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Ligands play a central role in dictating the electronic properties of metal complexes to which they are coordinated. A fundamental understanding of changes in ligand properties can be used as design principles for more efficient catalysts. Designing ligands that have multiple protonation states that will change the properties of the coordination complex would be useful as potential ways of controlling catalysis, for example, as an on/off switch where one redox state exists below thermodynamic potential and another exists above. Thus, phenol moieties built into strongly coordinating ligands, like that of tpyPhOH (4′-(4-hydroxyphenyl)-2,2′:6′,2′’-terpyridine) may provide such a handle. Herein, we report the electrochemical and spectral characterization, and the crystallographic and computational analysis of two ruthenium analogs: [Ru(tpy)(tpyPhOH)](PF6)2 and [Ru(tpyPhOH)2] (PF6)2 (tpy =2,2′:6′,2′’-terpyridine). Cyclic voltammetry and differential pulse voltammetry indicate that two redox events occur, one of which is pH independent and we hypothesize that these follow an electrochemical- chemical-electrochemical (ECE) mechanism. XRD results of the ruthenium complexes’ protonated forms are generally consistent with expected bond lengths and angles and are in agreement with computational modeling. The properties are compared to a previously reported analog that contains the –OH group directly connected to terpyridine, [Ru(tpyOH)2](PF6)2, where tpyOH is 4′-hydroxy-2,2′:6′,2′’-terpyridine, with some intriguing differences. Overall, these data indicate that the phenyl-substituent decouples the phenol such that it behaves both as an electron withdrawing substituent and a location for a ligand centered oxidation event to occur.