## Abstract The flash photolysis of the mono and di‐thiocyanate complexes of μ‐oxo __bis__(oxo‐molybdenum(V)) (Mo~2~O~4~(NCS)~__x__~(H~2~O)~6−__x__~^(2−__x__)+^ where __x__ = 1, 2) has been studied in the system composed of perchloric acid solutions of Mo~2~O~4~(H~2~O)~6~^2+^ in the presence of exc
The flash photolysis of di-μ-oxo-bis(oxo-molybdate(V)) acid aqueous solutions in the presence of excess chloride
✍ Scribed by L.S. Villata; M.C. Gonzalez; M.R. Feliz; A.L. Capparelli; S. Signorella
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 835 KB
- Volume
- 69
- Category
- Article
- ISSN
- 1010-6030
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✦ Synopsis
The flash photolysis of di-p-oxo his(oxo-molybdenum(V))
complexes in aqueous solutions of perchloric acid in the presence of excess chloride induced both photolabilization and photo-oxidation of Cl-and/or H,O ligands. Photolabilization produces the formation of reaction intermediates identified as p-oxo-bis (oxo-molybdenum(V)) '+ species: MqO,(p-O)(H,O):+ (A) and M&O+-O)(C1)(HZO), (B). A rapid equilibria between the transient species is established before they decay through a first order reaction. Intermediate A is the only species effective in promoting the observed decay leading to MO(W) and Hz as end products.
The relative absorption spectrum of species B is reported, as well as its stability constant in the temperature range 2545 "C. The effect of ligands on the overall mechanism is discussed.
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