A three-coordinate cobalt(I) complex exhibits high catalytic efficiency and selectivity as well as good functional group compatibility in alkyne hydrosilylation. [Co(IAd)(PPh3)(CH2TMS)] (1) (IAd = 1,3-diadamantylimidazol-2-ylidene) facilitates regio- and stereoselective hydrosilylation of terminal, symmetrical internal, and trimethylsilyl-substituted unsymmetrical internal alkynes to produce single hydrosilylation products in the forms of β-(E)-silylalkenes, (E)-silylalkenes, and (Z)-α,α-disilylalkenes, respectively, in high yields. The comparable catalytic efficiency and selectivity of the Co(I) silyl complex [Co(IAd)(PPh3)(SiHPh2)] that was prepared from the reaction of 1 with H2SiPh2, and the isolation of an alkyne Co(I) complex [Co(IAd)(η(2)-PhC≡CPh)(CH2TMS)] from the reaction of 1 with the acetylene, point out a modified Chalk-Harrod catalytic cycle for these hydrosilylation reactions. The high selectivity is thought to be governed by steric factors.

Intramolecular C(sp 3 )−H bond activation reactions mediated by low-valent cobalt, both Co(I) and Co(0), have been observed in the reactions of the three-coordinate cobalt complex [Co(IMes) 2 Cl] (IMes = 1,3-dimesitylimidazol-2-ylidene) with alkylation reagents and sodium amalgam. The reactions with alkylation reagents gave [Co(IMes)(IMes′)(N 2 )], featuring a metalated IMes′ anion, whereas the oneelectron-reduction reaction afforded [Co(IMes′) 2 ]. The Co(II) complex can react with CO, isocyanide, and a diazo compound to furnish interesting cobalt complexes bearing functionalized N-heterocyclic carbene ligands. The establishment of these conversions demonstrates the capability of low-valent cobalt with coordination unsaturation to mediate C(sp 3 )−H bond activation and functionalization.

A series of single component FLPs has been investigated for small molecule capture, with the finding that through tuning of both the thermodynamics of binding/activation and the degree of preorganization (i.e., ΔS(⧧)) reversibility can be brought about at (or close to) room temperature. Thus, the dimethylxanthene system {(C6H4)2(O)CMe2}(PMes2)(B(C6F5)2): (i) heterolytically cleaves dihydrogen to give an equilibrium mixture of FLP and H2 activation product in solution at room temperature and (ii) reversibly captures nitrous oxide (uptake at room temperature, 1 atm; release at 323 K).

The catalytic dehydrogenation of ammonia- and amine-boranes by a dimethylxanthene-derived frustrated Lewis pair is described. Turnover is facilitated on a thermodynamic basis by the ready release of H2 from the weakly basic PPh2-containing system. In situ NMR studies and the isolation of intermediates from stoichiometric reactions support a mechanism initiated by B-H activation, followed by end-growth BN coupling involving the terminal NH bond of the bound BN fragment and a BH bond of the incoming borane monomer.