Off–On Photo- and Redox-Triggered Anion Transport Using an Indole-Based Hydrogen Bond Switch

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-31 DOI:10.1021/acsomega.4c0788010.1021/acsomega.4c07880
Manzoor Ahmad, Andrew Muir and Matthew J. Langton*, 
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Abstract

A stimulus-responsive indole-based hydrogen bonding switch is reported, which enables off–on activation of transmembrane ion transport in response to photo- and redox triggers. This is achieved by alkylation of an indole-based anionophore, preorganized through intramolecular hydrogen bonding, with o-nitrobenzyl and azobenzene cages. This renders the anionophore inactive through formation of a six-membered intramolecular hydrogen bonding interaction and locking of the anion binding protons. Decaging with biologically relevant light and redox stimuli leads to efficient activation of anion transport across lipid bilayer membranes by unlocking the hydrogen bond donors, such that they are now available for anion binding and transport.

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利用吲哚基氢键开关实现光电和氧化还原触发的阴离子迁移
报告中介绍了一种刺激响应型吲哚基氢键开关,它能在光和氧化还原触发器的作用下,实现跨膜离子转运的开关激活。这是通过邻硝基苄基和偶氮苯笼子对通过分子内氢键预组织的吲哚基阴离子团进行烷基化而实现的。通过形成六元分子内氢键相互作用和锁定阴离子结合质子,使阴离子团失去活性。在与生物相关的光和氧化还原刺激下进行解分级,可通过解除氢键供体的锁定,有效激活阴离子在脂质双分子层膜上的转运,从而使其可用于阴离子的结合和转运。
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CiteScore
7.20
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4.30%
发文量
567
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