Talavera Maria, von Hahmann Cortney N, Müller Robert, Ahrens Mike, Kaupp Martin, Braun Thomas
Department of Chemistry, Humboldt Universität zu Berlin, Brook-Taylor-Strasse 2, 12489, Berlin, Germany.
Institut für Chemie, Theoretische Chemie/Quantenchemie, Sekr. C7, Technische Universität Berlin, Strasse des 17. Juni 135, 10623, Berlin, Germany.
Angew Chem Int Ed Engl. 2019 Jul 29;58(31):10688-10692. doi: 10.1002/anie.201902872. Epub 2019 Jul 1.
The reaction of [Rh(H)(PEt ) ] (1) with the refrigerant HFO-1234yf (2,3,3,3-tetrafluoropropene) affords an efficient route to obtain [Rh(F)(PEt ) ] (3) by C-F bond activation. Catalytic hydrodefluorinations were achieved in the presence of the silane HSiPh . In the presence of a fluorosilane, 3 provides a C-H bond activation followed by a 1,2-fluorine shift to produce [Rh{(E)-C(CF )=CHF}(PEt ) ] (4). Similar rearrangements of HFO-1234yf were observed at [Rh(E)(PEt ) ] [E=Bpin (6), C D (8), Me (9)]. The ability to favor C-H bond activation using 3 and fluorosilane is also demonstrated with 3,3,3-trifluoropropene. Studies are supported by DFT calculations.
[Rh(H)(PEt₃)₃] (1) 与制冷剂HFO - 1234yf(2,3,3,3 - 四氟丙烯)反应,通过C - F键活化提供了一条获得[Rh(F)(PEt₃)₃] (3) 的有效途径。在硅烷HSiPh₃存在下实现了催化加氢脱氟反应。在氟硅烷存在下,3会引发C - H键活化,随后发生1,2 - 氟迁移,生成[Rh{(E)-C(CF₃)=CHF}(PEt₃)₃] (4)。在[Rh(E)(PEt₃)₃] [E = Bpin (6)、C₆D₆ (8)、Me (9)] 中也观察到了HFO - 1234yf的类似重排。使用3和氟硅烷促进C - H键活化的能力在3,3,3 - 三氟丙烯中也得到了证明。研究得到了密度泛函理论计算的支持。