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多阶段质子化实现分子反转对称性的开-关-开控制:阐明振子拉波特规则。

On-off-on Control of Molecular Inversion Symmetry via Multi-stage Protonation: Elucidating Vibronic Laporte Rule.

机构信息

Laboratory of Chemical Physics, Keemilise ja Bioloogilise Füüsika Instituut, Akadeemia tee 23, 12618, Tallinn, Estonia.

Institute of Chemistry, Tartu Ülikool, 14a Ravila Str, 50411, Tartu, Estonia.

出版信息

Angew Chem Int Ed Engl. 2022 Dec 19;61(51):e202212581. doi: 10.1002/anie.202212581. Epub 2022 Nov 22.

Abstract

The Laporte rule dictates that one- and two-photon absorption spectra of inversion-symmetric molecules should display alternatively forbidden electronic transitions; however, for organic fluorophores, drawing clear distinction between the symmetric- and non-inversion symmetric two-photon spectra is often obscured due to prevalent vibronic interactions. We take advantage of consecutive single- and double-protonation to break and then reconstitute inversion symmetry in a nominally symmetric diketopyrrolopyrrole, causing large changes in two-photon absorption. By performing detailed one- and two-photon titration experiments, with supporting quantum-chemical model calculations, we explain how certain low-frequency vibrational modes may lead to apparent deviations from the strict Laporte rule. As a result, the system may be indeed considered as an on-off-on inversion symmetry switch, opening new avenues for two-photon sensing applications.

摘要

拉波特规则规定,在具有反演对称性的分子中,单光子和双光子吸收光谱应该显示交替禁戒的电子跃迁;然而,对于有机荧光团,由于普遍存在的振子相互作用,通常难以清晰地区分对称和非反演对称的双光子光谱。我们利用连续的单质子化和双质子化来打破并重建名义上对称的二酮吡咯并吡咯中的反演对称性,导致双光子吸收发生大的变化。通过进行详细的单光子和双光子滴定实验,并辅以量子化学模型计算,我们解释了某些低频振动模式如何导致明显偏离严格的拉波特规则。因此,该体系可以被认为是一个开-关-开的反演对称开关,为双光子传感应用开辟了新的途径。

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