“…The remaining NH group of N(1) forms a hydrogen bond to the opposite face of the chloride anion and as a result the complex in the solid state forms a centrosymmetric hydrogen-bonded dimer linked by interactions to the chloride anions (Figure 1b). A bidentate, N,S-coordination mode has been seen in a number of deprotonated monothiourea derivatives of ruthenium, [88,89] platinum(II), [90,91] cadmium, [92] zinc, [93] goldA C H T U N G T R E N N U N G (III) [94] and gold(I). [95] The N,S-thioureido chelate binding mode is also observed for complexes with rhenium(V) in a thiol-amide-thiourea ligand, [96] and it is found in both coordinating thioureas for an analogous bis-A C H T U N G T R E N N U N G (thiourea) ligand.…”