The reaction of dialane (dpp-Bian)Al−Al(dpp-Bian) (1) (dpp-Bian is dianion of 1,2-bis [(2,6diisopropylphenyl)imino]-acenaphthene) with 1 mol equiv of 1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene (iPr 2 Im Me ) results in the Al-carbene adduct (dpp-Bian)(iPr 2 Im Me )Al− Al(dpp-Bian) (3). In the course of the reaction of dialane 1 with 2 mol equiv of 1,3-diisopropyl-4,5-dimethylimidazol-2thione (iPr 2 Imt Me ) a half of the thione amount undergoes a cleavage of sulfur−carbon double bond. In the product (dpp-Bian)(iPr 2 Im Me )Al(μ-S)Al(iPr 2 Imt Me )(dpp-Bian) (4) aluminum atoms coordinate carbene as well as thione ligands. Compound 4 is thermally robust: no reduction of CS bond in thione moiety by the dpp-Bian ligands could be observed in toluene for 24 h at 100 °C. Complex {(dpp-Bian)(iPr 2 Im Me )Al} 2 (μ-S) (5) was isolated from the reaction of dialane 1, iPr 2 Im Me , and iPr 2 Imt Me (1:1:1). The reaction of mononuclear (dpp-Bian)AlH(THF) (2) (THF = tetrahydrofuran) affords compound (dpp-Bian)AlH(iPr 2 Im Me ) (6). Compounds 3−6 were characterized by 1 H NMR and IR spectroscopy; their molecular structures were established by single-crystal X-ray analysis.