A magnetically separable palladium catalyst containing a bulky N-heterocyclic carbene ligand for the Suzuki–Miyaura reaction
This work describes the preparation and characterization of a magnetic palladium catalyst with bulky N-heterocyclic carbene (NHC) ligands for the Suzuki-Miyaura cross-coupling reaction. After the 1-(2,6-diisopropylphenyl)-1H-imidazole (1-arylimidazole) was modified on the surface of magnetic polymer...
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Veröffentlicht in: | Green chemistry : an international journal and green chemistry resource : GC 2015-01, Vol.17 (1), p.413-420 |
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description | This work describes the preparation and characterization of a magnetic palladium catalyst with bulky N-heterocyclic carbene (NHC) ligands for the Suzuki-Miyaura cross-coupling reaction. After the 1-(2,6-diisopropylphenyl)-1H-imidazole (1-arylimidazole) was modified on the surface of magnetic polymer carriers, palladium diacetate was employed to synthesize the Pd-NHC complex, affording a palladium loading of 0.23 mmol g super(-1). This magnetic catalyst showed high catalytic activity towards the Suzuki-Miyaura reaction of phenylboronic acids with aryl bromides in the ethanol-water solution (TON > 87 000). After 21 cycling runs, its catalytic activity decreased slightly, and no leaking of palladium was found either in products or in reaction residue. When other sources of palladium (PdCl sub(2) and 3-Cl-pyridinyl) were employed to synthesize the palladium complex, the stability of the magnetic catalyst was greatly improved to perform the catalysis of Suzuki-Miyaura reactions with aryl chlorides at 100 degree C. |
doi_str_mv | 10.1039/c4gc00574k |
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After the 1-(2,6-diisopropylphenyl)-1H-imidazole (1-arylimidazole) was modified on the surface of magnetic polymer carriers, palladium diacetate was employed to synthesize the Pd-NHC complex, affording a palladium loading of 0.23 mmol g super(-1). This magnetic catalyst showed high catalytic activity towards the Suzuki-Miyaura reaction of phenylboronic acids with aryl bromides in the ethanol-water solution (TON > 87 000). After 21 cycling runs, its catalytic activity decreased slightly, and no leaking of palladium was found either in products or in reaction residue. When other sources of palladium (PdCl sub(2) and 3-Cl-pyridinyl) were employed to synthesize the palladium complex, the stability of the magnetic catalyst was greatly improved to perform the catalysis of Suzuki-Miyaura reactions with aryl chlorides at 100 degree C.</description><identifier>ISSN: 1463-9262</identifier><identifier>EISSN: 1463-9270</identifier><identifier>DOI: 10.1039/c4gc00574k</identifier><language>eng</language><subject>Aromatic compounds ; Carbenes ; Catalysts ; Catalytic activity ; Chemical reactions ; Ligands ; Palladium ; Surface chemistry</subject><ispartof>Green chemistry : an international journal and green chemistry resource : GC, 2015-01, Vol.17 (1), p.413-420</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-567ed3d7e39b0c085e3dd4f8505ad4146944e15a42f7385d91df4a0d83e80c473</citedby><cites>FETCH-LOGICAL-c400t-567ed3d7e39b0c085e3dd4f8505ad4146944e15a42f7385d91df4a0d83e80c473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Wang, Z</creatorcontrib><creatorcontrib>Yu, Y</creatorcontrib><creatorcontrib>Zhang, Y X</creatorcontrib><creatorcontrib>Li, S Z</creatorcontrib><creatorcontrib>Qian, H</creatorcontrib><creatorcontrib>Lin, Z Y</creatorcontrib><title>A magnetically separable palladium catalyst containing a bulky N-heterocyclic carbene ligand for the Suzuki–Miyaura reaction</title><title>Green chemistry : an international journal and green chemistry resource : GC</title><description>This work describes the preparation and characterization of a magnetic palladium catalyst with bulky N-heterocyclic carbene (NHC) ligands for the Suzuki-Miyaura cross-coupling reaction. After the 1-(2,6-diisopropylphenyl)-1H-imidazole (1-arylimidazole) was modified on the surface of magnetic polymer carriers, palladium diacetate was employed to synthesize the Pd-NHC complex, affording a palladium loading of 0.23 mmol g super(-1). This magnetic catalyst showed high catalytic activity towards the Suzuki-Miyaura reaction of phenylboronic acids with aryl bromides in the ethanol-water solution (TON > 87 000). After 21 cycling runs, its catalytic activity decreased slightly, and no leaking of palladium was found either in products or in reaction residue. When other sources of palladium (PdCl sub(2) and 3-Cl-pyridinyl) were employed to synthesize the palladium complex, the stability of the magnetic catalyst was greatly improved to perform the catalysis of Suzuki-Miyaura reactions with aryl chlorides at 100 degree C.