We describe herein the synthesis of a germylene-β-sulfoxide ligand, 1, and its abilities in coordination chemistry. Treatment of 1 with metal complexes [W(cod)(CO)4], [Mo(nbd)(CO)4] and [Ni(cod)2] afforded the corresponding (1)-chelated metal complexes (1)-W(CO)4 (2a), (1)-Mo(CO)4 (2b), and (1)-Ni(cod) (4a), clearly showing a bidentate ligation of the metal by the germanium(II) and sulfur centers. Coordination with [Ru(PPh3)3Cl2] afforded an unprecedented bridged bis(ruthenium) complex 3b. In the case of 4a, the hemilability of the bidentate ligand 1 was demonstrated by sulfoxide substitution by a CO ligand.