Year: 2026
Type: article
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.
Institution: The Ohio State University
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
OpenAlex ID: W7128769043
