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{"title":"Synthesis, Crystal Structure of Tetra-Nuclear Macrocyclic Zn(II) Complex and Its Application as Catalyst for Oxidation of Benzyl Alcohol","authors":"L. Wang, Zi-Jian Wang, Meili Zhao, X. Tai, Jiangyong Ouyang, Yun-fei Li, Wei Zhang, Wenbin Jia","doi":"10.9767/bcrec.16.4.10978.839-846","DOIUrl":null,"url":null,"abstract":"A new six coordinated tetra-nuclear macrocyclic Zn(II) complex, ZnL4(Phen)2 (1) (HL= 3-bromo-2-hydroxybenzaldehyde-pyridine-2-carbohydrazone, Phen = 1,10-phenanthroline) has been synthesized by the self-assembly of 3-bromo-2-hydroxybenzaldehyde-pyridine-2-carbohydrazone, Zn(CH3COO)2•2H2O, NaOH and 1,10-phenanthroline in water/ethanol (v:v = 1:3) solution. Complex 1 was characterized by elemental analysis, infra red (IR), and single-crystal X-ray diffraction (XRD) analysis. The results show that Zn1 and Zn1b ions are six-coordinated with a distorted octahedral geometric configuration by four O atoms of two different L ligands and two N atoms of two different L ligands, Zn1a and Zn1c ions are also six-coordinated with a distorted octahedral geometric configuration by two N atoms of two different L ligands, two N atoms of Phen ligands and two O atoms of two different L ligands. Complex (1) forms 3D network structure by the - interaction. The selective oxidation reactions of benzyl alcohols catalyzed by complex (1) was investigated. The highest benzyl alcohol conversion and benzaldehyde selectivity were obtained at 100 °C for 4 h under 5 bar of O2. Copyright © 2021 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). ","PeriodicalId":46276,"journal":{"name":"Bulletin of Chemical Reaction Engineering and Catalysis","volume":" ","pages":""},"PeriodicalIF":1.3000,"publicationDate":"2021-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of Chemical Reaction Engineering and Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9767/bcrec.16.4.10978.839-846","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
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四核大环Zn(II)配合物的合成、晶体结构及其在苯甲醇氧化催化剂中的应用
在水/乙醇(v:v=1:3)溶液中,由3-溴-2-羟基苯甲醛吡啶-2-碳腙、Zn(CH3COO)2•2H2O、NaOH和1,10-菲咯啉自组装,合成了一种新的六配位四核大环Zn(II)配合物ZnL4(Phen)2(1)(HL=3-溴-2-羟基苯甲醛吡啶-2-甲腙,Phen=1,10-菲咯啉)。通过元素分析、红外光谱(IR)和单晶X射线衍射(XRD)对配合物1进行了表征。结果表明,Zn1和Zn1b离子是由两个不同L配体的四个O原子和两个不同的L配体的两个N原子以扭曲的八面体几何构型六配位的,两个Phen配体的N原子和两个不同L配体的O原子。复合体(1)通过相互作用形成三维网络结构。研究了配合物(1)催化苯甲醇的选择性氧化反应。苯甲醇转化率和苯甲醛选择性最高,在100°C、5巴O2下保持4小时。版权所有©2021作者所有,BCREC集团出版。这是CC BY-SA许可证下的开放访问文章(https://creativecommons.org/licenses/by-sa/4.0)。
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