The title complex, [Zn(CH5N3S)2(C2H6OS)](C6H2N3O7)2·C2H6OS·H2O, is composed of a [Zn(thio­semi­carbazide)2(DMSO)]2+ cation (where DMSO is dimethyl sulfoxide), and two picrate anions. In the asymmetric unit, there is also a solvent mol­ecule of DMSO and a water mol­ecule of crystallization. In the cation, the ZnII atom is five-coordinated in a distorted square–pyramidal geometry. It coordinates to the O atom of a DMSO mol­ecule and to the S and one N atom of two thio­semicarbazide mol­ecules, which behave as bidentate ligands coordinating in a trans arrangement. In the crystal, a number of N—H⋯O, O—H⋯O and N—H⋯S hydrogen bonds link the mol­ecules into two-dimensional networks. These networks are further linked via weak C—H⋯O inter­actions, forming a three-dimensional arrangement. Positional disorder in one methyl group of the coordinated DMSO molecule and in the two picrate anions was observed.

In the cation of the title compound, [Cd(CH5N3S)2(C2H6OS)2](C6H2N3O7)2·2H2O, the CdII atom is located on an inversion center. It is hexa­coordinated in an octahedral fashion by two thio­semicarbazide mol­ecules, which coordinate in a bidentate manner via the S and N atoms, and to the O atom of two dimethyl sufoxide (DMSO) mol­ecules. The charges are equilibrated by two picrate anions and the complex crystallizes as a dihydrate. In the crystal, these units are linked by a number of O—H⋯O and N—H⋯S hydrogen bonds and weak C—H⋯O inter­actions, forming a three-dimensional network.

In the title compound, [CdI2{(C6H5)3PO}2], the CdII atom is ligated by two I atoms and two O atoms from two triphenyl­phosphine oxide ligands in a disorted tetra­hedral arrangement. While the O—Cd—I angles vary from 106.67 (7) to 111.23 (7)°, the O—Cd—O angle is 88.60 (10)° and the I—Cd—I angle angle is 125.47 (2)°. The crystal structure is stabilized by van der Waals forces only.