Green, Efficient and Reusable Bis(imidazolium) Ionic Liquids Promoted Pd-Catalyzed Aqueous Suzuki Reaction for Organic Functional Materials
Glucopyranoside-substituted asymmetric bis(imidazolium) ionic liquids were used to promote environmentally friendly, efficient and reusable Pd-catalyzed Suzuki reaction between arylboronic acids and 2-bromofluorene, 2,7-dibromo-9,9′-dialkylfluorene. Over 30 carbazole-based fluorene core potential or...
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| Veröffentlicht in: | Catalysis letters 2018-09, Vol.148 (9), p.2696-2702 |
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| creator | Zhou, Zhonggao Yuan, Yangyang Xie, Yongrong Li, Mei |
| description | Glucopyranoside-substituted asymmetric bis(imidazolium) ionic liquids were used to promote environmentally friendly, efficient and reusable Pd-catalyzed Suzuki reaction between arylboronic acids and 2-bromofluorene, 2,7-dibromo-9,9′-dialkylfluorene. Over 30 carbazole-based fluorene core potential organic functional materials were synthesized. In addition, recyclability of catalyst system was inspected on the Suzuki reaction observing nearly no loss in catalytic activity up to five cycles.
Graphical Abstract
Development of green, efficient and recycle glucopyranoside substituted bis(imidazolium) ILs promoted Pd-catalyzed aqueous Suzuki reaction for OFMs. |
| doi_str_mv | 10.1007/s10562-018-2452-y |
| format | Article |
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Graphical Abstract
Development of green, efficient and recycle glucopyranoside substituted bis(imidazolium) ILs promoted Pd-catalyzed aqueous Suzuki reaction for OFMs.</description><identifier>ISSN: 1011-372X</identifier><identifier>EISSN: 1572-879X</identifier><identifier>DOI: 10.1007/s10562-018-2452-y</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Carbazoles ; Catalysis ; Catalytic activity ; Chemical reactions ; Chemical synthesis ; Chemistry ; Chemistry and Materials Science ; Functional materials ; Industrial Chemistry/Chemical Engineering ; Ionic liquids ; Ions ; LEDs ; Organometallic Chemistry ; Palladium ; Physical Chemistry ; Recyclability ; Solvents ; Substitutes ; Substitution reactions ; Sustainable development</subject><ispartof>Catalysis letters, 2018-09, Vol.148 (9), p.2696-2702</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>COPYRIGHT 2018 Springer</rights><rights>Catalysis Letters is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-ce7cb8444ddbf31f9ec46ca98b0740ee7857a08457c195124cc6e2a125202f7c3</citedby><cites>FETCH-LOGICAL-c392t-ce7cb8444ddbf31f9ec46ca98b0740ee7857a08457c195124cc6e2a125202f7c3</cites><orcidid>0000-0002-0003-2374</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10562-018-2452-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10562-018-2452-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids></links><search><creatorcontrib>Zhou, Zhonggao</creatorcontrib><creatorcontrib>Yuan, Yangyang</creatorcontrib><creatorcontrib>Xie, Yongrong</creatorcontrib><creatorcontrib>Li, Mei</creatorcontrib><title>Green, Efficient and Reusable Bis(imidazolium) Ionic Liquids Promoted Pd-Catalyzed Aqueous Suzuki Reaction for Organic Functional Materials</title><title>Catalysis letters</title><addtitle>Catal Lett</addtitle><description>Glucopyranoside-substituted asymmetric bis(imidazolium) ionic liquids were used to promote environmentally friendly, efficient and reusable Pd-catalyzed Suzuki reaction between arylboronic acids and 2-bromofluorene, 2,7-dibromo-9,9′-dialkylfluorene. Over 30 carbazole-based fluorene core potential organic functional materials were synthesized. In addition, recyclability of catalyst system was inspected on the Suzuki reaction observing nearly no loss in catalytic activity up to five cycles.
Graphical Abstract
Development of green, efficient and recycle glucopyranoside substituted bis(imidazolium) ILs promoted Pd-catalyzed aqueous Suzuki reaction for OFMs.</description><subject>Carbazoles</subject><subject>Catalysis</subject><subject>Catalytic activity</subject><subject>Chemical reactions</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Functional materials</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Ionic liquids</subject><subject>Ions</subject><subject>LEDs</subject><subject>Organometallic Chemistry</subject><subject>Palladium</subject><subject>Physical Chemistry</subject><subject>Recyclability</subject><subject>Solvents</subject><subject>Substitutes</subject><subject>Substitution reactions</subject><subject>Sustainable development</subject><issn>1011-372X</issn><issn>1572-879X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp1kc1KJDEUhQsZYRz1AWYXcDMDRpN0pZJa9jT-QYuiM-AupFM3TZyqRJPKovsVfGnT1oCrIYubeznf4cCpqu-UnFFCxHmihDcMEyoxqznDm73qgHLBsBTt05fyJ5TimWBPX6tvKT0TQlpB24Pq7SoC-FN0Ya0zDvyItO_QA-SkVz2gXy79cIPr9Db0Lg8_0U3wzqCle82uS-g-hiGM0KH7Di_0qPvNtizz1wwhJ_SYt_mvK2bajC54ZENEd3Gtdw6X2X8cdY9u9QjR6T4dVfu2DDj-Nw-rP5cXvxfXeHl3dbOYL7GZtWzEBoRZybquu25lZ9S2YOrG6FauiKgJgJBcaCJrLgxtOWW1MQ0wTRlnhFlhZofVyeT7EkOJmkb1HHIsUZJirCGUNC0TRXU2qda6B-W8DWPUprwOBmeCB-vKfc45441kUhaAToCJIaUIVr1EN-i4UZSoXUlqKkmVktSuJLUpDJuYVLR-DfEzyv-hdyqUlnk</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Zhou, Zhonggao</creator><creator>Yuan, Yangyang</creator><creator>Xie, Yongrong</creator><creator>Li, Mei</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0002-0003-2374</orcidid></search><sort><creationdate>20180901</creationdate><title>Green, Efficient and Reusable Bis(imidazolium) Ionic Liquids Promoted Pd-Catalyzed Aqueous Suzuki Reaction for Organic Functional Materials</title><author>Zhou, Zhonggao ; 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Over 30 carbazole-based fluorene core potential organic functional materials were synthesized. In addition, recyclability of catalyst system was inspected on the Suzuki reaction observing nearly no loss in catalytic activity up to five cycles.
Graphical Abstract
Development of green, efficient and recycle glucopyranoside substituted bis(imidazolium) ILs promoted Pd-catalyzed aqueous Suzuki reaction for OFMs.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10562-018-2452-y</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0003-2374</orcidid></addata></record> |
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| ispartof | Catalysis letters, 2018-09, Vol.148 (9), p.2696-2702 |
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| subjects | Carbazoles Catalysis Catalytic activity Chemical reactions Chemical synthesis Chemistry Chemistry and Materials Science Functional materials Industrial Chemistry/Chemical Engineering Ionic liquids Ions LEDs Organometallic Chemistry Palladium Physical Chemistry Recyclability Solvents Substitutes Substitution reactions Sustainable development |
| title | Green, Efficient and Reusable Bis(imidazolium) Ionic Liquids Promoted Pd-Catalyzed Aqueous Suzuki Reaction for Organic Functional Materials |
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