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首页> 外文期刊>Catalysis Letters >One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina
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One-Pot Myrtenol Amination over Au, Au-Pd and Pd Nanoparticles Supported on Alumina

机译:OU,AU-Pd和PD纳米粒子上的一壶肌腱胺化氧化铝

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One-pot bio-based myrtenol amination was studied in the presence of alumina supported Au, Au-Pd and Pd nanoparticles subjected to the thermal treatment under oxidizing or reducing atmosphere. Myrtenol amination with aniline was carried out under nitrogen atmosphere (9 bar) at 453 K using toluene as a solvent. The effect of the active metal along with the influence of redox pre-treatment on the catalytic behavior in the hydrogen borrowing reaction was explored. The catalyst characterization was done by transmission electron microscopy, X-ray photoelectron spectroscopy, inductively coupled plasma optical emission spectroscopy, nitrogen adsorption. The active metal and the catalysts redox pretreatment affected more noticeably selectivity to the reaction products rather than myrtenol conversion. Monometallic Au/Al2O3 catalyst promoted predominantly formation of the target secondary amine and the corresponding imine without a significant impact of the side reaction of C=C bond hydrogenation in myrtenol, whereas monometallic Pd catalyst activated C=C bond resulting in its hydrogenation. At the same time in the presence of Au-Pd simultaneous hydrogenation of both C=C and C=N bond occurred. Au-Pd catalysts activated in oxygen and hydrogen showed different catalytic activity determined by the composition of surface active sites. Monometallic gold catalyst was more effective in the hydrogen transfer in the case of substrates with competitive unsaturated functional groups.
机译:在氧化铝负载的Au,AU-Pd和Pd纳米粒子的存在下研究了在氧化或减少气氛下进行热处理的氧化铝的Au,Au-Pd和Pd纳米颗粒的存在。使用甲苯作为溶剂,在453 k下在氮气氛(9巴)下进行Myrtenol胺化。探讨了活性金属与氧化还原预处理对氢借用反应中催化行为的影响的影响。催化剂表征通过透射电子显微镜,X射线光电子能谱,电感耦合等离子体光发射光谱,氮吸附来完成。活性金属和催化剂氧化还原预处理对反应产物的影响更为明显,而不是Myrtenol转化。单金属Au / Al2O3催化剂促进靶仲胺和相应的亚胺的主要形成,而没有C = C键氢化在myRTenol中的副反应的显着影响,而单金属Pd催化剂活化的C = C键导致其氢化。同时在存在Au-Pd同时氢化C = C和C = N键的情况下发生。在氧气和氢中活化的AU-Pd催化剂显示出通过表面活性位点的组成测定的不同催化活性。在具有竞争性不饱和官能团的基材的情况下,单金属金催化剂在氢转移中更有效。

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