“…Furthermore, it has been suggested that the molybdenum cations [28] as well as the vanadium cations [29,30] migrate from the Keggin anion to cationic positions in the structure [31,32] and that the heteropoly acids become partially reduced under reaction conditions [33,34]. This migration of cations from the Keggin anion has been speculated to be responsible for the catalytic activity of the heteropoly oxomolybdates with Keggin structure [25,29,30,33,35,36,37]. The result of the migration is a cubic molybdenum autosalified heteropolyacid (Pn-3m, a = 11.853 Å) derived from triclinic H 3 [PMo 12 O 40 ]*13H 2 O under reduction conditions with propene and hydrogen at temperatures above 600 K. This way the in situ studies on the electronic structure of the active state of HPA are corroborated by direct in situ geometric structural studies using Xray diffraction and EXAFS.…”