{"title":"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","authors":"Jiayi Huang, Zhihao Shan, Yuling Huang, Shuyao Zhang, Ting Lin, Yiqun Li","doi":"10.1002/aoc.7688","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>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.</p>\n </div>","PeriodicalId":8344,"journal":{"name":"Applied Organometallic Chemistry","volume":"38 12","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2024-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bio-Inspired Cu/Pd Bimetallic Catalysts Facilitating One-Pot Relay Catalysis of Homo-Couplings of Arylboronic Acids\",\"authors\":\"Jiayi Huang, Zhihao Shan, Yuling Huang, Shuyao Zhang, Ting Lin, Yiqun Li\",\"doi\":\"10.1002/aoc.7688\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>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.</p>\\n </div>\",\"PeriodicalId\":8344,\"journal\":{\"name\":\"Applied Organometallic Chemistry\",\"volume\":\"38 12\",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2024-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Organometallic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/aoc.7688\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Organometallic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/aoc.7688","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Bio-Inspired Cu/Pd Bimetallic Catalysts Facilitating One-Pot Relay Catalysis of Homo-Couplings of Arylboronic Acids
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.
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.