[19]Starphene: Combined In-Solution and On-Surface Synthesis Towards the Largest Starphene
Starphenes are structurally appealing three-fold symmetric polycyclic aromatic compounds with potential interesting applications in molecular electronics and nanotechnology. This family of star-shaped polyarenes can be regarded as three acenes that are connected through a single benzene ring. In fac...
Gespeichert in:
Veröffentlicht in: | Angewandte Chemie International Edition 2024-11, p.e202411861 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | e202411861 |
container_title | Angewandte Chemie International Edition |
container_volume | |
creator | Besteiro-Sáez, Javier Mateo, Luis M Salaverría, Sergio Wang, Tao Angulo-Portugal, Paula Calupitan, Jan Patrick Rodríguez-Fernández, Jonathan García-Fuente, Amador Ferrer, Jaime Pérez, Dolores Corso, Martina de Oteyza, Dimas G Peña, Diego |
description | Starphenes are structurally appealing three-fold symmetric polycyclic aromatic compounds with potential interesting applications in molecular electronics and nanotechnology. This family of star-shaped polyarenes can be regarded as three acenes that are connected through a single benzene ring. In fact, just like acenes, unsubstituted large starphenes are poorly soluble and highly reactive molecules under ambient conditions making their synthesis difficult to achieve. Herein, we report two different synthetic strategies to obtain a starphene formed by 19 cata-fused benzene rings distributed within three hexacene branches. This molecule, which is the largest starphene that has been obtained to date, was prepared by combining solution-phase and on-surface synthesis. [19]Starphene was characterized by high-resolution scanning tunneling microscopy (STM) and spectroscopy (STS) showing a remarkable small HOMO-LUMO transport gap (0.9 eV). |
doi_str_mv | 10.1002/anie.202411861 |
format | Article |
fullrecord | <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_anie_202411861</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>39110601</sourcerecordid><originalsourceid>FETCH-LOGICAL-c147t-b0d84d494624d1b1e4dae7b6171a3803f3ecda4ef89865b7de309fccf792c0313</originalsourceid><addsrcrecordid>eNo9kM9LwzAcxYMobk6vHiX_QGe-Tdqk3mT4Y1DYYfOiSEmTb1xlTUfSIfvv7Zju9N6D997hQ8gtsCkwlt5r3-A0ZakAUDmckTFkKSRcSn4-eMF5IlUGI3IV4_fQV4rll2TECwCWMxiT9w8oPpe9Dts1enygs66tG4-Wzn2y7Da7vuk81d7SxZB3wWmDdLn3_RpjE-mq-9HBRjpEWurwhbGnp7NrcuH0JuLNn07I2_PTavaalIuX-eyxTAwI2Sc1s0pYUYg8FRZqQGE1yjoHCZorxh1HY7VApwqVZ7W0yFnhjHGySA3jwCdkevw1oYsxoKu2oWl12FfAqgOk6gCpOkEaBnfHwXZXt2hP9X8q_BcWVWMx</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>[19]Starphene: Combined In-Solution and On-Surface Synthesis Towards the Largest Starphene</title><source>Access via Wiley Online Library</source><creator>Besteiro-Sáez, Javier ; Mateo, Luis M ; Salaverría, Sergio ; Wang, Tao ; Angulo-Portugal, Paula ; Calupitan, Jan Patrick ; Rodríguez-Fernández, Jonathan ; García-Fuente, Amador ; Ferrer, Jaime ; Pérez, Dolores ; Corso, Martina ; de Oteyza, Dimas G ; Peña, Diego</creator><creatorcontrib>Besteiro-Sáez, Javier ; Mateo, Luis M ; Salaverría, Sergio ; Wang, Tao ; Angulo-Portugal, Paula ; Calupitan, Jan Patrick ; Rodríguez-Fernández, Jonathan ; García-Fuente, Amador ; Ferrer, Jaime ; Pérez, Dolores ; Corso, Martina ; de Oteyza, Dimas G ; Peña, Diego</creatorcontrib><description>Starphenes are structurally appealing three-fold symmetric polycyclic aromatic compounds with potential interesting applications in molecular electronics and nanotechnology. This family of star-shaped polyarenes can be regarded as three acenes that are connected through a single benzene ring. In fact, just like acenes, unsubstituted large starphenes