Octahedrally coordinated cobalt(II) complexes with ar edox-active bisguanidine ligand and acac co-ligands were synthesized and their redoxc hemistry analysed in detail. The N À Hfunctions in abisguanidine ligand with partially alkylated guanidino groups form N À H•••O hydrogen bonds with the acac co-ligands,t hereby massively influencing the redox chemistry. Fora ll complexes,t he first one-electron oxidation is metalcentred, leading to Co III complexes with neutral bisguanidine ligand units.Further one-electron oxidation is ligand-centred in the case of Co-bisguanidine complexes with fully alkylated guanidino groups,g iving Co III complexes with radical monocationic bisguanidine ligands.O nt he other hand, the hydrogen-bond strengthening upon oxidation of the Co-bisguanidine complex with partially alkylated guanidino groups initiates metal reduction (Co III !Co II )and two-electron oxidation of the guanidine ligand, providing the first example for the stimulation of redox-induced electron transfer by interligand hydrogen bonding.