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苯官能化MCM-41的合成、表征、磺酰化及与二胺的反应
引用本文:聂春发,索继栓. 苯官能化MCM-41的合成、表征、磺酰化及与二胺的反应[J]. 无机化学学报, 2004, 20(6): 641-646
作者姓名:聂春发  索继栓
作者单位:1. 中国科学院兰州化学物理研究所羰基合成与选择氧化国家重点实验室,兰州,730000;解放军第一医院,兰州,730000
2. 中国科学院兰州化学物理研究所羰基合成与选择氧化国家重点实验室,兰州,730000
摘    要:以三乙氧基硅基苯((C2H5O)3Si-Ph,((triethoxysilyl)benzene,TESB)以及正硅酸乙酯(TEOS)的混合液为硅源,以溴代十六烷基吡啶(CPBr)为模板剂,在HCl介质中合成了苯官能化的有机-无机杂化介孔分子筛MCM-41。对合成的分子筛用FT-IR、PXRD、TEM、N2吸附-脱附等手段进行了表征。结果表明,合成的苯官能化的有机-无机杂化介孔分子筛具有良好的介孔孔道结构。用三甲基氯硅烷对分子筛表面的Si-OH进行了封端处理,用氯磺酸对合成的苯官能化的有机-无机杂化介孔分子筛进行了磺酰化,并与各种二胺进行了反应。

关 键 词:介孔分子筛 MCM-41 苯官能化 有机-无机杂化 原位磺酰化
修稿时间:2003-12-16

Benzene Functionalized MCM-41: Synthesis, Characterization, Sulfonylation and Reactions with Diamines
NIE Chun-Fa and SUO Ji-Shuan. Benzene Functionalized MCM-41: Synthesis, Characterization, Sulfonylation and Reactions with Diamines[J]. Chinese Journal of Inorganic Chemistry, 2004, 20(6): 641-646
Authors:NIE Chun-Fa and SUO Ji-Shuan
Affiliation:State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000;The First Hospital of PLA, Lanzhou 730030 and State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000
Abstract:Benzene functionalized organic-inorganic hybrid mesoporous molecular sieve of MCM-41 type was synthesized by co-condensation of (triethoxysilyl)benzene (TESB) and tetraethoxysilane (TEOS) using cetyl pyridine bromide (CPBr) as template. The products were characterized by means of FT-IR, Powder XRD and N2 adsorption/desorption isotherm. The prepared organosilica was with hexagonal structure and mesoporous pore size of 2.8 nm. The terminal Si-OH on organosilica surface was capped by trimetyl chlorosilane before sulfonylation to benzene groups stretching out of the organosilica surface. Diamines were anchored to organosilica by reaction with sulfonylated benzene groups in organosilica.
Keywords:mesoporous molecular sieve MCM-41 benzene functionalized organic-inorganic hybrid in-situ sulfonylation
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