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Cooperative Bond Activation and Catalytic Reduction of Carbon Dioxide at a Group 13 Metal Center
A single‐component ambiphilic system capable of the cooperative activation of protic, hydridic and apolar HX bonds across a Group 13 metal/activated β‐diketiminato (Nacnac) ligand framework is reported. The hydride complex derived from the activation of H2 is shown to be a competent catalyst for th...
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Published in: | Angewandte Chemie 2015-04, Vol.127 (17), p.5187-5191 |
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container_end_page | 5191 |
container_issue | 17 |
container_start_page | 5187 |
container_title | Angewandte Chemie |
container_volume | 127 |
creator | Abdalla, Joseph A. B. Riddlestone, Ian M. Tirfoin, Rémi Aldridge, Simon |
description | A single‐component ambiphilic system capable of the cooperative activation of protic, hydridic and apolar HX bonds across a Group 13 metal/activated β‐diketiminato (Nacnac) ligand framework is reported. The hydride complex derived from the activation of H2 is shown to be a competent catalyst for the highly selective reduction of CO2 to a methanol derivative. To our knowledge, this process represents the first example of a reduction process of this type catalyzed by a molecular gallium complex.
Ein ambiphiler Gruppe‐13‐Komplex wurde entwickelt, der zur kooperativen Aktivierung protischer, hydridischer und apolarer H‐X‐Bindungen befähigt ist. Der Hydridkomplex, der aus der Aktivierung von H2 entsteht, katalysiert die selektive Umwandlung von CO2 in ein Methanolderivat. Dies ist das erste Beispiel für solch eine durch einen molekularen Ga‐Komplex katalysierte Reduktion. |
doi_str_mv | 10.1002/ange.201500570 |
format | article |
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Ein ambiphiler Gruppe‐13‐Komplex wurde entwickelt, der zur kooperativen Aktivierung protischer, hydridischer und apolarer H‐X‐Bindungen befähigt ist. Der Hydridkomplex, der aus der Aktivierung von H2 entsteht, katalysiert die selektive Umwandlung von CO2 in ein Methanolderivat. Dies ist das erste Beispiel für solch eine durch einen molekularen Ga‐Komplex katalysierte Reduktion.</description><identifier>ISSN: 0044-8249</identifier><identifier>EISSN: 1521-3757</identifier><identifier>DOI: 10.1002/ange.201500570</identifier><language>eng ; ger</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Activation ; Bindungsaktivierung ; Bonding ; Carbon dioxide ; Catalysts ; Chemistry ; Derivatives ; Gallium ; Hydrides ; Kohlendioxid ; Kooperative Reaktivität ; Ligands ; Methyl alcohol ; Reduction ; β-Diketiminat</subject><ispartof>Angewandte Chemie, 2015-04, Vol.127 (17), p.5187-5191</ispartof><rights>2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2330-f09e568250fd62bd27981a9a898401c8aaa5762f201941239ef8d96313db99d93</citedby><cites>FETCH-LOGICAL-c2330-f09e568250fd62bd27981a9a898401c8aaa5762f201941239ef8d96313db99d93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids></links><search><creatorcontrib>Abdalla, Joseph A. B.</creatorcontrib><creatorcontrib>Riddlestone, Ian M.</creatorcontrib><creatorcontrib>Tirfoin, Rémi</creatorcontrib><creatorcontrib>Aldridge, Simon</creatorcontrib><title>Cooperative Bond Activation and Catalytic Reduction of Carbon Dioxide at a Group 13 Metal Center</title><title>Angewandte Chemie</title><addtitle>Angew. Chem</addtitle><description>A single‐component ambiphilic system capable of the cooperative activation of protic, hydridic and apolar HX bonds across a Group 13 metal/activated β‐diketiminato (Nacnac) ligand framework is reported. The hydride complex derived from the activation of H2 is shown to be a competent catalyst for the highly selective reduction of CO2 to a methanol derivative. To our knowledge, this process represents the first example of a reduction process of this type catalyzed by a molecular gallium complex.
