The reactivity of the organotin sulfide clusters [(R 1 Sn) 3 S 4 Cl] (A, R 1 = CMe 2 CH 2 COMe) and [(R 1 Sn) 4 S 6 ] (B) towards different zinc chloride phosphane complexes [ZnCl 2 (PR 3 ) 2 ] as well as diphenylzinc ZnPh 2 was investigated. A diversity of different reaction products was obtained. In reactions starting from A, the tin sulfide cluster core was retained as a cation upon release of the chloride ligand, but side reactions occurred that yielded various chlorostannate or chlorozincate anions to crystallize along with the cations in the salts [(R 2 Sn) 3 S 4 ][SnCl 3 ] (1, R 2 = CMe 2 CH 2 C(NNH 2 )Me), [(R 3 Sn) 3 S 4 ] 2 -[dppe(ZnCl 3 ) 2 ] (2, R 3 = CMe 2 CH 2 (NNHPh)Me), and [(R 2 Sn) 3 S 4 ] 2 - [a]