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Trifluoromethylative Bifunctionalization of Alkenes via a Bibenzothiazole-Derived Photocatalyst under Both Visible- and Near-Infrared-Light Irradiation
ACS Catalysis ( IF 12.9 ) Pub Date : 2023-06-02 , DOI: 10.1021/acscatal.3c01812
Bidyut Kumar Kundu 1 , Chuang Han 1 , Prasenjit Srivastava 2 , Siddhant Nagar 1 , Katie E. White 2 , Jeanette A. Krause 1 , Christopher G. Elles 2 , Yujie Sun 1
Affiliation  

The incorporation of trifluoromethyl groups into organic molecules such as agrochemicals and pharmaceuticals has attracted a significant amount of interest because they will impact the binding ability, lipophilicity, metabolic stability, and chemical stability of the resulting molecules. Over the past few years, photocatalytic trifluoromethylation of aryl alkenes has been reported, which typically requires precious Ru/Ir-containing photocatalytic systems. Herein, we report a metal-free organic photocatalyst composed of a bibenzothiazole core and two imine-bridged methoxyphenyl substituents (dBIP–OMe), which is able to drive trifluoromethylative bifunctionalization of alkenes photocatalytically without the use of any sacrificial reagents. Mechanistic studies reveal two consecutive single-electron-transfer steps between the excited dBIP–OMe*, the CF3 precursor (Umemoto’s reagent), and the alkene substrate. Substrate scope studies demonstrated that our trifluoromethylative bifunctionalization strategy using dBIP–OMe is applicable for both aryl and aliphatic alkenes. Furthermore, a variety of nucleophiles, such as H2O, acetate, cyanide, azide, etc., can be readily incorporated into the carbocation intermediate once the foremost trifluoromethylation step is accomplished, substantially broadening the application scope of this photocatalytic method. Finally, taking advantage of the two-photon absorption capability of dBIP–OMe in the near-infrared region, we demonstrated that the hydroxytrifluoromethylation of styrene could be achieved using an inexpensive 740 nm LED as the sole light source.

中文翻译:

在可见光和近红外光照射下通过联苯并噻唑衍生的光催化剂实现烯烃的三氟甲基化双功能化

将三氟甲基结合到有机分子(如农用化学品和药物)中引起了极大的兴趣,因为它们会影响所得分子的结合能力、亲脂性、代谢稳定性和化学稳定性。在过去几年中,报道了芳基烯烃的光催化三氟甲基化,这通常需要珍贵的含 Ru/Ir 的光催化系统。在此,我们报道了一种由联苯并噻唑核和两个亚胺桥联的甲氧基苯基取代基(dBIP-OMe)组成的无金属有机光催化剂),它能够在不使用任何牺牲试剂的情况下光催化驱动烯烃的三氟甲基化双功能化。机理研究揭示了激发的dBIP–OMe *、CF 3前体(Umemoto 试剂)和烯烃底物之间的两个连续的单电子转移步骤。底物范围研究表明,我们使用dBIP-OMe 的三氟甲基化双功能化策略适用于芳基和脂肪族烯烃。此外,各种亲核试剂,如 H 2一旦最重要的三氟甲基化步骤完成,O、乙酸盐、氰化物、叠氮化物等就可以很容易地结合到碳阳离子中间体中,大大拓宽了这种光催化方法的应用范围。最后,利用dBIP-OMe在近红外区域的双光子吸收能力,我们证明了使用廉价的 740 nm LED 作为唯一光源可以实现苯乙烯的羟基三氟甲基化。
更新日期:2023-06-02
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