Liang Min, Sun Nan, Zou Dong-Hui
Acta Chim Slov. 2018 Dec;65(4):964-969.
A pair of new oxidovanadium(V) complexes, [VOL1L]·EtOH (1) and [VOL2L]·EtOH (2) (L = acetohydroxamate), derived from the aroylhydrazones N'-(5-bromo-2-hydroxybenzylidene)-4-methoxybenzohydrazide (H2L1) and N'-(5-bromo-2-hydroxybenzylidene)-4-methylbenzohydrazide (H2L2), have been prepared and characterized by elemental analyses, FT-IR, 1H and 13C NMR spectroscopy and single-crystal structural X-ray diffraction. The complexes have octahedral structures in which the aroylhydrazone ligands behave as binegative donors. Single-crystal structure analyses reveal that the V centers are coordinated by the donor atoms of the aroylhydrazone ligands, the acetohydroxamate ligands and the oxido groups.Crystal structures of the complexes are stabilized by hydrogen bonds. The complexes function as effective olefin epoxidation catalysts.
通过元素分析、傅里叶变换红外光谱(FT-IR)、核磁共振氢谱(1H NMR)、核磁共振碳谱(13C NMR)和单晶结构X射线衍射对由芳酰腙N'-(5-溴-2-羟基亚苄基)-4-甲氧基苯甲酰肼(H2L1)和N'-(5-溴-2-羟基亚苄基)-4-甲基苯甲酰肼(H2L2)衍生得到的一对新型氧化钒(V)配合物[VOL1L]·EtOH(1)和[VOL2L]·EtOH(2)(L = 乙酰氧肟酸)进行了制备和表征。这些配合物具有八面体结构,其中芳酰腙配体作为双负供体。单晶结构分析表明,钒中心由芳酰腙配体、乙酰氧肟酸配体和氧化基团的供体原子配位。配合物的晶体结构通过氢键得以稳定。这些配合物可作为有效的烯烃环氧化催化剂。