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Supported Lanthanum Borohydride Catalyzes CH Borylation Inside Zeolite Micropores.

Yuting LiUddhav KanburJinlei CuiGuocang WangTakeshi KobayashiAaron D SadowLong Qi
Published in: Angewandte Chemie (International ed. in English) (2022)
The zeolite-supported lanthanide La(BH 4 ) x -HY 30 catalyzes C-H borylation of benzene with pinacolborane (HBpin), providing a complementary approach to precious, late transition metal-catalyzed borylations. The reactive catalytic species are generated from La grafted at the Brønsted acid sites (BAS) in micropores of the zeolite, whereas silanoate- and aluminoate-grafted sites are inactive under the reaction conditions. During typical catalytic borylations, conversion to phenyl pinacolborane (PhBpin) is zero-order in HBpin concentration. A turnover number (TON) of 167 is accessed by capping external silanols, selectively grafting at BAS sites, and adding HBpin slowly to the reaction.
Keyphrases
  • transition metal
  • room temperature
  • crystal structure
  • single molecule
  • electron transfer
  • metal organic framework