We report a new family of inorganic ligands, namely, transition metal-based thiometallates, for the surface functionalization of colloidal nanocrystals (NCs). We synthesized Pt-, Fe-, Co-, and Ni-based thiometallates, in which transition metal ions were complexed with polysulfides. These inorganic anions easily exchanged the surface organic ligands of various nanocrystals of metal, semiconductor, and oxide materials, without affecting the NCs' primary structural and optical characteristics. Furthermore, upon heating, these complexes were decomposed and transformed into crystalline phases of metal sulfides or pure metals, accompanied by the evaporation of S. Based on this effect, we selectively synthesized homogeneously distributed atomic Pt clusters or Pt nanoparticles on Fe 3 O 4 nanomaterials by heating thioplatinatecapped Fe 3 O 4 NCs. As a model application, we tested the prepared Ptfunctionalized Fe 3 O 4 nanomaterial as a heterogeneous catalyst for CO oxidation reaction and Pt−Fe 3 O 4 catalysts exhibited the high turnover frequency due to the homogeneous distribution of atomic Pt over Fe 3 O 4 and the corresponding strong metal−support interaction. This approach opens up a new avenue to functionalize nanocrystals for catalytic applications.