The reactivity of Grignard reagents in the presence of nickel catalysts is known to be highly efficient in the deoxydesulfurization of dibenzothiophene sulfone (DBTO 2 ), 4-methyldibenzothiophene (4-MeDBTO 2 ), and 4,6-dimethyldibenzothiophene (4,6-Me 2 DBTO 2 ), to yield sulfur-free biphenyls via cross-coupling reactions. However, the mechanistic details involved in the process remained unknown. In this report the reactivity of [(dippe)Pt(μ-H)] 2 with DBTO 2 turned out to be catalytically less efficient compared with [(dippe)Ni(μ-H)] 2 , but the first allowed the isolation and full characterization of several reaction intermediates, such as [(dippe)Pt(κ 2 -C,S-DBTO 2 )]. It was demonstrated that this is a key intermediate in all the deoxydesulfurization reactions of the above-mentioned aromatic sulfones (DBTsO 2 ).