The odd-number cyclo[13]carbon and its dimer, cyclo[26]carbon
Molecular rings of carbon atoms (cyclo[ ]carbons, or C ) are excellent benchmarking systems for testing quantum chemical theoretical methods and valuable precursors to other carbon-rich materials. Odd- cyclocarbons, which have been elusive to date, are predicted to be even less stable than even- cyc...
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Veröffentlicht in: | Science (American Association for the Advancement of Science) 2024-05, Vol.384 (6696), p.677-682 |
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creator | Albrecht, Florian Rončević, Igor Gao, Yueze Paschke, Fabian Baiardi, Alberto Tavernelli, Ivano Mishra, Shantanu Anderson, Harry L Gross, Leo |
description | Molecular rings of
carbon atoms (cyclo[
]carbons, or C
) are excellent benchmarking systems for testing quantum chemical theoretical methods and valuable precursors to other carbon-rich materials. Odd-
cyclocarbons, which have been elusive to date, are predicted to be even less stable than even-
cyclocarbons. We report the on-surface synthesis of cyclo[13]carbon, C
, by manipulation of decachlorofluorene with a scanning probe microscope tip. We elucidated the properties of C
by experiment and theoretical modeling. C
adopts an open-shell configuration with a triplet ground state and a kinked geometry, which shows different extents of distortion and carbene localization depending on the molecular environment. Moreover, we prepared and characterized the C
dimer, cyclo[26]carbon, demonstrating the potential of cyclocarbons and their precursors as building blocks for carbon allotropes. |
doi_str_mv | 10.1126/science.ado1399 |
format | Article |
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carbon atoms (cyclo[
]carbons, or C
) are excellent benchmarking systems for testing quantum chemical theoretical methods and valuable precursors to other carbon-rich materials. Odd-
cyclocarbons, which have been elusive to date, are predicted to be even less stable than even-
cyclocarbons. We report the on-surface synthesis of cyclo[13]carbon, C
, by manipulation of decachlorofluorene with a scanning probe microscope tip. We elucidated the properties of C
by experiment and theoretical modeling. C
adopts an open-shell configuration with a triplet ground state and a kinked geometry, which shows different extents of distortion and carbene localization depending on the molecular environment. Moreover, we prepared and characterized the C
dimer, cyclo[26]carbon, demonstrating the potential of cyclocarbons and their precursors as building blocks for carbon allotropes.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.ado1399</identifier><identifier>PMID: 38723091</identifier><language>eng</language><publisher>United States: The American Association for the Advancement of Science</publisher><subject>Carbon ; Carbon cycle ; Chlorine ; Voltage pulses</subject><ispartof>Science (American Association for the Advancement of Science), 2024-05, Vol.384 (6696), p.677-682</ispartof><rights>Copyright © 2024 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c325t-78891c0ea83e8e2d45582b7dcd089ace5cb76f5331f2d51873ce6f7418875bdf3</citedby><cites>FETCH-LOGICAL-c325t-78891c0ea83e8e2d45582b7dcd089ace5cb76f5331f2d51873ce6f7418875bdf3</cites><orcidid>0000-0002-2900-4203 ; 0000-0002-1801-8132 ; 0000-0002-9710-170X ; 0000-0003-2175-8059 ; 0000-0002-1856-7959 ; 0000-0002-5337-4159 ; 0000-0002-7418-9155 ; 0000-0001-5690-1981</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,2885,2886,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38723091$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Albrecht, Florian</creatorcontrib><creatorcontrib>Rončević, Igor</creatorcontrib><creatorcontrib>Gao, Yueze</creatorcontrib><creatorcontrib>Paschke, Fabian</creatorcontrib><creatorcontrib>Baiardi, Alberto</creatorcontrib><creatorcontrib>Tavernelli, Ivano</creatorcontrib><creatorcontrib>Mishra, Shantanu</creatorcontrib><creatorcontrib>Anderson, Harry L</creatorcontrib><creatorcontrib>Gross, Leo</creatorcontrib><title>The odd-number cyclo[13]carbon and its dimer, cyclo[26]carbon</title><title>Science (American Association for the Advancement of Science)</title><addtitle>Science</addtitle><description>Molecular rings of
carbon atoms (cyclo[
]carbons, or C
) are excellent benchmarking systems for testing quantum chemical theoretical methods and valuable precursors to other carbon-rich materials. Odd-
