Pushing Chemical Boundaries with N-Heterocyclic Olefins (NHOs): From Catalysis to Main Group Element Chemistry

N-Heterocyclic olefins (NHOs) have gone from the topic of a few scattered (but important) reports in the early 1990s to very recently being a ligand/reagent of choice in the far-reaching research fields of organocatalysis, olefin and heterocycle polymerization, and low oxidation state main group element chemistry. NHOs are formally derived by appending an alkylidene (CR₂) unit onto an N-heterocyclic carbene (NHC), and their pronounced ylidic character leads to high nucleophilicity and soft Lewis basic character at the ligating carbon atom. These olefinic donors can also be structurally derived from imidazole, triazole, and thiazole-based heterocyclic carbenes and, as a result, have highly tunable electronic and steric properties. In this Account, we will focus on various synthetic routes to imidazole-2-ylidene derived NHOs (sometimes referred to as deoxy-Breslow intermediates) followed by a discussion of the electron-donor ability of this structurally tunable ligand group. It should be mentioned that NHOs have a close structural analogy with Breslow-type intermediates, N-heterocyclic ketene aminals, and β-azolium ylides; while these latter species play important roles in advancing synthetic organic chemistry, discussion in this Account will be confined mostly to imidazole-2-ylidene derived NHOs. In addition, we will cover selected examples from the literature where NHOs and their anionic counterparts, N-heterocyclic vinylenes, are used to access reactive main group species not attainable using traditional ligands. Added motivation for these studies comes from the emerging number of low coordinate main group element based compounds that display reactivity once reserved for precious metal complexes (such as H-H and C-H bond activation). Moreover, NHOs are versatile precursors to new mixed element (P/C and N/C), and potentially bidentate, ligand constructs of great potential in catalysis, where various metal oxidation states and coordination environments need to be stabilized during a catalytic cycle. The most active area of recent growth for NHOs is their use as nucleophiles to promote efficient organocatalytic transformations, including transesterification, carbonyl reduction, and the conversion of CO₂ into value added products. Polyesters have also been generated through the NHO-promoted ring-opening polymerization of lactones, and the highly tunable nature of NHO organocatalysts allows for the rapid screening and enhancement of catalytic performance. Therefore, the growing utility of NHOs in the realm of organic and polymer chemistry can be viewed as evidence of the widespread impact of N-heterocyclic olefins on the chemical community. It is hoped that through this Account others will join this flourishing research domain and that the rapid recent growth of NHO chemistry is sustained for the foreseeable future.