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细菌光捕获复合物中类胡萝卜素单线态裂变反应的三重态激发谱揭示。

Carotenoid Singlet Fission Reactions in Bacterial Light Harvesting Complexes As Revealed by Triplet Excitation Profiles.

机构信息

Department of Chemistry, Renmin University of China , Beijing 100872, P. R. China.

Faculty of Science, Ibaraki University , Mito 310-8512, Japan.

出版信息

J Am Chem Soc. 2017 Nov 8;139(44):15984-15993. doi: 10.1021/jacs.7b09809. Epub 2017 Oct 26.

Abstract

Carotenoids (Cars) in bacterial photosynthesis are known as accessory light harvesters and photoprotectors. Recently, the singlet fission (SF) reaction initiated by Car photoabsorption has been recognized to be an effective excitation deactivation channel disfavoring the light harvesting function. Since the SF reaction and the triplet sensitization reaction underlying photoprotection both yield triplet excited state Cars (Car*), their contribution to the overall Car* photoproduction are difficult to disentangle. To tackle this problem, we resorted to the triplet excitation profiles (TEPs), i.e., the actinic spectra of the overall Car* photoproduction. The TEPs combined with the conventional fluorescence excitation spectra allowed us to extract the neat SF contribution, which can serve as a spectroscopic measure for the SF reactivity. This novel spectroscopic strategy was applied to analyze the light harvesting complexes (LHs) from Tch. tepidum and Rba. sphaeroides 2.4.1. The results unambiguously showed that the SF reaction of Cars proceeds with an intramolecular scheme, even in the case of LH1-RC from Rba. sphaeroides 2.4.1 likely binding a secondary pool of Cars. Regarding the SF-reactivity, the geometric distortion in the conjugated backbone of Cars was shown to be the structural determinant, while the length of the Car conjugation was suggested to be relevant to the effective localization of the geminate triplets to avoid being annihilated. The SF reaction scheme and structure-activity relationship revealed herein will be useful not only in deepening our understanding of the roles of Cars in photosynthesis, but also in enlightening the applications of Cars in artificial light conversion systems.

摘要

类胡萝卜素(Cars)在细菌光合作用中被称为辅助光捕获和光保护剂。最近,人们认识到 Car 光吸收引发的单重态裂变(SF)反应是一种有效的激发失活通道,不利于光捕获功能。由于 SF 反应和光保护所基于的三重态敏化反应都产生三重态激发态 Cars(Car*),因此很难区分它们对整体 Car光产生的贡献。为了解决这个问题,我们求助于三重态激发轮廓(TEP),即整体 Car光产生的光激发光谱。TEP 结合常规荧光激发光谱使我们能够提取出纯净的 SF 贡献,这可以作为 SF 反应性的光谱测量。这种新的光谱策略被应用于分析来自 Tch. tepidum 和 Rba. sphaeroides 2.4.1 的光捕获复合物(LH)。结果明确表明,即使在 Rba. sphaeroides 2.4.1 的 LH1-RC 可能结合了 Cars 的第二个池的情况下,Cars 的 SF 反应也以分子内方案进行。关于 SF 反应性,Car 共轭主链中的几何变形被证明是结构决定因素,而 Car 共轭的长度被认为与有效地将孪生三重态定位以避免被消除有关。本文揭示的 SF 反应方案和结构-活性关系不仅有助于加深我们对 Cars 在光合作用中的作用的理解,而且有助于启发 Cars 在人工光转换系统中的应用。

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