Bis(η(5)-2,4-dimethylpentadienyl)ruthenium(II), [(η(5)-C7H11)2Ru] (1, “open ruthenocene”), which has become accessible in high yield and large quantities via an isoprene-derived diallyl ruthenium(IV) complex, can be converted into the protonated open ruthenocene 2 by treatment with HBF4 and subsequently into the protonated half-open ruthenocene 3 by reaction with cyclopentadiene. The electronic structure of 3 was studied by DFT methods, revealing that the CH-agostic complex [(η(5)-C5H5)Ru{(1-4η)-C7H12-η(2)-C(5),H(5)}]BF4 (A) represents the global minimum, which is 3.7 kcal mol(−1) lower in energy than the hydride complex [(η(5)-C5H5)RuH(η(5)-C7H11)]BF4 (B). 2 and 3 were treated with the ligands N,N′-bis(1,3,4,5-tetramethylimidazolin-2-ylidene)-1,2-ethanediamine (BL(Me)) and N,N′-bis(1,3-diisopropyl-4,5-dimethylimidazolin-2-ylidene)-1,2-ethanediamine (BL(iPr)) to afford the cationic 16-electron pentadienyl and cyclopentadienyl complexes [(η(5)-C7H11)Ru(BL(R))]BF4 (4a, R = Me; 4b, R = iPr) and [(η(5)-C5H5)Ru(BL(R))]BF4 (5a, R = Me; 5b, R = iPr). All complexes catalyse the transfer hydrogenation of acetophenone in isopropanol, and the most active complex 4a in this reaction was employed for the hydrogenation of a broader range of aliphatic and aromatic ketones.