are poorly soluble and highly reactive molecules under ambient conditions making their synthesis difficult to achieve. Herein, we report two different synthetic strategies to obtain a starphene formed by 19 cata-fused benzene rings distributed within three hexacene branches. This molecule, which is the largest starphene that has been obtained to date, was prepared by combining solution-phase and on-surface synthesis. [19]Starphene was characterized by high-resolution scanning tunneling microscopy (STM) and spectroscopy (STS) showing a remarkable small HOMO-LUMO transport gap (0.9 eV).</description><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.202411861</identifier><identifier>PMID: 39110601</identifier><language>eng</language><publisher>Germany</publisher><ispartof>Angewandte Chemie International Edition, 2024-11, p.e202411861</ispartof><rights>2024 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c147t-b0d84d494624d1b1e4dae7b6171a3803f3ecda4ef89865b7de309fccf792c0313</cites><orcidid>0000-0001-9448-6328 ; 0000-0002-1770-0025 ; 0000-0003-3814-589X ; 0000-0003-0877-5938 ; 0000-0002-8592-1284 ; 0000-0002-6545-5028</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39110601$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Besteiro-Sáez, Javier</creatorcontrib><creatorcontrib>Mateo, Luis M</creatorcontrib><creatorcontrib>Salaverría, Sergio</creatorcontrib><creatorcontrib>Wang, Tao</creatorcontrib><creatorcontrib>Angulo-Portugal, Paula</creatorcontrib><creatorcontrib>Calupitan, Jan Patrick</creatorcontrib><creatorcontrib>Rodríguez-Fernández, Jonathan</creatorcontrib><creatorcontrib>García-Fuente, Amador</creatorcontrib><creatorcontrib>Ferrer, Jaime</creatorcontrib><creatorcontrib>Pérez, Dolores</creatorcontrib><creatorcontrib>Corso, Martina</creatorcontrib><creatorcontrib>de Oteyza, Dimas G</creatorcontrib><creatorcontrib>Peña, Diego</creatorcontrib><title>[19]Starphene: Combined In-Solution and On-Surface Synthesis Towards the Largest Starphene</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>Starphenes are structurally appealing three-fold symmetric polycyclic aromatic compounds with potential interesting applications in molecular electronics and nanotechnology. This family of star-shaped polyarenes can be regarded as three acenes that are connected through a single benzene ring. In fact, just like acenes, unsubstituted large starphenes are poorly soluble and highly reactive molecules under ambient conditions making their synthesis difficult to achieve. Herein, we report two different synthetic strategies to obtain a starphene formed by 19 cata-fused benzene rings distributed within three hexacene branches. This molecule, which is the largest starphene that has been obtained to date, was prepared by combining solution-phase and on-surface synthesis. [19]Starphene was characterized by high-resolution scanning tunneling microscopy (STM) and spectroscopy (STS) showing a remarkable small HOMO-LUMO transport gap (0.9 eV).</description><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kM9LwzAcxYMobk6vHiX_QGe-Tdqk3mT4Y1DYYfOiSEmTb1xlTUfSIfvv7Zju9N6D997hQ8gtsCkwlt5r3-A0ZakAUDmckTFkKSRcSn4-eMF5IlUGI3IV4_fQV4rll2TECwCWMxiT9w8oPpe9Dts1enygs66tG4-Wzn2y7Da7vuk81d7SxZB3wWmDdLn3_RpjE-mq-9HBRjpEWurwhbGnp7NrcuH0JuLNn07I2_PTavaalIuX-eyxTAwI2Sc1s0pYUYg8FRZqQGE1yjoHCZorxh1HY7VApwqVZ7W0yFnhjHGySA3jwCdkevw1oYsxoKu2oWl12FfAqgOk6gCpOkEaBnfHwXZXt2hP9X8q_BcWVWMx</recordid><startdate>20241109</startdate><enddate>20241109</enddate><creator>Besteiro-Sáez, Javier</creator><creator>Mateo, Luis M</creator><creator>Salaverría, Sergio</creator><creator>Wang, Tao</creator><creator>Angulo-Portugal, Paula</creator><creator>Calupitan, Jan