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When SF5outplays CF3: effects of pentafluorosulfanyl decorated scorpionates on copper
Fecha de emisión
2021-11-21
Autor(es)
Noonikara-Poyil, Anurag
Muñoz-Castro, Álvaro
Boretskyi, Andrii
Mykhailiuk, Pavel K.
Dias, H. V. Rasika
DOI
10.1039/d1sc04846e
Resumen
Polyfluorinated, electron-withdrawing, and sterically demanding supporting ligands are of significant value in chemistry. Here we report the assembly and use of a bis(pyrazolyl)borate, [Ph2B(3-(SF5)Pz)2]−that combines all such features, and involves underutilized pentafluorosulfanyl substituents. The ethylene and carbonyl chemistry of copper(i) supported by [Ph2B(3-(SF5)Pz)2]−, a comparison to the trifluoromethylated counterparts involving [Ph2B(3-(CF3)Pz)2]−, as well as copper catalyzed cyclopropanation of styrene with ethyl diazoacetate and CF3CHN2are presented. The results from cyclopropanation show that SF5groups dramatically improved the yields and stereoselectivity compared to the CF3 © The Royal Society of Chemistry 2021.
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