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含三齿腙的二氧化钼(VI)配合物的合成、晶体结构及催化性能

Synthesis, Crystal Structures and Catalytic Property of Dioxidomolybdenum(VI) Complexes with Tridentate Hydrazones.

作者信息

Luo Xiao-Qiang, Han Yong-Jun, Xue Ling-Wei

出版信息

Acta Chim Slov. 2020 Sep;67(3):853-859.

Abstract

New dioxidomolybdenum(VI) complexes with the formula [MoO2L(MeOH)], derived from N'-(5-chloro-2-hydroxy-benzylidene)-2-methylbenzohydrazide (H2L1) and N'-(3,5-dichloro-2-hydroxybenzylidene)-2-methylbenzohydrazide (H2L2) were prepared. Crystal and molecular structures of the complexes were determined by single crystal X-ray dif-fraction method. Both complexes were further characterized by elemental analysis and FT-IR spectra. Single crystal X-ray structural studies indicate that the hydrazones L1 and L2 coordinate to the MoO2 cores through the enolate oxygen, phenolate oxygen and azomethine nitrogen. The Mo atoms in both complexes are in octahedral coordination. Catalytic properties for epoxidation of styrene by the complexes using PhIO and NaOCl as oxidant have been studied.

摘要

制备了通式为[MoO₂L(MeOH)]的新型二氧代钼(VI)配合物,其衍生自N'-(5-氯-2-羟基-亚苄基)-2-甲基苯甲酰肼(H₂L₁)和N'-(3,5-二氯-2-羟基-亚苄基)-2-甲基苯甲酰肼(H₂L₂)。通过单晶X射线衍射法测定了配合物的晶体结构和分子结构。通过元素分析和傅里叶变换红外光谱对两种配合物进行了进一步表征。单晶X射线结构研究表明,腙L₁和L₂通过烯醇盐氧、酚盐氧和偶氮甲碱氮与MoO₂核配位。两种配合物中的Mo原子均为八面体配位。研究了以PhIO和NaOCl为氧化剂时,该配合物对苯乙烯环氧化的催化性能。

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