The homoleptic group 5c arbonylates [M(CO) 6 ] À (M = Nb, Ta)s erve as ligands in carbonyl-terminated heterobimetallic Ag m M n clusters containing 3t o1 1m etal atoms. Based on our serendipitous [Ag 6 {Nb(CO) 6 } 4 ] 2 + (4a 2 +)p recedent, we established accesst os uch Ag m M n clusters of the composition [Ag m {M(CO) 6 } n ] x (M = Nb, Ta ; m = 1, 2, 6; n = 2, 3, 4, 5; x = 1À,1+ ,2+). Salts of those molecularc luster ions were synthesized by the reaction of [NEt 4 ][M(CO) 6 ]and Ag[Al(OR F) 4 ](R F = C(CF 3) 3)i nt he corrects toichiometry in 1,2,3,4tetrafluorobenzene at À35 8C. The solid-state structures were determined by single-crystal X-ray diffractionm ethods and, owing to the thermali nstability of the clusters, al imited scope of spectroscopicm ethods. In addition, DFT-based AIM calculations were performed to provide an understanding of the bonding within these clusters. Apparently,t he clusters 3 + (m = 6, n = 5) and 4 2 + (m = 6, n = 4) are superatom complexes with trigonal-prismatic or octahedral Ag 6 superatom cores. The [M(CO) 6 ] À ions then bind through three CO units as tridentate chelate ligands to the superatom core, giving overall structures related to tetrahedral AX 4 (4 2 +)o rt rigonal bipyramidal AX 5 molecules (3 +).