Protodefluorinated Selectfluor® heteroaggregate photoinduces direct C(sp3)–H fluorinations without photocatalyst†

Shahboz Yakubov , Joshua P. Barham
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引用次数: 0

Abstract

Herein, we uncover a hitherto hidden role of – a cheap, stable, recoverable by-product of radical C(sp3)–H fluorinations using Selectfluor®. This forms a photoactive, mixed heteroaggregate with Selectfluor® which underlies the reactivity of visible light photochemical fluorination reactions of unactivated C(sp3)–H bonds. Where previous reports claim to be ‘photocatalytic’, reactions work without photocatalyst when is dosed in at the start. Our results demonstrate that ‘photocatalysts’ are only necessary to generate a sufficient amount of nascent , whose heteroaggregate with Selectfluor® takes over as the main photoactive species. Mechanistic studies suggest the formation of a heteroaggregate between and Selectfluor® under photoirradiation, which generates . A salient feature of our H-TEDA(BF4)2-promoted method is its flexibility to use the C(sp3)–H precursor substrate as the limiting reactant, simplifying product isolations.
一种原去氟化selectflu®异质聚集体光诱导直接C(sp3)−H氟化无光催化剂
在这里,我们发现了H-TEDA(BF4)2的一个迄今为止隐藏的作用,这是一种廉价、稳定、可回收的自由基C(sp3) - h氟化的副产品。这与Selectfluor®形成了光活性的混合异质聚集体,这是可见光下未活化的C(sp3) -H键的光化学氟化反应的反应性基础。在以前的报道中声称是“光催化”的地方,当H-TEDA(BF4)2在开始时加入时,反应在没有光催化剂的情况下进行。我们的研究结果表明,“光催化剂”只需要产生足够数量的新生H-TEDA(BF4)2,其与Selectfluor®的异质聚集体成为主要的光活性物质。机理研究表明,在光照射下H-TEDA(BF4)2与Selectfluor®之间形成杂络合物,生成TEDA•2+。我们的方法的一个显著特点是它的灵活性,使用C(sp3) -H前驱体底物作为限制反应物,简化了从未反应的前驱体分离产物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.80
自引率
0.00%
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