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钯纳米颗粒与牺牲模板和烧结剂的室温聚结及其在铃木耦合反应中的催化活性。

Room-temperature coalescence of Pd nanoparticles with sacrificial templates and sintering agents, and their catalytic activities in the Suzuki coupling reaction.

作者信息

Okada Soichiro, Nakahara Yoshio, Watanabe Mitsuru, Tamai Toshiyuki, Kobayashi Yasuyuki, Yajima Setsuko

机构信息

Department of Applied Chemistry, Faculty of Systems Engineering, Wakayama University 930 Sakae-dani Wakayama 640-8510 Japan

Morinomiya Center, Osaka Research Institute of Industrial Science and Technology 1-6-50 Morinomiya Joto-ku Osaka 536-8553 Japan.

出版信息

RSC Adv. 2022 May 13;12(23):14535-14543. doi: 10.1039/d2ra00660j. eCollection 2022 May 12.

Abstract

Porous metal structures are very useful for heterogeneous catalysts in organic syntheses. This study reports a novel method to fabricate porous Pd structures by room-temperature (RT) coalescence of Pd nanoparticles (Pd NPs). First, oleylamine-capped Pd NPs were synthesized, and then Pd NP pastes were fabricated by mixing with tri--octylphosphine oxide as a sacrificial template. Finally, the Pd NP paste was dipped into methanol containing a sintering agent. When KOH was used as the sintering agent, porous Pd structures could be successfully obtained at RT. The catalytic activities of porous Pd structures were investigated in the Suzuki coupling reaction and they increased with the increase of the KOH concentration in the sintering process. These results indicate that pre-activation of porous Pd structures by KOH increased the catalytic activities.

摘要

多孔金属结构在有机合成中的多相催化剂方面非常有用。本研究报告了一种通过室温(RT)下钯纳米颗粒(Pd NPs)聚结来制备多孔钯结构的新方法。首先,合成了油胺封端的Pd NPs,然后通过与作为牺牲模板的三辛基氧化膦混合制备了Pd NP糊剂。最后,将Pd NP糊剂浸入含有烧结剂的甲醇中。当使用KOH作为烧结剂时,在室温下可以成功获得多孔钯结构。研究了多孔钯结构在铃木偶联反应中的催化活性,其活性随着烧结过程中KOH浓度的增加而增加。这些结果表明,KOH对多孔钯结构的预活化提高了催化活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82d9/9101230/684d6c6e2761/d2ra00660j-f1.jpg

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