Piotrowski Piotr, Pawłowska Joanna, Sadło Jarosław Grzegorz, Bilewicz Renata, Kaim Andrzej
Department of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland.
Institute of Nuclear Chemistry and Technology, Dorodna 16, 03-195 Warsaw, Poland.
J Nanopart Res. 2017;19(5):161. doi: 10.1007/s11051-017-3857-z. Epub 2017 Apr 27.
CTEMPO catalytic system linked to a microspherical gold support through a covalent S-Au bond was developed. The CTEMPO@Au composite catalyst had a particle size of 0.5-0.8 μm and was covered with the fullerenes derivative of 2.3 nm diameter bearing ten nitroxyl groups; the organic film showed up to 50 nm thickness. The catalytic composite allowed for the oxidation under mild conditions of various primary and secondary alcohols to the corresponding aldehyde and ketone analogues with efficiencies as high as 79-98%, thus giving values typical for homogeneous catalysis, while retaining at the same time all the advantages of heterogeneous catalysis, e.g., easy separation by filtration from the reaction mixture. The catalytic activity of the resulting system was studied by means of high pressure liquid chromatography. A redox mechanism was proposed for the process. In the catalytic cycle of the oxidation process, the TEMPO moiety was continuously regenerated in situ with an applied primary oxidant, for example, O/Fe system. The new intermediate composite components and the final catalyst were characterized by various spectroscopic methods and thermogravimetry. Graphical abstractᅟ.
开发了一种通过共价 S-Au 键与微球形金载体相连的 CTEMPO 催化体系。CTEMPO@Au 复合催化剂的粒径为 0.5 - 0.8 微米,表面覆盖着直径为 2.3 纳米、带有十个硝酰基的富勒烯衍生物;有机膜厚度达 50 纳米。该催化复合材料能在温和条件下将各种伯醇和仲醇氧化为相应的醛和酮类似物,效率高达 79 - 98%,从而给出了均相催化的典型值,同时保留了多相催化的所有优点,例如可通过过滤从反应混合物中轻松分离。通过高压液相色谱法研究了所得体系的催化活性。提出了该过程的氧化还原机理。在氧化过程的催化循环中,TEMPO 部分通过施加的初级氧化剂(例如 O/Fe 体系)在原位连续再生。通过各种光谱方法和热重分析法对新的中间复合成分和最终催化剂进行了表征。图形摘要ᅟ 。