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电化学交叉偶联在广泛电流密度范围内具有意外的高稳健性。

Unexpected high robustness of electrochemical cross-coupling for a broad range of current density.

作者信息

Wiebe Anton, Riehl Barbara, Lips Sebastian, Franke Robert, Waldvogel Siegfried R

机构信息

Institut für Organische Chemie, Johannes Gutenberg-Universität Mainz, Duesbergweg 10-14, 55128 Mainz, Germany.

Max Planck Graduate Center, Staudingerweg 9, 55128 Mainz, Germany.

出版信息

Sci Adv. 2017 Oct 6;3(10):eaao3920. doi: 10.1126/sciadv.aao3920. eCollection 2017 Oct.

Abstract

Electro-organic synthesis is a powerful technique for the sustainable preparation of compounds. However, many electrosynthetic reactions require complex equipment, are limited to a very narrow current density range, or have very long reaction times; some also involve nonselective transformations and bad scalability. The robust and selective synthesis of nonsymmetric biphenols and partially protected derivatives is established by anodic C-C cross-coupling. The setup is simple, involving constant current conditions and undivided cells. Its key is a unique electrolyte system based on fluorous alcohols and mixtures, particularly 1,1,1,3,3,3-hexafluoroisopropanol. This allows variations of the current density of more than two orders of magnitude without decreasing selectivity or product yield. This exceptional effect is unknown for electro-organic synthesis of products that have similar oxidation potentials as the starting materials. It potentially paves the way for industrial electrolyzers with variable current consumption, which could enable the flexible use of energy surplus in the electricity supply.

摘要

有机电合成是一种用于可持续制备化合物的强大技术。然而,许多电合成反应需要复杂的设备,限于非常窄的电流密度范围,或具有很长的反应时间;有些还涉及非选择性转化和较差的可扩展性。通过阳极C-C交叉偶联实现了非对称联苯酚及其部分保护衍生物的稳健且选择性合成。该装置简单,涉及恒流条件和无隔膜电解槽。其关键是基于氟代醇及其混合物,特别是1,1,1,3,3,3-六氟异丙醇的独特电解质体系。这使得电流密度变化超过两个数量级而不降低选择性或产物收率。对于与起始原料具有相似氧化电位的产物的有机电合成而言,这种特殊效果是未知的。它可能为可变电流消耗的工业电解槽铺平道路,这能够灵活利用电力供应中的过剩能源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b449/5630235/9bdce2660bb7/aao3920-F1.jpg

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