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Exploring a Route to Cyclic Acenes by On‐Surface Synthesis
A route to generate cyclacenes by on‐surface synthesis is explored. We started by synthesizing two tetraepoxycyclacenes by sequences of Diels–Alder cycloadditions. Subsequently, these molecules were deposited onto Cu(111) and scanning‐tunneling‐microscopy(STM)‐based atom manipulation was employed to...
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Published in: | Angewandte Chemie International Edition 2019-07, Vol.58 (27), p.9038-9042 |
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creator | Schulz, Fabian García, Fátima Kaiser, Katharina Pérez, Dolores Guitián, Enrique Gross, Leo Peña, Diego |
description | A route to generate cyclacenes by on‐surface synthesis is explored. We started by synthesizing two tetraepoxycyclacenes by sequences of Diels–Alder cycloadditions. Subsequently, these molecules were deposited onto Cu(111) and scanning‐tunneling‐microscopy(STM)‐based atom manipulation was employed to dissociate the oxygen atoms. Atomic force microscopy (AFM) with CO‐functionalized tips enabled the detailed characterization of the reaction products and revealed that, at most, two oxygens per molecule could be removed. Importantly, our experimental results suggest that the generation of cyclacenes by the described route might be possible for larger epoxycyclacenes.
Coming full circle: A route to obtain cyclacenes by combining solution and on‐surface chemistry is proposed. Epoxycyclacenes were prepared by a sequence of Diels–Alder cycloadditons, and they were visualized and partially deoxygenated on the Cu(111) surface by scanning probe microscopy. |
doi_str_mv | 10.1002/anie.201902784 |
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Coming full circle: A route to obtain cyclacenes by combining solution and on‐surface chemistry is proposed. Epoxycyclacenes were prepared by a sequence of Diels–Alder cycloadditons, and they were visualized and partially deoxygenated on the Cu(111) surface by scanning probe microscopy.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>ISSN: 1521-3773</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201902784</identifier><identifier>PMID: 31026104</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>arynes ; Atomic force microscopy ; carbon nanobelts ; Communication ; Communications ; cyclacenes ; cycloadditions ; Microscopy ; Oxygen atoms ; Reaction products ; scanning tunneling microscopy ; Synthesis</subject><ispartof>Angewandte Chemie International Edition, 2019-07, Vol.58 (27), p.9038-9042</ispartof><rights>2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.</rights><rights>2019. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5714-2f9af6d45ee836cc8a930ce55f709ac166395b2e3911d24112e32326c2c37e473</citedby><cites>FETCH-LOGICAL-c5714-2f9af6d45ee836cc8a930ce55f709ac166395b2e3911d24112e32326c2c37e473</cites><orcidid>0000-0002-1359-4675 ; 0000-0003-3814-589X ; 0000-0002-7996-283X ; 0000-0003-4785-3812 ; 0000-0003-0877-5938 ; 0000-0001-7519-8005 ; 0000-0002-5337-4159</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31026104$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schulz, Fabian</creatorcontrib><creatorcontrib>García, Fátima</creatorcontrib><creatorcontrib>Kaiser, Katharina</creatorcontrib><creatorcontrib>Pérez, Dolores</creatorcontrib><creatorcontrib>Guitián, Enrique</creatorcontrib><creatorcontrib>Gross, Leo</creatorcontrib><creatorcontrib>Peña, Diego</creatorcontrib><title>Exploring a Route to Cyclic Acenes by On‐Surface Synthesis</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>A route to generate cyclacenes by on‐surface synthesis is explored. We started by synthesizing two tetraepoxycyclacenes by sequences of Diels–Alder cycloadditions. Subsequently, these molecules were deposited onto Cu(111) and scanning‐tunneling‐microscopy(STM)‐based atom manipulation was employed to dissociate the oxygen atoms. Atomic force microscopy (AFM) with CO‐functionalized tips enabled the detailed characterization of the reaction products and revealed that, at most, two oxygens per molecule could be removed. Importantly, our experimental results suggest that the generation of cyclacenes by the described route might be possible for larger epoxycyclacenes.
Coming full circle: A route to obtain cyclacenes by combining solution and on‐surface chemistry is proposed. 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We started by synthesizing two tetraepoxycyclacenes by sequences of Diels–Alder cycloadditions. Subsequently, these molecules were deposited onto Cu(111) and scanning‐tunneling‐microscopy(STM)‐based atom manipulation was employed to dissociate the oxygen atoms. Atomic force microscopy (AFM) with CO‐functionalized tips enabled the detailed characterization of the reaction products and revealed that, at most, two oxygens per molecule could be removed. Importantly, our experimental results suggest that the generation of cyclacenes by the described route might be possible for larger epoxycyclacenes.
Coming full circle: A route to obtain cyclacenes by combining solution and on‐surface chemistry is proposed. Epoxycyclacenes were prepared by a sequence of Diels–Alder cycloadditons, and they were visualized and partially deoxygenated on the Cu(111) surface by scanning probe microscopy.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31026104</pmid><doi>10.1002/anie.201902784</doi><tpages>5</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0002-1359-4675</orcidid><orcidid>https://orcid.org/0000-0003-3814-589X</orcidid><orcidid>https://orcid.org/0000-0002-7996-283X</orcidid><orcidid>https://orcid.org/0000-0003-4785-3812</orcidid><orcidid>https://orcid.org/0000-0003-0877-5938</orcidid><orcidid>https://orcid.org/0000-0001-7519-8005</orcidid><orcidid>https://orcid.org/0000-0002-5337-4159</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | arynes Atomic force microscopy carbon nanobelts Communication Communications cyclacenes cycloadditions Microscopy Oxygen atoms Reaction products scanning tunneling microscopy Synthesis |
title | Exploring a Route to Cyclic Acenes by On‐Surface Synthesis |
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