Highly active, separable and recyclable bipyridine iridium catalysts for C-H borylation reactions
Iridium complexes generated from Ir( i ) precursors and PIB oligomer functionalized bpy ligands efficiently catalyzed the reactions of arenes with bis(pinacolato)diboron under mild conditions to produce a variety of arylboronate compounds. The activity of this PIB bound homogeneous catalyst is simil...
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creator | Mamlouk, Hind Suriboot, Jakkrit Manyam, Praveen Kumar AlYazidi, Ahmed Bergbreiter, David E Madrahimov, Sherzod T |
description | Iridium complexes generated from Ir(
i
) precursors and PIB oligomer functionalized bpy ligands efficiently catalyzed the reactions of arenes with bis(pinacolato)diboron under mild conditions to produce a variety of arylboronate compounds. The activity of this PIB bound homogeneous catalyst is similar to that of an original non-recyclable catalyst which allows it to be used under milder conditions than other reported recyclable catalysts. This oligomer-supported Ir catalyst was successfully recovered through biphasic extraction and reused for eight cycles without a loss of activity. Biphasic separation after the initial use of the catalyst led to an insignificant amount of iridium leaching from the catalyst to the product, and no iridium leaching from the catalyst was observed in the subsequent recycling runs. Arylboronate products obtained after extraction are sufficiently pure as observed by
1
H and
13
C-NMR spectroscopy that they do not require further purification.
Iridium complexes generated from Ir(
i
) precursors and PIB oligomer functionalized bpy ligands efficiently catalyzed the reaction of arenes with bis(pinacolato)diboron under mild conditions to produce a variety of arylboronate compounds. |
doi_str_mv | 10.1039/c7cy01641g |
format | Article |
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i
) precursors and PIB oligomer functionalized bpy ligands efficiently catalyzed the reactions of arenes with bis(pinacolato)diboron under mild conditions to produce a variety of arylboronate compounds. The activity of this PIB bound homogeneous catalyst is similar to that of an original non-recyclable catalyst which allows it to be used under milder conditions than other reported recyclable catalysts. This oligomer-supported Ir catalyst was successfully recovered through biphasic extraction and reused for eight cycles without a loss of activity. Biphasic separation after the initial use of the catalyst led to an insignificant amount of iridium leaching from the catalyst to the product, and no iridium leaching from the catalyst was observed in the subsequent recycling runs. Arylboronate products obtained after extraction are sufficiently pure as observed by
1
H and
13
C-NMR spectroscopy that they do not require further purification.
Iridium complexes generated from Ir(
i
) precursors and PIB oligomer functionalized bpy ligands efficiently catalyzed the reaction of arenes with bis(pinacolato)diboron under mild conditions to produce a variety of arylboronate compounds.</description><identifier>ISSN: 2044-4753</identifier><identifier>EISSN: 2044-4761</identifier><identifier>DOI: 10.1039/c7cy01641g</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Aromatic compounds ; Catalysis ; Catalysts ; Chemical reactions ; Iridium ; Iridium compounds ; Leaching ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance</subject><ispartof>Catalysis science & technology, 2018, Vol.8 (1), p.124-127</ispartof><rights>Copyright Royal Society of Chemistry 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c318t-1e3991ba7633b54462b9a28f915a6323a3b3ad3ac7b232c812d9cb3d2bae4d993</citedby><cites>FETCH-LOGICAL-c318t-1e3991ba7633b54462b9a28f915a6323a3b3ad3ac7b232c812d9cb3d2bae4d993</cites><orcidid>0000-0001-6242-0535 ; 0000-0002-1657-0003 ; 0000-0003-1962-377X ; 0000-0002-3212-3801 ; 0000-0003-1928-3998</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids></links><search><creatorcontrib>Mamlouk, Hind</creatorcontrib><creatorcontrib>Suriboot, Jakkrit</creatorcontrib><creatorcontrib>Manyam, Praveen Kumar</creatorcontrib><creatorcontrib>AlYazidi, Ahmed</creatorcontrib><creatorcontrib>Bergbreiter, David E</creatorcontrib><creatorcontrib>Madrahimov, Sherzod T</creatorcontrib><title>Highly active, separable and recyclable bipyridine iridium catalysts for C-H borylation reactions</title><title>Catalysis science & technology</title><description>Iridium complexes generated from Ir(
i
) precursors and PIB oligomer functionalized bpy ligands efficiently catalyzed the reactions of arenes with bis(pinacolato)diboron under mild conditions to produce a variety of arylboronate compounds. The activity of this PIB bound homogeneous catalyst is similar to that of an original non-recyclable catalyst which allows it to be used under milder conditions than other reported recyclable catalysts. This oligomer-supported Ir catalyst was successfully recovered through biphasic extraction and reused for eight cycles without a loss of activity. Biphasic separation after the initial use of the catalyst led to an insignificant amount of iridium leaching from the catalyst to the product, and no iridium leaching from the catalyst was observed in the subsequent recycling runs. Arylboronate products obtained after extraction are sufficiently pure as observed by
1
H and
13
C-NMR spectroscopy that they do not require further purification.
