The stability constants of ML-type complexes of the two linear triphosphate ligand anion analogues triphosphate (\documentclass[12pt]{minimal}
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\begin{document}$$ {\text{P}}_{ 3} {\text{O}}_{10}^{5 - } $$\end{document}) and diimidotriphosphate (\documentclass[12pt]{minimal}
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\begin{document}$$ {\text{P}}_{ 3} {\text{O}}_{ 8} ( {\text{NH}})_{2}^{5 - } $$\end{document}) were investigated thermodynamically using potentiometric titrations according to Schwarzenbach’s procedure. The stability constants of the ML-type complexes of different divalent metal ions with \documentclass[12pt]{minimal}
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\begin{document}$$ {\text{P}}_{ 3} {\text{O}}_{ 8} ( {\text{NH}})_{2}^{5 - } $$\end{document} are larger than those of the corresponding complexes with \documentclass[12pt]{minimal}
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\begin{document}$$ {\text{P}}_{ 3} {\text{O}}_{10}^{5 - } $$\end{document} because of the greater basicity of the imino group. The order of the stability constants for the ML-type complexes follows the Irving–Williams order, indicating that only non-bridging oxygen atoms are coordinated directly to the different metal ions in both ligands, and that the imino groups cannot participate in coordination to the metal ions. In the complexation reactions of the Ca2+, Sr2+, Ba2+–\documentclass[12pt]{minimal}
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\begin{document}$$ {\text{P}}_{ 3} {\text{O}}_{10}^{5 - } $$\end{document} and Cu2+, Zn2+, Ni2+–\documentclass[12pt]{minimal}
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\begin{document}$$ {\text{P}}_{ 3} {\text{O}}_{ 8} ( {\text{NH}})_{2}^{5 - } $$\end{document} systems, each metal ion forms an enthalpically stable complex, and there was no suggestion of a conspicuous entropic effect based on the chelate effect. Monodentate complexes that are strongly coordinated with the ligands were there...