Reaction of the tris-hypersilyl nonagermanide Zintl cluster salt, K[Ge9(Hyp)3] (Hyp=Si(SiMe3)3) with [Rh(η2,η2-L)Cl]2 (L=1,5-cyclooctadiene, COD; norbornadiene, NBD) afforded eleven- and twelve-vertex homo-multimetallic clusters by cluster core expansion. Using a stepwise procedure, starting from the Zintl cluster [Rh(COD){Ge9(Hyp)3}] and [Ir(COD)Cl]2, this methodology was expanded for the synthesis of eleven-vertex hetero-multimetallic clusters. A mechanism for the formation of these first examples of closo eleven-vertex Zintl clusters is proposed, informed by density functional theory calculations.