Ein ambiphiler Gruppe‐13‐Komplex wurde entwickelt, der zur kooperativen Aktivierung protischer, hydridischer und apolarer H‐X‐Bindungen befähigt ist. Der Hydridkomplex, der aus der Aktivierung von H2 entsteht, katalysiert die selektive Umwandlung von CO2 in ein Methanolderivat. Dies ist das erste Beispiel für solch eine durch einen molekularen Ga‐Komplex katalysierte Reduktion.</description><subject>Activation</subject><subject>Bindungsaktivierung</subject><subject>Bonding</subject><subject>Carbon dioxide</subject><subject>Catalysts</subject><subject>Chemistry</subject><subject>Derivatives</subject><subject>Gallium</subject><subject>Hydrides</subject><subject>Kohlendioxid</subject><subject>Kooperative Reaktivität</subject><subject>Ligands</subject><subject>Methyl alcohol</subject><subject>Reduction</subject><subject>β-Diketiminat</subject><issn>0044-8249</issn><issn>1521-3757</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFkMtP3DAQxi1UJLbAlbOlXrhkmbHz8nEJdGnFS7zFxfUmExQI8dZOKPvf17AIIS6c5qHvN_rmY2wLYYwAYsd0dzQWgAlAksEKG2EiMJJZkn1jI4A4jnIRqzX23ft7AEhFpkbsT2HtnJzpmyfiu7ar-KQMfZhtx00YC9ObdtE3JT-jaihf97YOazcL3V5jn5uKuOm54VNnhzlHyY8oMLygrie3wVZr03rafKvr7PLn_kVxEB2eTH8Vk8OoFFJCVIOiJM1FAnWVilkVzOVolMlVHgOWuTEmyVJRh_9UjEIqqvNKpRJlNVOqUnKdbS_vzp39O5Dv9WPjS2pb05EdvMYMEIREhUH645P03g6uC-40ppkEqRTmQTVeqkpnvXdU67lrHo1baAT9Erh-CVy_Bx4AtQT-NS0tvlDryfF0_yMbLdnG9_T8zhr3oIOjLNHXx1N9uneTnt9e_da38j_VOZFO</recordid><startdate>20150420</startdate><enddate>20150420</enddate><creator>Abdalla, Joseph A. B.</creator><creator>Riddlestone, Ian M.</creator><creator>Tirfoin, Rémi</creator><creator>Aldridge, Simon</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20150420</creationdate><title>Cooperative Bond Activation and Catalytic Reduction of Carbon Dioxide at a Group 13 Metal Center</title><author>Abdalla, Joseph A. B. ; Riddlestone, Ian M. ; Tirfoin, Rémi ; Aldridge, Simon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2330-f09e568250fd62bd27981a9a898401c8aaa5762f201941239ef8d96313db99d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; ger</language><creationdate>2015</creationdate><topic>Activation</topic><topic>Bindungsaktivierung</topic><topic>Bonding</topic><topic>Carbon dioxide</topic><topic>Catalysts</topic><topic>Chemistry</topic><topic>Derivatives</topic><topic>Gallium</topic><topic>Hydrides</topic><topic>Kohlendioxid</topic><topic>Kooperative Reaktivität</topic><topic>Ligands</topic><topic>Methyl alcohol</topic><topic>Reduction</topic><topic>β-Diketiminat</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abdalla, Joseph A. B.</creatorcontrib><creatorcontrib>Riddlestone, Ian M.</creatorcontrib><creatorcontrib>Tirfoin, Rémi</creatorcontrib><creatorcontrib>Aldridge, Simon</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Angewandte Chemie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abdalla, Joseph A. B.</au><au>Riddlestone, Ian M.</au><au>Tirfoin, Rémi</au><au>Aldridge, Simon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cooperative Bond Activation and Catalytic Reduction of Carbon Dioxide at a Group 13 Metal Center</atitle><jtitle>Angewandte Chemie</jtitle><addtitle>Angew. Chem</addtitle><date>2015-04-20</date><risdate>2015</risdate><volume>127</volume><issue>17</issue><spage>5187</spage><epage>5191</epage><pages>5187-5191</pages><issn>0044-8249</issn><eissn>1521-3757</eissn><abstract>A single‐component ambiphilic system capable of the cooperative activation of protic, hydridic and apolar HX bonds across a Group 13 metal/activated β‐diketiminato (Nacnac) ligand framework is reported. The hydride complex derived from the activation of H2 is shown to be a competent catalyst for the highly selective reduction of CO2 to a methanol derivative. To our knowledge, this process represents the first example of a reduction process of this type catalyzed by a molecular gallium complex.
Ein ambiphiler Gruppe‐13‐Komplex wurde entwickelt, der zur kooperativen Aktivierung protischer, hydridischer und apolarer H‐X‐Bindungen befähigt ist. Der Hydridkomplex, der aus der Aktivierung von H2 entsteht, katalysiert die selektive Umwandlung von CO2 in ein Methanolderivat. Dies ist das erste Beispiel für solch eine durch einen molekularen Ga‐Komplex katalysierte Reduktion.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/ange.201500570</doi><tpages>5</tpages></addata></record> |
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language | eng ; ger |
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subjects | Activation Bindungsaktivierung Bonding Carbon dioxide Catalysts Chemistry Derivatives Gallium Hydrides Kohlendioxid Kooperative Reaktivität Ligands Methyl alcohol Reduction β-Diketiminat |
title | Cooperative Bond Activation and Catalytic Reduction of Carbon Dioxide at a Group 13 Metal Center |
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