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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Co-ordination of the chiral N, O-ligand 2-[(1S, 2S, 5R)(-)-menthol]-pyridine to molybdenum(VI) and vanadium(IV) oxo complexes Crystal structures of [MoO_2{2-(-)-menthol-pyridine}_2] and [VO{2-(-)-menthol-pyridine}_2]
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Co-ordination of the chiral N, O-ligand 2-[(1S, 2S, 5R)(-)-menthol]-pyridine to molybdenum(VI) and vanadium(IV) oxo complexes Crystal structures of [MoO_2{2-(-)-menthol-pyridine}_2] and [VO{2-(-)-menthol-pyridine}_2]

机译:手性N,O-配体2-[((1S,2S,5R)(-)-薄荷醇]-吡啶与钼(VI)和钒(IV)氧配合物的配位[MoO_2 {2-( -)-薄荷脑吡啶} _2]和[VO {2-(-)-薄荷脑吡啶} _2]

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摘要

Reaction of the chiral 1-pyridin-2-yl-menthol ligand (1) with [VO(acac)_2] and [MoO_2(acac)_2] results in the formation of the metal-oxo complexes [VO(N-O)_2] (2) and [MoO_2(N-O)_2] (3), where N-O = 2-[(-)-menthol]-pyridine. The molecular structures of (2) and (3) have been determined by single-crystal X-ray diffraction, which revealed the expected square-pyramidal geometry for (2) with the pyridine ring nitrogens mutually trans, and the expected slightly distorted octahedral arrangement of (3) with cis di-oxo ligands. Both metal-oxo compounds (2) and (3) have demonstrated the ability to catalyse the asymmetric oxidation of prochiral olefins and sulfides with H_2O_2 or tBuOOH as the oxidant.
机译:手性1-吡啶-2-基-薄荷醇配体(1)与[VO(acac)_2]和[MoO_2(acac)_2]的反应导致形成金属-氧配合物[VO(NO)_2] (2)和[MoO_2(NO)_2](3),其中NO = 2-[(-)-薄荷醇]-吡啶。 (2)和(3)的分子结构已通过单晶X射线衍射确定,揭示了(2)的吡啶环氮互为反式的预期方锥几何形状,以及预期的稍微扭曲的八面体排列(3)具有顺式二-氧代配体。金属-氧代化合物(2)和(3)均已证明能够以H_2O_2或tBuOOH为氧化剂催化前手性烯烃和硫化物的不对称氧化。

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