Bimetallic homonuclear iron(II) and ruthenium(II) N-heterocyclic carbene complexes have been synthesized and crystallographically analyzed. As a spacer ligand for interconnecting the two redox-active metal centers, a ditopic carbene ligand has been used that comprises two carbene sites annelated to benzene. Detailed electrochemical and spectroelectrochemical analyses of the bimetallic systems revealed that despite the potentially pi-delocalized nature of the ditopic ligand, the iron centers are only moderately coupled. In the ruthenium complexes, the intermetallic interactions are very weak and the centers are electrochemically nearly independent. A model is proposed for rationalizing these observations which is based on (I) relatively weak charge delocalization in the spacer ligand and (II) on electrostatic factors governing the metal-carbene bond.