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三丁基锡/SBA-15功能配合物的合成、表征及对Friedel-Crafts反应的选择性催化
引用本文:荆涛,覃志乐,宋伟明,赵云鹏,邓启刚.三丁基锡/SBA-15功能配合物的合成、表征及对Friedel-Crafts反应的选择性催化[J].应用化学,2013,30(8):945-950.
作者姓名:荆涛  覃志乐  宋伟明  赵云鹏  邓启刚
作者单位:(齐齐哈尔大学化学与化学工程学院 齐齐哈尔 161006)
基金项目:黑龙江省自然科学基金资助项目,黑龙江省教育厅
摘    要:将三丁基氯化锡与SBA-15介孔分子筛在N2气气氛中进行回流反应,得到有机锡无机配合物(C4H9)3Sn-O-SBA-15Bu3SnS]。 利用X射线衍射(XRD)、透射电子显微镜(TEM)、氮气吸附脱附、固体核磁(NMR)和吡啶吸附脱附红外光谱分析(Py-IR)等方法对产物的组成、结构和性质进行了表征。 结果表明,产物Bu3SnS具有高度有序的六方介孔结构,与SBA-15相比,Bu3SnS比表面积、孔容和孔径变小,酸性增强。 Bu3SnS对苯甲醚Friedel-Crafts酰基化反应具有优异的催化性能,当反应温度为130 ℃,n(苯甲醚)∶n(苯甲酰氯)=1.0∶2.0,w(cat)=6%(相对于苯甲醚用量),反应时间为5 h,苯甲醚的转化率达到76.0%,对甲氧基二苯酮(p-MBP)选择性达到97.8%。

关 键 词:三丁基锡  SBA-15  功能配合物  Friedel-Crafts反应  选择性催化  
收稿时间:2012-12-12
修稿时间:2013-01-26

Synthesis, Characterization and Catalytic Performance Toward the Friedel-Crafts Acylation of Tributyltin Functionalized SBA-15
JING Tao , QIN Zhile , SONG Weiming , ZHAO Yunpeng , DENG Qigang.Synthesis, Characterization and Catalytic Performance Toward the Friedel-Crafts Acylation of Tributyltin Functionalized SBA-15[J].Chinese Journal of Applied Chemistry,2013,30(8):945-950.
Authors:JING Tao  QIN Zhile  SONG Weiming  ZHAO Yunpeng  DENG Qigang
Institution:(College of Chemistry and Chemical Engineering,Qiqihar University,Qiqihar 161006,China)
Abstract:The organotin inorganic complexes (C4H9)3Sn-O-SBA-15Bu3SnS] were successfully synthesized by grafting tributyltin on SBA-15 mesoporous molecular sieves in a nitrogen atmosphere. The composition, structure and properties of the samples were characterized by X-ray diffraction(XRD), transmittance electron microscopy(TEM), Hammett indicator method, N2 adsorption-desorption, solid nuclear magnetic resonance(NMR) , in-situ pyridine infrared spectroscopy(Py-IR) and so on. The results show that the hexagonal P6mm mesostructure of parent siliceous SBA-15 is maintained in Bu3SnS. The surface areas, proe size and volume of Bu3SnS are all deceased with the increase of acidity, compared to those of SBA-15. Friedel-Crafts acylation of anisole and benzoyl chloride can be efficiently catalyzed in the presence of Bu3SnS. The reaction conversion of anisole and the selectivity of p-benzoylanisole are 76.0% and 97.8%, respectively, when the molar ratioof anisole to benzoyl chloride is 0.5∶1.0, the amount of catalyst is 6%, the reaction temperature is 130 ℃ and the reaction time is 5 h.
Keywords:tributyltin  SBA-15  functional complex  Friedel-Crafts reaction  selective catalytsis
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