电荷转移络合光化学中手性的诱导

IF 3.261
Tadashi Mori
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引用次数: 0

摘要

电子供体和受体在溶液中结合形成弱分子络合物,即电荷转移络合物。配合物的形成是明显的,其新的低能吸收带。在该电荷转移带的光激发下,配合物内的电子转移易于形成接触离子自由基对。复合体的形成和随后的光诱导电子转移过程的理论基础在半个世纪前就已经很好地建立了。然而,由于其自由基离子对的合成效用,电荷转移复合光化学现在正处于复兴之中。通过有意地避开非生产性的反向电子转移过程,在有或没有外部试剂和/或催化剂的情况下有效地获得所需的产品。此外,配合物的光激发不需要任何额外的光催化剂,通常可以想象与可见光。因此,在过去的二十年中,各种各样的供体/受体对和合成应用已经成为新的光反应体系。一些人还研究了立体选择性转化。本文综述了基于电荷转移络合物的光激发和光氧化还原催化的不对称光反应的最新进展,特别是在合成方面的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Induction of chirality in the charge transfer complex photochemistry

Electron donor and acceptor undergo association in solution to form a weak molecular complex, namely a charge transfer complex. The formation of the complex is apparent by its new low-energy absorption band. Upon photoexcitation of this charge transfer band, an intracomplex electron transfer is facilitated to form a contact ion radical pair. The theoretical basis for the complex formation and the subsequent photoinduced electron transfer process has been well established already half a century ago. Nevertheless, the charge transfer complex photochemistry is now in a renaissance, due to its synthetic utility of its radical ion pair. By intentionally sidestepped unproductive back electron transfer process, a desired product is effectively obtained with or without external reagent and/or catalyst. In addition, the photoexcitation of the complex does not require any additional photocatalyst and often conceivable with the visible light. Accordingly, various donor/acceptor pairs and synthetic applications have been emerged as novel photoreaction systems in the last two decades. Some have also addressed the stereoselective transformations. This mini review highlights the recent progress of the asymmetric photoreaction, in particular in synthetic applications, based on the photoexcitation of the charge transfer complex, in comparison with photoredox catalysis.

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CiteScore
4.10
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