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与圆偏振光子的强耦合:迈向腔诱导的对映选择性。

Strong Coupling to Circularly Polarized Photons: Toward Cavity-Induced Enantioselectivity.

作者信息

Riso Rosario R, Ronca Enrico, Koch Henrik

机构信息

Department of Chemistry, Norwegian University of Science and Technology, 7491 Trondheim, Norway.

Department of Chemistry, Biology and Biotechnology, University of Perugia, Via Elce di Sotto 8, 06123 Perugia, Italy.

出版信息

J Phys Chem Lett. 2024 Aug 29;15(34):8838-8844. doi: 10.1021/acs.jpclett.4c01701. Epub 2024 Aug 21.

Abstract

The development of new methodologies for the selective synthesis of individual enantiomers is still one of the major challenges in synthetic chemistry. Many biomolecules, and also many pharmaceutical compounds, are indeed chiral. While the use of chiral reactants or catalysts has led to substantial progress in the field of asymmetric synthesis, a systematic approach applicable to general reactions has still not been proposed. In this work, we demonstrate that strong coupling to circularly polarized fields can induce asymmetry in otherwise nonselective reactions. Specifically, we show that the field induces stereoselectivity in the early stages of chemical reactions by selecting an energetically preferred direction of approach for the reagents. Although the effects observed thus far are too small to significantly drive asymmetric synthesis, our results provide a proof of principle for field-induced stereoselective mechanisms. These findings lay the groundwork for future research.

摘要

开发用于选择性合成单个对映体的新方法仍然是合成化学中的主要挑战之一。许多生物分子以及许多药物化合物确实是手性的。虽然使用手性反应物或催化剂在不对称合成领域取得了重大进展,但尚未提出适用于一般反应的系统方法。在这项工作中,我们证明与圆偏振场的强耦合可以在其他非选择性反应中诱导不对称性。具体而言,我们表明该场通过为试剂选择能量上更优选的接近方向,在化学反应的早期阶段诱导立体选择性。尽管到目前为止观察到的效应太小,无法显著推动不对称合成,但我们的结果为场诱导的立体选择性机制提供了原理证明。这些发现为未来的研究奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc0e/11372830/6ebe07f7f972/jz4c01701_0001.jpg

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