Three-Coordinate Formal Cobalt(0), Iron(0), and Manganese(0) Complexes with Persistent Carbene and Alkene Ligation.

Low-coordinate transition-metal species, i.e., metal species with coordination numbers of less than 4, represent a category of ubiquitous reactive intermediates in metal-catalyzed reactions that take place in solution, in metalloenzymes, on supported nanomaterials and single-atom catalysts, and so on. While reactive intermediates are usually transient and hard to isolate, which makes detailed investigation challenging, molecular representatives of low-coordinate transition-metal intermediates can be synthesized by the judicious use of supporting ligands, allowing detailed study of their inherent chemical and physical properties. By the use of bulky nitrogen- and oxygen-based anionic ligands, plenty of three- and two-coordinate group 4-10 metal complexes with the oxidation states of the metal centers being +3, + 2, and +1 have been prepared and subjected to extensive study. Much less known are low-coordinate zero-valent metal complexes, and knowledge about them had been restricted to group 10 metal complexes until very recently. In this Account, we summarize the studies of the synthesis, spectroscopic features, electronic structures, and reactivities of three-coordinate formal cobalt(0), iron(0), and manganese(0) complexes with persistent carbene and alkene ligation. The introduction of the π-accepting alkene ligands 1,3-divinyl-1,1,3,3-tetramethyldisiloxane (dvtms) and vinyltrimethylsilane (vtms) into the reduction reactions of MCl2 (M = Co, Fe, Mn) with persistent carbenes and alkaline metals effectively suppresses ligand C-H bond activation reactions, leading to the successful preparation of three-coordinate formal cobalt(0), iron(0), and manganese(0) complexes LM(η2:η2-dvtms), LM(η2-vtms)2, and L2M(η2-vtms) (M = Co, Fe, Mn; L = N-heterocyclic carbene (NHC), cyclic (alkyl)(amino)carbene (cAAC)). These three-coordinate metal complexes feature pronounced back-donation from the filled metal 3d orbitals to the alkene π* orbital(s), resulting in electronic configurations of (dxy+πalkene*)2(dx2-y2+π'alkene*)2(dz2,dxz,dyz)n (the coordination plane was chosen as the xy plane; n = 5, 4, and 3 for Co, Fe, and Mn, respectively) for the bis(alkene) complexes LM(η2:η2-dvtms) and LM(η2-vtms)2. The alkene ligands in the low-coordinate formal zero-valent metal complexes are amenable to undergo ligand-exchange reactions with better π-accepting ligands. In reactions with organic azides, hydrosilanes, nitrosoarenes, alkynes, etc., the alkene ligands dissociate from the metal coordination sphere, and three-coordinate formal zero-valent metal complexes function as synthons of LnM0 (L = NHC, cAAC; n = 1, 2; M = Co, Fe, Mn) to perform redox reactions with these substrates, affording divalent and tetravalent cobalt, iron, or manganese complexes. These electronic structure and reactivity features hint at the potential of low-coordinate zero-valent group 7-9 metal complexes for the development of new 3d metal catalysts and magnetic materials.