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However, the isosbestic point that appears during the evolutio of Spectrum A is less clearly seen at this PH. Moreover, the stable isomer of [PMoW
$_11$ O$_40$ ]$^{4-}$ is believed to disproportionate at PH${\ge}$ 2. See Reference 2. These are the reasons why we present the spectra at PH 1.1 in Figures 1 and 2. -
The molybdenum complexes that contribute to Spectrum A at 20.2 kK and their molar abso(
${\varepsilon}$${\varepsilon}$ >3040). Complex B ((${\varepsilon}$ 980). and[Mo($_2$ O$_4$ (PW($_{11-}$ O($_39$ )$_2$ ]($^{12-}$ (${\varepsilon}$ /2<170 dm>$^3$ mol>$^{-1}$ cm$^{-1}$ ). The last comples is discussed later in the text.