Selective C−H Bond Cleavage in Methane by Small Gold Clusters
Methane represents the major constituent of natural gas. It is primarily used only as a source of energy by means of combustion, but could also serve as an abundant hydrocarbon feedstock for high quality chemicals. One of the major challenges in catalysis research nowadays is therefore the developme...
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Veröffentlicht in: | Angewandte Chemie (International ed.) 2017-10, Vol.56 (43), p.13406-13410 |
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creator | Lang, Sandra M. Bernhardt, Thorsten M. Chernyy, Valeriy Bakker, Joost M. Barnett, Robert N. Landman, Uzi |
description | Methane represents the major constituent of natural gas. It is primarily used only as a source of energy by means of combustion, but could also serve as an abundant hydrocarbon feedstock for high quality chemicals. One of the major challenges in catalysis research nowadays is therefore the development of materials that selectively cleave one of the four C−H bonds of methane and thus make it amenable for further chemical conversion into valuable compounds. By employing infrared spectroscopy and first‐principles calculations it is uncovered herein that the interaction of methane with small gold cluster cations leads to selective C−H bond dissociation and the formation of hydrido methyl complexes, H‐Aux+‐CH3. The distinctive selectivity offered by these gold clusters originates from a fine interplay between the closed‐shell nature of the d states and relativistic effects in gold. Such fine balance in fundamental interactions could prove to be a tunable feature in the rational design of a catalyst.
Selection by gold: Vibrational spectroscopy in conjunction with first‐principle calculations demonstrate that small gold clusters can mediate the selective dissociation of one of the four C−H bonds of methane, which thus represents the first step towards its conversion into higher‐quality chemicals. The distinct selectivity of these gold clusters originates from their finely balanced electronic structure. Au yellow, C gray, H white. |
doi_str_mv | 10.1002/anie.201706009 |
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Selection by gold: Vibrational spectroscopy in conjunction with first‐principle calculations demonstrate that small gold clusters can mediate the selective dissociation of one of the four C−H bonds of methane, which thus represents the first step towards its conversion into higher‐quality chemicals. The distinct selectivity of these gold clusters originates from their finely balanced electronic structure. Au yellow, C gray, H white.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201706009</identifier><identifier>PMID: 28869784</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>ab initio calculations ; Catalysis ; Cations ; Chemical bonds ; Chemical compounds ; cluster compounds ; Clusters ; C−H bond activation ; Gold ; Hydrogen bonds ; Infrared spectroscopy ; Materials selection ; Methane ; Natural gas ; Relativistic effects ; Selectivity ; vibrational spectroscopy</subject><ispartof>Angewandte Chemie (International ed.), 2017-10, Vol.56 (43), p.13406-13410</ispartof><rights>2017 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4779-571f99f52ddf84fbc45dfd817805e45527421193f140f4db1870c507fdf9ade13</citedby><cites>FETCH-LOGICAL-c4779-571f99f52ddf84fbc45dfd817805e45527421193f140f4db1870c507fdf9ade13</cites><orcidid>0000-0002-1586-1554 ; 0000-0001-7851-0850 ; 0000-0002-1394-7661 ; 0000000213947661 ; 0000000215861554 ; 0000000178510850</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fanie.201706009$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.201706009$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28869784$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1394002$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Lang, Sandra M.</creatorcontrib><creatorcontrib>Bernhardt, Thorsten M.</creatorcontrib><creatorcontrib>Chernyy, Valeriy</creatorcontrib><creatorcontrib>Bakker, Joost M.</creatorcontrib><creatorcontrib>Barnett, Robert N.</creatorcontrib><creatorcontrib>Landman, Uzi</creatorcontrib><title>Selective C−H Bond Cleavage in Methane by Small Gold Clusters</title><title>Angewandte Chemie (International ed.)</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>Methane represents the major constituent of natural gas. It is primarily used only as a source of energy by means of combustion, but could also serve as an abundant hydrocarbon feedstock for high quality chemicals. One of the major challenges in catalysis research nowadays is therefore the development of materials that selectively cleave one of the four C−H bonds of methane and thus make it amenable for further chemical conversion into valuable compounds. By employing infrared spectroscopy and first‐principles calculations it is uncovered herein that the interaction of methane with small gold cluster cations leads to selective C−H bond dissociation and the formation of hydrido methyl complexes, H‐Aux+‐CH3. The distinctive selectivity offered by these gold clusters originates from a fine interplay between the closed‐shell nature of the d states and relativistic effects in gold. Such fine balance in fundamental interactions could prove to be a tunable feature in the rational design of a catalyst.
