Transition-metal-centered monocyclic boron wheel clusters (M (c) B-n(q)) represent a family of interesting borometallic compounds with double aromaticity. A variety of early and late transition metal atoms have been found to form such structures with high symmetries and various B-n ring sizes. Here we report a combined photoelectron spectroscopy and quantum-chemistry theoretical study of two MOB clusters from the middle of the transition metal series: Re (c) B-8(-) and Re (c) B-9(-). Global minimum structure searches revealed that ReB8- adopts a pseudo-C-8v, structure while ReB9- is a perfectly planar D-9h molecular wheel. Chemical bonding analyses showed that both clusters exhibit sigma and pi double aromaticity and obey the electronic design principle for metal-centered borometallic molecular wheels. The central Re atoms are found to possess unusually low oxidation states of +I in Re (c) B-8(-) and +II in Re (c) B-9(-), i.e., the Re atom behaves similarly to late transition metal elements (Ru, Fe, Co, Rh, Ir) in the M (c) B-n(-) molecular wheels. These two clusters become new members of the family of transition-metal-centered monocyclic borometallic molecular wheels, which may be viable for chemical syntheses with appropriate ligands.