</description><subject>Aromatic compounds</subject><subject>Carbenes</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Chemical reactions</subject><subject>Ligands</subject><subject>Palladium</subject><subject>Surface chemistry</subject><issn>1463-9262</issn><issn>1463-9270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkbtOxDAURCMEEs-GL3CJkALXsR0nJVrBgngVQB3dtW8Ws9lksZ0iFIh_4A_5EsJDtFQzIx2NNJok2edwxEGUx0bODYDScrGWbHGZi7TMNKz_-TzbTLZDeALgXOdyK3k9YUuctxSdwaYZWKAVepw1xFZjRuv6JTMYsRlCZKZrI7rWtXOGbNY3i4HdpI8UyXdmMI0zI-pn1BJr3Bxby-rOs_hI7K5_6Rfu4-392g3Ye2Se0ETXtbvJRo1NoL1f3Ukezk7vJ-fp1e30YnJylRoJEFOVa7LCahLlDAwUioS1si4UKLRy3FZKSVyhzGotCmVLbmuJYAtBBRipxU5y8NO78t1zTyFWSxcMjQtb6vpQ8QJAipyr8n9UZxnXXBUwooc_qPFdCJ7qauXdEv1Qcai-_qgmcjr5_uNSfAL9qX_x</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Wang, Z</creator><creator>Yu, Y</creator><creator>Zhang, Y X</creator><creator>Li, S Z</creator><creator>Qian, H</creator><creator>Lin, Z Y</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7U6</scope><scope>C1K</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20150101</creationdate><title>A magnetically separable palladium catalyst containing a bulky N-heterocyclic carbene ligand for the Suzuki–Miyaura reaction</title><author>Wang, Z ; Yu, Y ; Zhang, Y X ; Li, S Z ; Qian, H ; Lin, Z Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-567ed3d7e39b0c085e3dd4f8505ad4146944e15a42f7385d91df4a0d83e80c473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aromatic compounds</topic><topic>Carbenes</topic><topic>Catalysts</topic><topic>Catalytic activity</topic><topic>Chemical reactions</topic><topic>Ligands</topic><topic>Palladium</topic><topic>Surface chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Z</creatorcontrib><creatorcontrib>Yu, Y</creatorcontrib><creatorcontrib>Zhang, Y X</creatorcontrib><creatorcontrib>Li, S Z</creatorcontrib><creatorcontrib>Qian, H</creatorcontrib><creatorcontrib>Lin, Z Y</creatorcontrib><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Z</au><au>Yu, Y</au><au>Zhang, Y X</au><au>Li, S Z</au><au>Qian, H</au><au>Lin, Z Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A magnetically separable palladium catalyst containing a bulky N-heterocyclic carbene ligand for the Suzuki–Miyaura reaction</atitle><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle><date>2015-01-01</date><risdate>2015</risdate><volume>17</volume><issue>1</issue><spage>413</spage><epage>420</epage><pages>413-420</pages><issn>1463-9262</issn><eissn>1463-9270</eissn><abstract>This work describes the preparation and characterization of a magnetic palladium catalyst with bulky N-heterocyclic carbene (NHC) ligands for the Suzuki-Miyaura cross-coupling reaction. After the 1-(2,6-diisopropylphenyl)-1H-imidazole (1-arylimidazole) was modified on the surface of magnetic polymer carriers, palladium diacetate was employed to synthesize the Pd-NHC complex, affording a palladium loading of 0.23 mmol g super(-1). This magnetic catalyst showed high catalytic activity towards the Suzuki-Miyaura reaction of phenylboronic acids with aryl bromides in the ethanol-water solution (TON > 87 000). After 21 cycling runs, its catalytic activity decreased slightly, and no leaking of palladium was found either in products or in reaction residue. When other sources of palladium (PdCl sub(2) and 3-Cl-pyridinyl) were employed to synthesize the palladium complex, the stability of the magnetic catalyst was greatly improved to perform the catalysis of Suzuki-Miyaura reactions with aryl chlorides at 100 degree C.</abstract><doi>10.1039/c4gc00574k</doi><tpages>8</tpages></addata></record> |
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subjects | Aromatic compounds Carbenes Catalysts Catalytic activity Chemical reactions Ligands Palladium Surface chemistry |
title | A magnetically separable palladium catalyst containing a bulky N-heterocyclic carbene ligand for the Suzuki–Miyaura reaction |
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