“…This is especially clear if one looks at the published crystal structures of 1,3-dialkylimidazolium chlorometallates, an especially well-investigated subset of halometallate ILs. Many such structures are reported for divalent metal ions including Cr, Cu, − Co, ,, Fe, , Ge, Hg, Mn, Ni, , Pb, Pd, ,− Pt, Sn, , and Zn. , In addition to the well-studied [AlCl 4 ] − systems, crystal structures are known for chlorometallates of trivalent Au, , Bi, Ce, , Dy, Er, , Eu, , Fe, − Gd, La, , Nd, Pr, Sb, Sc, Sm, , Y, and Yb . However, for tetravalent metal ions, the list is restricted to just Ge, Ir, Pt, Sn, Ti, − U, V, and Zr, ,,− for pentavalent ions only Np, and Nb, , and for hexavalent ions only U and Mo. , This may reflect how the weakly coordinating ions found in many commonly used ILs cannot dissolve salts of highly charged ions.…”