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氧化还原活性大环的多模态切换。

Multimodal switching of a redox-active macrocycle.

机构信息

WPI Center for Materials Nanoarchitectonics, National Institute for Materials Science, Namiki 1-1, Tsukuba, Ibaraki, 305-0044, Japan.

School of Chemistry, University of Birmingham, Edgbaston, Birmingham, West Midlands, B15 2TT, UK.

出版信息

Nat Commun. 2019 Mar 1;10(1):1007. doi: 10.1038/s41467-019-08978-5.

Abstract

Molecules that can exist in multiple states with the possibility of toggling between those states based on different stimuli have potential for use in molecular switching or sensing applications. Multimodal chemical or photochemical oxidative switching of an antioxidant-substituted resorcinarene macrocycle is reported. Intramolecular charge-transfer states, involving hemiquinhydrones are probed and these interactions are used to construct an oxidation-state-coupled molecular switching manifold that reports its switch-state conformation via striking variation in its electronic absorption spectra. The coupling of two different oxidation states with two different charge-transfer states within one macrocyclic scaffold delivers up to five different optical outputs. This molecular switching manifold exploits intramolecular coupling of multiple redox active substituents within a single molecule.

摘要

报道了一种抗氧化剂取代的杯[4]芳烃大环的多模式化学或光化学氧化切换。探测了涉及半醌氢醌的分子内电荷转移态,并利用这些相互作用构建了一个氧化态耦合的分子开关流形,通过其电子吸收光谱的显著变化来报告其开关态构象。在一个大环支架内将两个不同的氧化态与两个不同的电荷转移态耦合,可提供多达五个不同的光学输出。这个分子开关流形利用了单个分子内多个氧化还原活性取代基的分子内耦合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/421f/6397175/319715fc744b/41467_2019_8978_Fig1_HTML.jpg

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