Related Products of 3153-26-2, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 3153-26-2, Name is Vanadyl acetylacetonate,introducing its new discovery.
[VO(acac)2] reacts with HL (HL is the hydrazone Hacpy-inh I, or Hacpy-bhz II; acpy = acetylpyridine, inh = isonicotinic acid hydrazide, bhz = benzoylhydrazide) in dry methanol to yield the oxovanadium(IV) complexes [VOL(acac)] (HL = I: 1, HL = II: 3). The dioxovanadium(v) complexes [VO2L] (HL = I: 2, HL = II: 4) are obtained by aerial oxidation of 1 and 3 in methanol. Treatment of 1 and 3, or 2 and 4, with H2O2 yields the oxoperoxovanadium(v) complexes [VO(O2)L] (HL = I: 5, HL = II: 6). In the presence of catechol or benzohydroxamic acid, 1 and 3 give the mixed chelate complexes [VOL(cat)] (HL = I: 7, HL = II: 8) or [VOL(bha)] (HL = I: 9, HL = II: 10). The peroxo complexes 5 and 6 undergo oxygen transfer reaction with PPh3 in DMF. In DMF and DMSO, 7, 8, 9 and 10 slowly convert to the corresponding dioxo species 2 and 4. Acidification of 2 and 4 with HCl dissolved in methanol affords oxo-hydroxo complexes. Reaction of 7 with L-ascorbic acid yields 2. The crystal and molecular structures of 2 and 4 have been determined, confirming the ONN binding mode of I and II from their enolate form.
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Reference:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI