Iron-borane catalyzed carbonyl hydroboration and isolation of an iron(I)-ketyl radical

Abstract

Abstract Hydroboration of carbonyl compounds has proven a pivotal route to access alcohols and other C1 moieties in recent years. Despite this, iron-based catalyst systems are somewhat limited with very little mechanistic understanding of these systems developed. Here we show that an iron metalloborane complex [{( i Pr DPB Ph )Fe} 2 (μ−1,2-N 2 )] ( A ) is an efficient pre-catalyst for hydroboration of ketones, cyclic esters and CO 2 with mild conditions. Mechanistic insights reveal a previously unreported direct iron(0)-mediated ligand-to-ligand hydride transfer (LLHT) process is in operation with B–H bond breaking being rate determining, indicating the importance of mechanistic studies on well-known transformations. An iron(I)-benzophenone ketyl radical with a unique S  = 1 antiferromagnetic ground state has been isolated and fully characterized.