束介质或脂质体相互作用时,结构从较弱荧光的水合(H)物种恢复为高度荧光的正常(N)物种。标题化合物在胶束分隔化时的这种分子翻转可能是由局部环境的微极性引起的,并且进一步得到了其在不同极性梯度溶剂混合物(水-二氧六环(质子-非质子)和水-甲醇(质子-质子))中的光谱行为的支持。通常,席夫碱在水介质中容易水解,有趣的是,这个经过策略设计的分子的结构框架只允许水解的第一步,即亚胺键的水合,而它能抵抗第二步,这可能有助于结构恢复过程。因此,本文描述的内容强调了如何将一个经过系统设计的席夫碱框架用作“关-开”荧光分子开关,这对于其在生化传感器领域的应用可能非常有用。

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