Trinuclear titanium complexes coordinated by one ligand with three coordination sites have shown properties of mixed valency and a high number of reversible redox steps. Herein we report on the hexaphenyl-substituted derivative (Cp2Ti)(3)(mu(3)-HATNPh(6)) (2). On reaction of 2 with the ferrocenium salt [Cp2Fe]BF4, the cationic complexes [(Cp2Ti)(3) (mu(3)-HATNPh(6))](n+) (n = 1-3; 3-5) become available in a selective way. Cyclic voltammograms show 10 reversible redox states of the trinuclear species 2 without decomposition. In order to classify the degree of electronic communication between the titanium centers, comproportionation constants K-c, IVCT bands in NIR spectra, and magnetic measurements were analyzed. These parameters show strong coupling effects between the titanium centers but no full delocalization. In addition, single-crystal X-ray analysis of the neutral complex 2 and its oxidation products (1+ (3), 2+ (4), and 3+ (5)) revealed the geometric structure of the molecule in the solid state. For the cationic species anion-pi interactions between the electron-deficient central ring of the HATNPh(6) ligand and BF4- counterions were found.