cyclocarbons, which have been elusive to date, are predicted to be even less stable than even-
cyclocarbons. We report the on-surface synthesis of cyclo[13]carbon, C
, by manipulation of decachlorofluorene with a scanning probe microscope tip. We elucidated the properties of C
by experiment and theoretical modeling. C
adopts an open-shell configuration with a triplet ground state and a kinked geometry, which shows different extents of distortion and carbene localization depending on the molecular environment. Moreover, we prepared and characterized the C
dimer, cyclo[26]carbon, demonstrating the potential of cyclocarbons and their precursors as building blocks for carbon allotropes.</description><subject>Carbon</subject><subject>Carbon cycle</subject><subject>Chlorine</subject><subject>Voltage pulses</subject><issn>0036-8075</issn><issn>1095-9203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdkD1PwzAURS0EoqUws6FILAyktf3q2B4YqoovqRJLmRCKHPtFpEriYjdD_z2pGhiY3nDPvXo6hFwzOmWMZ7NoK2wtTo3zDLQ-IWNGtUg1p3BKxpRClioqxYhcxLihtM80nJMRKMmBajYmD-svTLxzads1BYbE7m3tPxh8WhMK3yamdUm1i4mrGgz3Q8yzIb4kZ6WpI14Nd0Lenx7Xy5d09fb8ulysUgtc7FKplGaWolGACrmbC6F4IZ11VGljUdhCZqUAYCV3gikJFrNSzplSUhSuhAm5O-5ug__uMO7ypooW69q06LuYAxWgpe53e_T2H7rxXWj77w4UzwQ9UrMjZYOPMWCZb0PVmLDPGc0PZvPBbD6Y7Rs3w25XNOj--F-V8AOe1XRz</recordid><startdate>20240510</startdate><enddate>20240510</enddate><creator>Albrecht, Florian</creator><creator>Rončević, Igor</creator><creator>Gao, Yueze</creator><creator>Paschke, Fabian</creator><creator>Baiardi, Alberto</creator><creator>Tavernelli, Ivano</creator><creator>Mishra, Shantanu</creator><creator>Anderson, Harry L</creator><creator>Gross, Leo</creator><general>The American Association for the Advancement of Science</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QQ</scope><scope>7QR</scope><scope>7SC</scope><scope>7SE</scope><scope>7SN</scope><scope>7SP</scope><scope>7SR</scope><scope>7SS</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7TK</scope><scope>7TM</scope><scope>7U5</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2900-4203</orcidid><orcidid>https://orcid.org/0000-0002-1801-8132</orcidid><orcidid>https://orcid.org/0000-0002-9710-170X</orcidid><orcidid>https://orcid.org/0000-0003-2175-8059</orcidid><orcidid>https://orcid.org/0000-0002-1856-7959</orcidid><orcidid>https://orcid.org/0000-0002-5337-4159</orcidid><orcidid>https://orcid.org/0000-0002-7418-9155</orcidid><orcidid>https://orcid.org/0000-0001-5690-1981</orcidid></search><sort><creationdate>20240510</creationdate><title>The odd-number cyclo[13]carbon and its dimer, cyclo[26]carbon</title><author>Albrecht, Florian ; 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carbon atoms (cyclo[
]carbons, or C
) are excellent benchmarking systems for testing quantum chemical theoretical methods and valuable precursors to other carbon-rich materials. Odd-
cyclocarbons, which have been elusive to date, are predicted to be even less stable than even-
cyclocarbons. We report the on-surface synthesis of cyclo[13]carbon, C
, by manipulation of decachlorofluorene with a scanning probe microscope tip. We elucidated the properties of C
by experiment and theoretical modeling. C
adopts an open-shell configuration with a triplet ground state and a kinked geometry, which shows different extents of distortion and carbene localization depending on the molecular environment. Moreover, we prepared and characterized the C
dimer, cyclo[26]carbon, demonstrating the potential of cyclocarbons and their precursors as building blocks for carbon allotropes.</abstract><cop>United States</cop><pub>The American Association for the Advancement of Science</pub><pmid>38723091</pmid><doi>10.1126/science.ado1399</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-2900-4203</orcidid><orcidid>https://orcid.org/0000-0002-1801-8132</orcidid><orcidid>https://orcid.org/0000-0002-9710-170X</orcidid><orcidid>https://orcid.org/0000-0003-2175-8059</orcidid><orcidid>https://orcid.org/0000-0002-1856-7959</orcidid><orcidid>https://orcid.org/0000-0002-5337-4159</orcidid><orcidid>https://orcid.org/0000-0002-7418-9155</orcidid><orcidid>https://orcid.org/0000-0001-5690-1981</orcidid></addata></record> |
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issn | 0036-8075 1095-9203 |
language | eng |
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source | Science Magazine |
subjects | Carbon Carbon cycle Chlorine Voltage pulses |
title | The odd-number cyclo[13]carbon and its dimer, cyclo[26]carbon |
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