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5,7-二溴-8-羟基喹啉锰配合物催化H2O2选择氧化乙苯

Selective Oxidation of Ethylbenzene with Hydrogen Peroxide Catalyzed by 5,7-Dibromo-8-quinolinolato Manganese Complexes

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【作者】 卢春丽伏再辉刘亚纯刘凤兰秦金纬何乡陵尹笃林

【Author】 LU Chun-Li FU Zai-Hui LIU Ya-Chun LIU Feng-Lan QIN Jin-Wei HE Xiang-Ling YIN Du-Lin(Key Laboratory of Resource Fine-Processing and Advanced Materials of Hunan Province,Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research of Ministry of Education of China,College of Chemistry and Chemical Engineering,Hunan Normal University,Changsha 410081,P.R.China)

【机构】 湖南师范大学化学化工学院资源精细化与先进材料湖南省高校重点实验室化学生物学及中药分析教育部重点实验室

【摘要】 设计合成了5,7-二溴-8-羟基喹啉锰的四齿和六齿配合物(Q2MnⅡ和Q3MnⅢ),并用傅里叶变换红外(FT-IR)光谱对两个配合物进行了表征.以醋酸铵和醋酸为助剂,丙酮-水作溶剂,两个锰配合物在室温20℃下能高选择性催化双氧水氧化乙苯制苯乙酮的反应,Q3MnⅢ比Q2MnⅡ具有更高的催化活性和选择性.在优化的反应条件下,乙苯转化率达27%,苯乙酮的选择性>95%;而且催化剂稳定性良好,可循环使用三次.

【Abstract】 Two 5,7-dibromo-8-quinolinolato manganese complexes in tetradentate(Q2MnII) and hexadentate(Q3MnIII) modes were prepared and then characterized by Fourier transform infrared(FT-IR) spectrometry.We found that both Mn complexes,together with NH4OAC and HOAc,efficiently catalyzed the oxidation of ethylbenzene to acetophenone by hydrogen peroxide in an acetone-water medium at 20 ℃.Q3MnIII showed much higher catalytic activity for this reaction than Q2MnII,affording a 27% ethylbenzene conversion and more than 95% selectivity for acetophenone under optimum conditions.Q3MnIII was reused three times without significant deactivation,indicating good stability.

【基金】 国家自然科学基金(20873040,20573035)资助项目~~
  • 【文献出处】 物理化学学报 ,Acta Physico-Chimica Sinica , 编辑部邮箱 ,2010年10期
  • 【分类号】O643.32
  • 【被引频次】7
  • 【下载频次】168
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