Bio-Inspired Cu/Pd Bimetallic Catalysts Facilitating One-Pot Relay Catalysis of Homo-Couplings of Arylboronic Acids

IF 3.7 2区 化学 Q2 CHEMISTRY, APPLIED Applied Organometallic Chemistry Pub Date : 2024-08-20 DOI:10.1002/aoc.7688
Jiayi Huang, Zhihao Shan, Yuling Huang, Shuyao Zhang, Ting Lin, Yiqun Li
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Abstract

Inspired by the multienzymatic relay catalysis in nature, herein, we reported a pioneering bio-inspired Cu/Pd bimetallic composite microspheres (Cu/CMC@Pd/C) as a simple and efficient relay catalyst for the homo-coupling of arylboronic acids. In this composite, Pd/C was encapsulated by Cu(II)-crosslinking carboxymethyl cellulose (Cu/CMC). Cu/CMC@Pd/C microspheres were easily achieved by adding a mixture solution of Pd/C and carboxymethyl cellulose into a Cu(II) solution through an ion exchange reaction between carboxylate groups of CMC and Cu(II) ions. The morphology and composition of the as-prepared Cu/CMC@Pd/C microspheres were well characterized using various analytical tools such as FT-IR, XRD, XPS, SEM, TEM, elemental mapping, EDS, and ICP-AES. The analysis indicated that the composite microspheres have a porous structure and Pd/C is uniformly distributed within the interior of the composite microspheres. The porous structure facilitates mass transfer of the substrate and increases the contact area of the catalyst, thus improving reaction efficiency. The performance of Cu/CMC@Pd/C microspheres was assessed in the homo-coupling of arylboronic acid for the synthesis of symmetric biaryl without the need for an aryl halide as a partner. This process mimics a multienzyme catalysis through a relay Cu(I)-catalyzed halogenation of one portion of arylboronic acid and a Pd(0)-catalyzed Suzuki–Miyaura cross-coupling between the in situ generated aryl halide and another portion of arylboronic acid. The results showed that this bio-inspired Cu/CMC@Pd/C has excellent relay catalytic activity with tolerance of broad functional groups, producing the desired symmetrical biaryls in excellent yields within a short reaction time under mild conditions. Moreover, the catalyst can be easily recovered through simple filtration and still has good catalytic activity after six cycles. Consequently, this innovative pseudo-homogeneous Cu/Pd relay catalyst emerges as a convenient and efficient alternative for the synthesis of asymmetric biaryls.

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受生物启发的铜/钯双金属催化剂促进芳硼酸同源偶联反应的一锅继电器催化反应
受自然界多酶中继催化的启发,我们在本文中报道了一种开创性的生物启发铜/钯双金属复合微球(Cu/CMC@Pd/C),作为芳基硼酸均偶联反应的一种简单高效的中继催化剂。在这种复合材料中,Pd/C 被 Cu(II)- 交联羧甲基纤维素(Cu/CMC)包裹。通过 CMC 的羧酸基团与 Cu(II) 离子之间的离子交换反应,将 Pd/C 和羧甲基纤维素的混合溶液加入 Cu(II) 溶液中,很容易就能得到 Cu/CMC@Pd/C 微球。利用 FT-IR、XRD、XPS、SEM、TEM、元素图谱、EDS 和 ICP-AES 等多种分析工具对制备的 Cu/CMC@Pd/C 微球的形态和组成进行了表征。分析表明,复合微球具有多孔结构,Pd/C 均匀地分布在复合微球的内部。多孔结构有利于基质的传质,增加了催化剂的接触面积,从而提高了反应效率。Cu/CMC@Pd/C 微球的性能在芳基硼酸的均偶合合成对称双芳基中得到了评估,无需芳基卤化物作为伴侣。这一过程模拟了多酶催化,通过 Cu(I)中继催化卤化一部分芳硼酸,以及 Pd(0)催化原位生成的芳基卤化物与另一部分芳硼酸之间的 Suzuki-Miyaura 交叉偶联。研究结果表明,这种生物启发的 Cu/CMC@Pd/C 具有优异的中继催化活性,对宽泛的官能团具有耐受性,能在温和的条件下,在较短的反应时间内以优异的产率生成所需的对称双芳基化合物。此外,该催化剂可通过简单过滤轻松回收,并在六个循环后仍具有良好的催化活性。因此,这种创新的假均相铜/钯中继催化剂是合成不对称双芳基化合物的一种便捷、高效的替代方法。
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来源期刊
Applied Organometallic Chemistry
Applied Organometallic Chemistry 化学-无机化学与核化学
CiteScore
7.80
自引率
10.30%
发文量
408
审稿时长
2.2 months
期刊介绍: All new compounds should be satisfactorily identified and proof of their structure given according to generally accepted standards. Structural reports, such as papers exclusively dealing with synthesis and characterization, analytical techniques, or X-ray diffraction studies of metal-organic or organometallic compounds will not be considered. The editors reserve the right to refuse without peer review any manuscript that does not comply with the aims and scope of the journal. Applied Organometallic Chemistry publishes Full Papers, Reviews, Mini Reviews and Communications of scientific research in all areas of organometallic and metal-organic chemistry involving main group metals, transition metals, lanthanides and actinides. All contributions should contain an explicit application of novel compounds, for instance in materials science, nano science, catalysis, chemical vapour deposition, metal-mediated organic synthesis, polymers, bio-organometallics, metallo-therapy, metallo-diagnostics and medicine. Reviews of books covering aspects of the fields of focus are also published.
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Issue Information Issue Information One-Pot Multicomponent Synthesis of Substituted 1,6-Naphthyridine Derivatives Employing 4-Aminocumarin The Role of L-Ligands in Silica-Supported Ti Oxo/Imido Heterometathesis Catalysts Cover Image
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