Since [Sn 8 ] 6À was discovered from the solid-state phase in 2000, its solution chemistry has been elusive due to the high charges and chemical activity. Herein, we report the synthesis and characterization of an inverse sandwich-type cluster dimer {[K 2 ZnSn 8 (ZnMes)] 2 } 4À (1 a), in which the highly charged [Sn 8 ] 6À is captured by mixed-valence Zn I /Zn II to form the dimer {closo-[Zn 2 Sn 8 ]} 2 moieties bridged by a Zn-Zn bond. Such Zn-Sn cluster not only exhibits a novel example of mixedvalence Zn I /Zn II for stabilizing highly active anion species, but also indicates the [Sn 8 ] 6À cluster can act as a novel bridging ligand, like arene, with a h 4 :h 4 -fashion. Theoretical calculations indicate that a significant delocalization of electrons over Zn atoms plays a vital role in the stabilization of the [Sn 8 ] 6Àspecies. The AdNDP and magnetic response analyses clearly showed the presence of local s-aromaticity in three cluster fragments: two ZnSn 4 caps and Sn 8 square antiprism.