Mononuclear nonheme manganese(IV)-oxo complexes binding calcium ion and other redox-inactive metal ions, [(dpaq)mn(IV)(O)]M-+(n+) (1-Mn+, Mn+ = Ca2+, Mg2+, Zn2+, Lu3+, Y3+, Al3+, and Sc3+) (dpaq = 2-[bis(pyridin-2-ylmethyl)]amino-N-quinolin-8-yl-acetamidate), were synthesized by reacting a hydroxomanganese(III) complex, [(dpaq)Mn-III(OH)](+), with iodo-sylbenzene (PhIO) in the presence of redox-inactive metal ions (Mn+). The Mn(IV)-oxo complexes were characterized using various spectroscopic techniques. In reactivity studies, we observed contrasting effects of Mn+ on the reactivity of 1-Mn+ in redox reactions such as electron-transfer (ET), oxygen atom transfer (OAT), and hydrogen atom transfer (HAT) reactions. In the OAT and ET reactions, the reactivity order of 1-Mn+, such as 1-Sc3+ approximate to 1-Al3+ > 1-Y3+ > 1-Lu3+ > 1-Zn2+ > 1-Mg2+ > 1-Ca2+, follows the Lewis acidity of Mn+ bound to the Mn-O moiety; that is, the stronger the Lewis acidity of Mn+, the higher the reactivity of 1-Mn+ becomes. In sharp contrast, the reactivity of 1-Mn+ in the HAT reaction was reversed, giving the reactivity order 1-Ca2+ > 1-Mg2+ > 1-Zn2+ > 1-Lu3+> 1-Y3+> 1-Al3+ approximate to 1-Sc3+; that is, the higher is Lewis acidity of Mn+, the lower the reactivity of 1-Mn+ in the HAT reaction. The latter result implies that the Lewis acidity of Mn+ bound to the Mn-O moiety can modulate the basicity of the metal-oxo moiety, thus influencing the HAT reactivity of 1-Mn+; cytochrome P450 utilizes the axial thiolate ligand to increase the basicity of the iron-oxo moiety, which enhances the reactivity of compound I in C-H bond activation reactions.