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水相中Ir-N@C催化的胺和伯醇的N-烷基化反应

Ir-N@C Catalyzed N-alkylation of Amines with Primary Alcohols in Water

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【作者】 王松景志红徐国强牟新东

【Author】 WANG Song;JING Zhi-hong;XU Guo-qiang;MU Xin-dong;Qufu Normal University,College of Chemistry and Chemical Engineering;CAS Key Laboratory of Bio-based Materials,Qingdao Institute of Bioenergy and Bioprocess Technology,Chinese Academy of Sciences;

【机构】 曲阜师范大学化学与化工学院中科院生物基材料重点实验室中科院青岛生物能源与过程研究所

【摘要】 以商品化的活性炭为载体,采用浸渍法制备了稳定、易回收且Ir质量分数为5%的多相催化剂Ir-N@C,考察了不同组分的铱基催化剂、反应温度、反应时间、碱对N-烷基化反应的影响。结果表明,n(Ir)∶n(1,10-Phenanthroline)=1∶2的铱基催化剂,可以在水相中高效催化包括氨水在内的多种胺类与伯醇的N-烷基化反应。运用XRD、TEM、XPS、BET测定手段对催化剂进行了表征。在循环实验中,催化剂体现了较好的稳定性和催化活性,其中,苄醇的转化率为79.1%~92.3%,三苄胺的选择性为74.3%~85.6%。

【Abstract】 A stable,easily recoverable heterogeneous catalyst Ir-N@C( the mass fraction of iridium is5%) was obtained by impregnation with commercial carbon powder. The factors of the N-alkylation reaction including different iridium catalysts,reaction temperature,reaction time and bases were investigated. Experiment results suggested that the N-alkylation of amines with primary alcohols could be efficiently catalyzed in water using iridium catalyst with n( Ir) ∶ n( 1,10-phenanthroline) = 1∶2. The catalyst was characterized by XRD,TEM,XPS,BET. In recycling experiments,the catalyst showed acceptable stability and the catalytic activity. The conversion of benzyl alcohol was 79. 1% ~ 92. 3%,and the selectivity to tribenzylamine was 74. 3% ~ 85. 6%.

【基金】 国家自然科学基金(21273260)~~
  • 【文献出处】 精细化工 ,Fine Chemicals , 编辑部邮箱 ,2015年12期
  • 【分类号】O621.251
  • 【下载频次】128
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