首页> 外文期刊>ACS Omega >Photo-Assisted Synthesis of a Pd–Ag@CQD Nanohybrid and Its Catalytic Efficiency in Promoting the Suzuki–Miyaura Cross-Coupling Reaction under Ligand-Free and Ambient Conditions
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Photo-Assisted Synthesis of a Pd–Ag@CQD Nanohybrid and Its Catalytic Efficiency in Promoting the Suzuki–Miyaura Cross-Coupling Reaction under Ligand-Free and Ambient Conditions

机译:Pd-Ag @ CQD纳米杂化物的光辅助合成及其在无配体和环境条件下促进铃木-宫浦交叉偶联反应的催化效率

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Supported bimetallic nanoparticles are very promising heterogeneous catalysts for carbon–carbon cross-coupling reactions, though reports focusing on their synergistic activity for promoting such reactions are very limited. In the current study, bimetallic Pd–Ag hybrid nanoparticles supported on carbon quantum dots (CQDs), Pd–Ag@CQDs, were synthesized by a facile and fast UV-light-driven (365 nm) one-pot protocol for the first time to investigate such a synergistic activity. The physico-chemical structural features of the Pd–Ag@CQD nanohybrid were evaluated by UV–vis, Fourier transform infrared, X-ray diffraction, electron-dispersive X-ray, and transmission electron microscopy analyses. The nanohybrid was found to have dimensions in the range of ca. 3–5 nm. The bimetallic Pd–Ag@CQD nanohybrid was utilized as an efficient heterogeneous catalyst for promoting the Suzuki–Miyaura coupling reaction with aryl bromides and aryl chlorides under ligand-free and ambient conditions. The synergistic activity of the components of the nanohybrid induced catalytic enhancement of the cross-coupling reaction in terms of short reaction times ( 90%). The heterogeneous character of the nanohybrid system also enabled easy separation and recyclability (up to six cycles).
机译:负载的双金属纳米颗粒是非常有前途的碳-碳交叉偶联反应的非均相催化剂,尽管有关其促进这种反应的协同活性的报道非常有限。在当前的研究中,首次通过简便且快速的紫外光驱动(365 nm)一锅法合成了碳量子点(CQDs)上负载的双金属Pd-Ag杂化纳米颗粒Pd-Ag @ CQDs。调查这种协同活动。通过紫外可见,傅立叶变换红外,X射线衍射,电子弥散X射线和透射电子显微镜分析评估了Pd-Ag @ CQD纳米杂化物的理化结构特征。发现该纳米杂交体的尺寸在约1μm范围内。 3-5 nm。 Pd-Ag @ CQD双金属纳米杂化物被用作有效的非均相催化剂,用于在无配体和环境条件下促进Suzuki-Miyaura与芳基溴化物和芳基氯化物的偶联反应。就较短的反应时间(90%)而言,纳米杂化物的组分的协同活性诱导了交叉偶联反应的催化增强。纳米杂化系统的异质性还使得其易于分离和回收(最多六个循环)。

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