Regioselective Arene C–H Borylation with a MOF-Immobilized Iridium Bipyridine Catalyst
Abstract
High Resolution Image Download MS PowerPoint Slide Postsynthetic ligand exchange and metalation have been used to immobilize iridium bipyridine precatalysts in MFU-4 l with controlled loadings. The resulting materials, 1-Ir- x ( x = 0.1–0.5), exhibit high activity for catalytic C–H borylation of arenes, and 1-Ir-0.5 achieves up to 1560 turnover numbers per Ir for toluene substrate. Remarkably, 1-Ir-0.5 exhibits high meta: para product regioselectivity compared to a homogeneous catalyst analogue for arene substrates bearing bulky triisopropylsilyl groups. Density functional theory (DFT) calculations reveal that steric constraints imposed by metal-organic framework (MOF) pore confinement increase the free energy barrier for para C–H activation, biasing product formation toward the meta isomer.
Fields of Study & Subjects
Catalytic C–H Functionalization Methods
Organoboron and organosilicon chemistry
Catalytic Cross-Coupling Reactions
Publication details
- Journal / source
- ACS Applied Materials & Interfaces
- Publisher
- American Chemical Society (ACS)
- Volume
- 18
- Issue
- 7
- Pages
- 11467–11476
- Publication date
- 13 February 2026
- Language
- EN