Iridium complexes generated from Ir(
i
) precursors and PIB oligomer functionalized bpy ligands efficiently catalyzed the reaction of arenes with bis(pinacolato)diboron under mild conditions to produce a variety of arylboronate compounds.</description><subject>Aromatic compounds</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Chemical reactions</subject><subject>Iridium</subject><subject>Iridium compounds</subject><subject>Leaching</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><issn>2044-4753</issn><issn>2044-4761</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpFkM1LxDAQxYMouKx78S4EvInVJJN-5ChFd4UFL3rwVCZpumbptjXpCv3vbXdlncubgd-8YR4h15w9cAbq0aRmYDyRfHNGZoJJGck04eenPoZLsghhy8aSirNMzAiu3OarHiia3v3Yexpshx51bSk2JfXWDKY-jNp1g3elayx1k-531GCP9RD6QKvW0zxaUd36ocbetc24Olm2TbgiFxXWwS7-dE4-Xp7f81W0flu-5k_ryADP-ohbUIprTBMAHUuZCK1QZJXiMSYgAEEDloAm1QKEybgoldFQCo1WlkrBnNwefTvffu9t6Ittu_fNeLIQbHw2lkqIkbo7Usa3IXhbFZ13O_RDwVkxpVjkaf55SHE5wjdH2Adz4v5Thl8X527a</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Mamlouk, Hind</creator><creator>Suriboot, Jakkrit</creator><creator>Manyam, Praveen Kumar</creator><creator>AlYazidi, Ahmed</creator><creator>Bergbreiter, David E</creator><creator>Madrahimov, Sherzod T</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0001-6242-0535</orcidid><orcidid>https://orcid.org/0000-0002-1657-0003</orcidid><orcidid>https://orcid.org/0000-0003-1962-377X</orcidid><orcidid>https://orcid.org/0000-0002-3212-3801</orcidid><orcidid>https://orcid.org/0000-0003-1928-3998</orcidid></search><sort><creationdate>2018</creationdate><title>Highly active, separable and recyclable bipyridine iridium catalysts for C-H borylation reactions</title><author>Mamlouk, Hind ; Suriboot, Jakkrit ; Manyam, Praveen Kumar ; AlYazidi, Ahmed ; Bergbreiter, David E ; Madrahimov, Sherzod T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c318t-1e3991ba7633b54462b9a28f915a6323a3b3ad3ac7b232c812d9cb3d2bae4d993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aromatic compounds</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Chemical reactions</topic><topic>Iridium</topic><topic>Iridium compounds</topic><topic>Leaching</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mamlouk, Hind</creatorcontrib><creatorcontrib>Suriboot, Jakkrit</creatorcontrib><creatorcontrib>Manyam, Praveen Kumar</creatorcontrib><creatorcontrib>AlYazidi, Ahmed</creatorcontrib><creatorcontrib>Bergbreiter, David E</creatorcontrib><creatorcontrib>Madrahimov, Sherzod T</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Catalysis science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mamlouk, Hind</au><au>Suriboot, Jakkrit</au><au>Manyam, Praveen Kumar</au><au>AlYazidi, Ahmed</au><au>Bergbreiter, David E</au><au>Madrahimov, Sherzod T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly active, separable and recyclable bipyridine iridium catalysts for C-H borylation reactions</atitle><jtitle>Catalysis science & technology</jtitle><date>2018</date><risdate>2018</risdate><volume>8</volume><issue>1</issue><spage>124</spage><epage>127</epage><pages>124-127</pages><issn>2044-4753</issn><eissn>2044-4761</eissn><abstract>Iridium complexes generated from Ir(
i
) precursors and PIB oligomer functionalized bpy ligands efficiently catalyzed the reactions of arenes with bis(pinacolato)diboron under mild conditions to produce a variety of arylboronate compounds. The activity of this PIB bound homogeneous catalyst is similar to that of an original non-recyclable catalyst which allows it to be used under milder conditions than other reported recyclable catalysts. This oligomer-supported Ir catalyst was successfully recovered through biphasic extraction and reused for eight cycles without a loss of activity. Biphasic separation after the initial use of the catalyst led to an insignificant amount of iridium leaching from the catalyst to the product, and no iridium leaching from the catalyst was observed in the subsequent recycling runs. Arylboronate products obtained after extraction are sufficiently pure as observed by
1
H and
13
C-NMR spectroscopy that they do not require further purification.
Iridium complexes generated from Ir(
i
) precursors and PIB oligomer functionalized bpy ligands efficiently catalyzed the reaction of arenes with bis(pinacolato)diboron under mild conditions to produce a variety of arylboronate compounds.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c7cy01641g</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0001-6242-0535</orcidid><orcidid>https://orcid.org/0000-0002-1657-0003</orcidid><orcidid>https://orcid.org/0000-0003-1962-377X</orcidid><orcidid>https://orcid.org/0000-0002-3212-3801</orcidid><orcidid>https://orcid.org/0000-0003-1928-3998</orcidid></addata></record> |
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source | Royal Society Of Chemistry Journals 2008- |
subjects | Aromatic compounds Catalysis Catalysts Chemical reactions Iridium Iridium compounds Leaching NMR NMR spectroscopy Nuclear magnetic resonance |
title | Highly active, separable and recyclable bipyridine iridium catalysts for C-H borylation reactions |
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