6-苯基吡啶-2-羧酸-双(4-吡啶)胺配体三核Zn(II)配合物的合成、晶体结构和催化活性

Lihua Wang, F. Kong, Tai Xi-Shi
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引用次数: 3

摘要

以6-苯基吡啶-2-羧酸、氢氧化钠、双(4-吡啶)胺和Zn(CH3COO)2•2H2O为原料合成了新的三核Zn(II)配合物[Zn3(L1)4(L2)2(CH3COO)2] (1) (HL1 = 6-苯基吡啶-2-羧酸,L2 =双(4-吡啶基)胺)。通过元素分析和x射线单晶衍射对配合物1进行了结构表征。结果表明,配合物1由3个Zn(II)离子、4个L1配体、2个L2配体和2个CH3COO-阴离子组成。在图1中,Zn1离子和Zn1a离子分别与两个不同L1配体的O原子、两个不同L1配体的N原子和一个二(4-吡啶基)胺配体的N原子五配位,形成畸变的三角双金字塔结构。Zn2离子与来自两个不同CH3COO−阴离子的两个O原子和来自两个不同L2配体的两个N原子四配位,形成扭曲的四面体几何形状。配合物1通过分子间的N−H···O氢键呈现出三维网络结构。研究了在温和反应条件下,以配合物1为催化剂对苯甲醇氧化反应的催化性能。结果表明,该催化剂具有很高的活性,以THF为溶剂,在0.5 MPa O2条件下,在90°C条件下,3 h内苯甲醛的收率为50.8%。Copyright©2022 by Authors, Published by BCREC Group。这是一篇基于CC BY-SA许可(https://creativecommons.org/licenses/by-sa/4.0)的开放获取文章。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis, Crystal Structure and Catalytic Activity of Tri-Nuclear Zn(II) Complex Based on 6-Phenylpyridine-2-carboxylic Acid and Bis(4-pyridyl)amine Ligands
A new trinuclear Zn (II) complex, [Zn3(L1)4(L2)2(CH3COO)2] (1) (HL1 = 6-phenylpyridine-2-carboxylic acid, L2 = bis(4-pyridyl)amine) has been synthesized by 6-phenylpyridine-2-carboxylic acid, NaOH, bis(4-pyridyl)amine and Zn(CH3COO)2•2H2O. The complex 1 has also been structural characterized by elemental analysis and single crystal X-ray diffraction. The results reveals that complex 1 is made up of three Zn(II) ions, four L1 ligands, two L2 ligands and two CH3COO- anions. In 1, both Zn1 ion and Zn1a ion are five-coordinated with two O atoms from two different L1 ligands, two N atoms from two different L1 ligands, and one N atoms from bis(4-pyridyl)amine ligand, respectively, and forms a distorted trigonal biyramid geometry. And Zn2 ion is four-coordinated with two O atoms from two different CH3COO− anions and two N atoms from two different L2 ligands, forming a distorted tetrahedral geometry. Complex 1 displays a 3D network structure by the intermolecular N−H···O hydrogen bonds. The catalytic performance for oxidation of benzyl alcohol with O2 was studied under mild reaction conditions using complex 1 as catalyst. The results demonstrated that the catalysts were very active, and the yield of benzaldehyde was 50.8% at 90 °C with THF as solvent under 0.5 MPa O2 within 3 h. Copyright © 2022 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). 
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