The one-pot reaction of CoCl2 with 1 or 2 equiv of N-heterocyclic carbene (NHC) ligands, vinyltrimethylsilane (vtms), and 2 equiv of reducing reagents (KC8 or Na(Hg)) proved an effective protocol for the synthesis of three-coordinate NHC-cobalt(0)-olefin complexes, and by which the new low-coordinate cobalt(0) complexes [(NHC)Co(vtms)(2)] (NHC = 1,3-di(2',6'-diethylphenyl)-4,5-(CH2)(4)-imidazol-2-ylidene (cyIDep), 6; 1,3-diadamantylimidazol-2-ylidene (IAd), 7) and [(NHC)(2)Co(vtms)] (NHC = 1-(2',4',6'-trimethylphenyl)-3-cyclohexylimidazol-2-ylidene (IMesCy), 8; 1,3-dicyclohexylimidazol-2-ylidene (ICy), 9) were prepared in moderate yields and further characterized by spectroscopic methods. The NHC-cobalt(0)-vtms complexes can serve as low-coordinate NHC-cobalt(0) precursors to react with hydrosilanes. From the reactions of Ph2SiH2 with the corresponding NHC-cobalt(0)-vtms complexes, the cobalt silyl complexes [(cyIDep)(H)Co(mu-eta(2):eta(2)-H2SiPh2)(mu-eta(2)-HSiPh2)(2)Co(H)(cyIDep)] (10), [(NHC)Co(mu-eta(2)-SiHPh2)(2)Co(NHC)] (NHC = IPr, 13; IAd, 14), and [(IMesCy)(2)Co(H)(SiHPh2)] (15) were synthesized. Further reactivity studies established the thermal decomposition of 10 to give [(cyIDep)Co(mu-eta(2)-HSiPh2)(2)Co(cyIDep)] (11), H-2, and Ph2SiH2, the reaction of 11 with ButNC (4.5 equiv) to afford [(cyIDep)(ButNC)Co(mu-eta(2)-HSiPh2)(2)Co(CNBut)(3)] (12) and cyIDep, as well as the conversion of 15 to a silyl-functionalized NHC-cobalt(II) complex 16 upon eliminating H-2. These cobalt silyl complexes have been characterized by single-crystal X-ray diffraction studies, NMR, absorption, and infrared spectroscopies, as well as elemental analyses. The diversified reaction outcomes demonstrate the rich reaction chemistry of low-coordinate NHC-cobalt(0) complexes.