Selection by gold: Vibrational spectroscopy in conjunction with first‐principle calculations demonstrate that small gold clusters can mediate the selective dissociation of one of the four C−H bonds of methane, which thus represents the first step towards its conversion into higher‐quality chemicals. The distinct selectivity of these gold clusters originates from their finely balanced electronic structure. Au yellow, C gray, H white.</description><subject>ab initio calculations</subject><subject>Catalysis</subject><subject>Cations</subject><subject>Chemical bonds</subject><subject>Chemical compounds</subject><subject>cluster compounds</subject><subject>Clusters</subject><subject>C−H bond activation</subject><subject>Gold</subject><subject>Hydrogen bonds</subject><subject>Infrared spectroscopy</subject><subject>Materials selection</subject><subject>Methane</subject><subject>Natural gas</subject><subject>Relativistic effects</subject><subject>Selectivity</subject><subject>vibrational spectroscopy</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqF0LtOwzAUBmALgaBcVkYUwcKS4pPYtT0hqLhJXAZgtlL7GFK5SYkTUN-AmUfkSXBVKBILkz18_n3OT8gu0D5Qmh0VVYn9jIKgA0rVCukBzyDNhchX453leSokhw2yGcI4einpYJ1sxHOghGQ9cnyPHk1bvmIy_Hz_uExO68omQ4_Fa_GESVklN9g-FxUmo1lyPym8Ty5qPxddaLEJ22TNFT7gzve5RR7Pzx6Gl-n13cXV8OQ6NUwIlXIBTinHM2udZG5kGLfOShCScmScZ4JlACp3wKhjdgRSUMOpcNapwiLkW2R_kVuHttTBlC2aZ1NXVRxeQ65YXC6iwwWaNvVLh6HVkzIY9D7OX3dBxw-4hAwyFunBHzquu6aKK0TFFItz8UFU_YUyTR1Cg05Pm3JSNDMNVM_71_P-9bL_-GDvO7YbTdAu-U_hEagFeCs9zv6J0ye3V2e_4V9aMo7w</recordid><startdate>20171016</startdate><enddate>20171016</enddate><creator>Lang, Sandra M.</creator><creator>Bernhardt, Thorsten M.</creator><creator>Chernyy, Valeriy</creator><creator>Bakker, Joost M.</creator><creator>Barnett, Robert N.</creator><creator>Landman, Uzi</creator><general>Wiley Subscription Services, Inc</general><general>Wiley Blackwell (John Wiley & Sons)</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0002-1586-1554</orcidid><orcidid>https://orcid.org/0000-0001-7851-0850</orcidid><orcidid>https://orcid.org/0000-0002-1394-7661</orcidid><orcidid>https://orcid.org/0000000213947661</orcidid><orcidid>https://orcid.org/0000000215861554</orcidid><orcidid>https://orcid.org/0000000178510850</orcidid></search><sort><creationdate>20171016</creationdate><title>Selective C−H Bond Cleavage in Methane by Small Gold Clusters</title><author>Lang, Sandra M. ; Bernhardt, Thorsten M. ; Chernyy, Valeriy ; Bakker, Joost M. ; Barnett, Robert N. ; Landman, Uzi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4779-571f99f52ddf84fbc45dfd817805e45527421193f140f4db1870c507fdf9ade13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>ab initio calculations</topic><topic>Catalysis</topic><topic>Cations</topic><topic>Chemical bonds</topic><topic>Chemical compounds</topic><topic>cluster compounds</topic><topic>Clusters</topic><topic>C−H bond activation</topic><topic>Gold</topic><topic>Hydrogen bonds</topic><topic>Infrared spectroscopy</topic><topic>Materials selection</topic><topic>Methane</topic><topic>Natural gas</topic><topic>Relativistic effects</topic><topic>Selectivity</topic><topic>vibrational spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lang, Sandra M.</creatorcontrib><creatorcontrib>Bernhardt, Thorsten M.</creatorcontrib><creatorcontrib>Chernyy, Valeriy</creatorcontrib><creatorcontrib>Bakker, Joost M.</creatorcontrib><creatorcontrib>Barnett, Robert N.</creatorcontrib><creatorcontrib>Landman, Uzi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Angewandte Chemie (International ed.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lang, Sandra M.</au><au>Bernhardt, Thorsten M.</au><au>Chernyy, Valeriy</au><au>Bakker, Joost M.</au><au>Barnett, Robert N.</au><au>Landman, Uzi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective C−H Bond Cleavage in Methane by Small Gold Clusters</atitle><jtitle>Angewandte Chemie (International ed.)</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2017-10-16</date><risdate>2017</risdate><volume>56</volume><issue>43</issue><spage>13406</spage><epage>13410</epage><pages>13406-13410</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>Methane represents the major constituent of natural gas. It is primarily used only as a source of energy by means of combustion, but could also serve as an abundant hydrocarbon feedstock for high quality chemicals. One of the major challenges in catalysis research nowadays is therefore the development of materials that selectively cleave one of the four C−H bonds of methane and thus make it amenable for further chemical conversion into valuable compounds. By employing infrared spectroscopy and first‐principles calculations it is uncovered herein that the interaction of methane with small gold cluster cations leads to selective C−H bond dissociation and the formation of hydrido methyl complexes, H‐Aux+‐CH3. The distinctive selectivity offered by these gold clusters originates from a fine interplay between the closed‐shell nature of the d states and relativistic effects in gold. Such fine balance in fundamental interactions could prove to be a tunable feature in the rational design of a catalyst.
Selection by gold: Vibrational spectroscopy in conjunction with first‐principle calculations demonstrate that small gold clusters can mediate the selective dissociation of one of the four C−H bonds of methane, which thus represents the first step towards its conversion into higher‐quality chemicals. The distinct selectivity of these gold clusters originates from their finely balanced electronic structure. Au yellow, C gray, H white.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28869784</pmid><doi>10.1002/anie.201706009</doi><tpages>5</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0002-1586-1554</orcidid><orcidid>https://orcid.org/0000-0001-7851-0850</orcidid><orcidid>https://orcid.org/0000-0002-1394-7661</orcidid><orcidid>https://orcid.org/0000000213947661</orcidid><orcidid>https://orcid.org/0000000215861554</orcidid><orcidid>https://orcid.org/0000000178510850</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | ab initio calculations Catalysis Cations Chemical bonds Chemical compounds cluster compounds Clusters C−H bond activation Gold Hydrogen bonds Infrared spectroscopy Materials selection Methane Natural gas Relativistic effects Selectivity vibrational spectroscopy |
title | Selective C−H Bond Cleavage in Methane by Small Gold Clusters |
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