Keller R J, Rush J D, Grover T A
UAMS Division of Toxicology, Little Rock 72205.
J Inorg Biochem. 1991 Mar;41(4):269-76. doi: 10.1016/0162-0134(91)80019-e.
Complexes of vanadium(IV), vanadyl, are reported to be formed with the trihydroxamic acid deferoxamine (H3DF+). One complex exhibits a reddish-violet color, with a major absorbance peak at 386 nm and a smaller peak at 520 nm. This complex is potentially useful for the microdetermination of vanadyl. The apparent molar absorptivity is 3.91 mM-1 cm-1, and the complex obeys Beer's law in the concentration range of 0.6-63 ppm. Electron spin resonance studies indicate the formation of two vanadyl complexes that are 1:1 in vanadyl and deferoxamine, but have two or three bound hydroxamate groups. ESR and spectrophotometric evidence indicate that the red, low pH form, involves an octahedral vanadium (4+) ion coordinated by three hydroxamate ligands. One of these hydroxamates is displaced by an oxygen at pH greater than 2.8 according to the following equilibria: VO2+ + H3DF+ in equilibrium with VIV(DF)2+ + H3O+, VIV(DF)2+ + H2O in equilibrium with VO(HDF)+ + H+, where pk2 = 2.8.
据报道,钒(IV)即氧钒根离子能与三异羟肟酸去铁胺(H3DF+)形成配合物。其中一种配合物呈现红紫色,在386nm处有一个主要吸收峰,在520nm处有一个较小的峰。这种配合物可能对微量测定氧钒根离子有用。其表观摩尔吸光系数为3.91 mM-1 cm-1,该配合物在0.6 - 63 ppm的浓度范围内符合比尔定律。电子自旋共振研究表明形成了两种钒氧配合物,它们中钒氧根离子与去铁胺的比例为1:1,但有两个或三个结合的异羟肟酸基团。电子自旋共振和分光光度法证据表明,红色的低pH形式涉及由三个异羟肟酸配体配位的八面体钒(4+)离子。根据以下平衡,在pH大于2.8时,其中一个异羟肟酸基团会被一个氧取代:VO2+ + H3DF+ 与 VIV(DF)2+ + H3O+ 处于平衡,VIV(DF)2+ + H2O 与 VO(HDF)+ + H+ 处于平衡,其中pK2 = 2.8。