配位笼基Ⅱ型孔性液体及其催化1-癸烯加氢性能OACHSSCD
Coordination-cage-based type Ⅱ porous liquids and their catalytic performance in 1-decene hydrogenation
为拓展孔性液体的应用领域,对孔性液体的孔道尺寸与化学性质进行调控,探究其催化性能及在催化反应中的应用.将钒氧-有机分子笼(HD)溶解于聚乙二醇(PEG-2000)中合成了配位笼基Ⅱ型孔性液体(HD/PEG),加入醋酸钯(C4H6O4Pd)后,利用PEG-2000的还原性能在HD/PEG中原位合成钯纳米颗粒.钯纳米颗粒并未占据HD的本征孔,使反应后的液体(HD/Pd/PEG)仍然具有永久孔道结构.HD/Pd/PEG在温和条件(t=40℃、p(H2)=1.01×105 Pa)下反应1 h后,对1-癸烯加氢反应表现出高效催化活性:1-癸烯转化率达99.2%,目标产物癸烷选择性为98.5%,产率为97.7%.HD/Pd/PEG中高度分散的钯纳米颗粒与本征孔结构之间的协同效应,显著提高了 1-癸烯的加氢转化率并加快了反应速率.本研究证实了该类孔性液体在催化领域具有良好应用潜力,为其应用领域的拓展提供了重要支撑.
To expand the application scope of porous liquids,this study explores their catalytic performance and applications in catalytic reactions by controlling pore size and chemical properties.A coordination cage-based type Ⅱ porous liquid(HD/PEG)was synthesized by dissolving a vanadium oxo-organic molecular cage(HD)into polyethylene glycol(PEG-2000).Palladium acetate(C4H6O4Pd)was then added,and palladium nanoparticles were synthesized in situ within HD/PEG via the reducing capability of PEG-2000.The palladium nanoparticles did not occupy the intrinsic pores of HD.Therefore,the resulting liquid(HD/Pd/PEG)retained a permanent porous structure after the reaction.Under mild conditions(t=40 ℃,p(H2)=1.01×105 Pa),the HD/Pd/PEG catalyst exhibited high catalytic activity for the hydrogenation of 1-decene within 1 h,achieving 99.2%conversion,98.5%selectivity toward the target product decane,and a yield of 97.7%.The synergistic effect between the highly dispersed palladium nanoparticles and the intrinsic porous structure in HD/Pd/PEG significantly enhanced both the conversion in the hydrogenation of 1-decene and the reaction rate.This study demonstrates the promising potential of this type of porous liquid in catalysis and provides important support for further expansion of its application scope.
韩雨;张竹修;崔咪芬
南京工业大学化工学院,材料化学工程全国重点实验室,江苏 南京 211800南京工业大学化工学院,材料化学工程全国重点实验室,江苏 南京 211800南京工业大学化工学院,材料化学工程全国重点实验室,江苏 南京 211800
化学化工
孔性液体配位笼金属纳米颗粒催化加氢反应
porous liquidscoordination cagemetal nanoparticlescatalysishydrogenation reaction
《南京工业大学学报(自然科学版)》 2026 (1)
52-59,8
国家重点研发计划(2023YFC3905401)江苏省省级重点研发计划(BE2021710)
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