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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Vanadium complexes with multidentate amine bisphenols
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Vanadium complexes with multidentate amine bisphenols

机译:钒与多齿胺双酚的络合物

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The reaction of VO(acac)_2 (acac~? = acetyl acetonate) with tripodal glycine bisphenol H_3L~1 under an ambient atmosphere yields a hexacoordinated vanadium(IV) complex [V(acac)(L~1)] (1). The corresponding reactions with tripodal 2-propanolamine bisphenol H_3L~2 and potentially pentadentate ethoxyethanolamine bisphenol H_3L~3 lead to the oxidation of the metal centre and formation of mononuclear oxovanadium(V) complexes [VO(L~2)] (2) and [VO(L~3)] (3), respectively. Alternatively, these latter two complexes can be prepared using VOSO_4·5H_2O or VO(OPr)_3 as a precursor. The CV of 1 in an ACN solution shows a reversible one-electron process at E_(1/2) = +1.18 V, whereas 2 and 3 have an irreversible redox response at ?1.6 V and ?1.2 V, respectively. Complexes 2 and 3 show moderate activity in the epoxidation of cis-cyclooctene by tert-BuOOH at 50 ℃.
机译:在环境气氛下,VO(acac)_2(acac〜?=乙酰丙酮)与三脚架甘氨酸双酚H_3L〜1的反应生成六配位钒(IV)络合物[V(acac)(L〜1)](1)。与三脚架2-丙醇胺双酚H_3L〜2和潜在的五齿乙氧基乙醇胺双酚H_3L〜3的相应反应导致金属中心氧化并形成单核氧钒(V)络合物[VO(L〜2)](2)和[ VO(L〜3)](3)。或者,可以使用VOSO_4·5H_2O或VO(OPr)_3作为前体制备后两种配合物。在ACN溶液中,CV为1时,在E_(1/2)= +1.18 V时显示出可逆的单电子过程,而2和3分别在?1.6 V和?1.2 V时具有不可逆的氧化还原响应。配合物2和3在50℃的叔丁基OOH中对顺环辛烯的环氧化反应具有中等活性。

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