“…1, 9 During the past few decades, owing to the diversity of the bonding modes of the chalcogen atoms, the stereochemical effect of the lone electron pairs and the various coordination orientations of As/Sb(III) by sulfur/ selenium atoms, large structural and compositional diversities have been observed for multinary chalcogenides, and therefore a large number of metal chalcogenides compounds have been prepared. Recently, it has been reported that in the combination of the structural units of As x Q y (Q ¼ S, Se) the As III ions tend to adopt the diverse AsQ n (Q ¼ S, Se) (n ¼ 3-6) ligands that can share corners and/or edges with transition metal ions (TM ¼ Ag + , Cu 2+ , Mn 2+ ), 11,[13][14][15][16][17][18][19][20][21][22][23][24] and could form interesting structural various multinary chalcogenides, 8 such as 1D chains, 2D layers, 3D framework. For example, RbAg 2 As 3 Se 6 , 10 NaAg 2 AsS 3 $H 2 O, 13 (NH 3 CH 2 CH 2 NH 3 )AgAsS 4 , 14 CsAgAs 2 Se 4 , 15 27 From the above instances we can see clearly that it is relatively rare for alkali metals cations used as structural directing agents to contain Hg/Cd arsenic chalcogenides in the M-TM-As-Q (M ¼ alkali metals; TM ¼ Hg, Cd; Q ¼ S, Se) systems.…”