Patrick</creator><creator>Rodríguez-Fernández, Jonathan</creator><creator>García-Fuente, Amador</creator><creator>Ferrer, Jaime</creator><creator>Pérez, Dolores</creator><creator>Corso, Martina</creator><creator>de Oteyza, Dimas G</creator><creator>Peña, Diego</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-9448-6328</orcidid><orcidid>https://orcid.org/0000-0002-1770-0025</orcidid><orcidid>https://orcid.org/0000-0003-3814-589X</orcidid><orcidid>https://orcid.org/0000-0003-0877-5938</orcidid><orcidid>https://orcid.org/0000-0002-8592-1284</orcidid><orcidid>https://orcid.org/0000-0002-6545-5028</orcidid></search><sort><creationdate>20241109</creationdate><title>[19]Starphene: Combined In-Solution and On-Surface Synthesis Towards the Largest Starphene</title><author>Besteiro-Sáez, Javier ; Mateo, Luis M ; Salaverría, Sergio ; Wang, Tao ; Angulo-Portugal, Paula ; Calupitan, Jan Patrick ; Rodríguez-Fernández, Jonathan ; García-Fuente, Amador ; Ferrer, Jaime ; Pérez, Dolores ; Corso, Martina ; de Oteyza, Dimas G ; Peña, Diego</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c147t-b0d84d494624d1b1e4dae7b6171a3803f3ecda4ef89865b7de309fccf792c0313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Besteiro-Sáez, Javier</creatorcontrib><creatorcontrib>Mateo, Luis M</creatorcontrib><creatorcontrib>Salaverría, Sergio</creatorcontrib><creatorcontrib>Wang, Tao</creatorcontrib><creatorcontrib>Angulo-Portugal, Paula</creatorcontrib><creatorcontrib>Calupitan, Jan Patrick</creatorcontrib><creatorcontrib>Rodríguez-Fernández, Jonathan</creatorcontrib><creatorcontrib>García-Fuente, Amador</creatorcontrib><creatorcontrib>Ferrer, Jaime</creatorcontrib><creatorcontrib>Pérez, Dolores</creatorcontrib><creatorcontrib>Corso, Martina</creatorcontrib><creatorcontrib>de Oteyza, Dimas G</creatorcontrib><creatorcontrib>Peña, Diego</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Besteiro-Sáez, Javier</au><au>Mateo, Luis M</au><au>Salaverría, Sergio</au><au>Wang, Tao</au><au>Angulo-Portugal, Paula</au><au>Calupitan, Jan Patrick</au><au>Rodríguez-Fernández, Jonathan</au><au>García-Fuente, Amador</au><au>Ferrer, Jaime</au><au>Pérez, Dolores</au><au>Corso, Martina</au><au>de Oteyza, Dimas G</au><au>Peña, Diego</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>[19]Starphene: Combined In-Solution and On-Surface Synthesis Towards the Largest Starphene</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2024-11-09</date><risdate>2024</risdate><spage>e202411861</spage><pages>e202411861-</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>Starphenes are structurally appealing three-fold symmetric polycyclic aromatic compounds with potential interesting applications in molecular electronics and nanotechnology. This family of star-shaped polyarenes can be regarded as three acenes that are connected through a single benzene ring. In fact, just like acenes, unsubstituted large starphenes are poorly soluble and highly reactive molecules under ambient conditions making their synthesis difficult to achieve. Herein, we report two different synthetic strategies to obtain a starphene formed by 19 cata-fused benzene rings distributed within three hexacene branches. This molecule, which is the largest starphene that has been obtained to date, was prepared by combining solution-phase and on-surface synthesis. [19]Starphene was characterized by high-resolution scanning tunneling microscopy (STM) and spectroscopy (STS) showing a remarkable small HOMO-LUMO transport gap (0.9 eV).</abstract><cop>Germany</cop><pmid>39110601</pmid><doi>10.1002/anie.202411861</doi><orcidid>https://orcid.org/0000-0001-9448-6328</orcidid><orcidid>https://orcid.org/0000-0002-1770-0025</orcidid><orcidid>https://orcid.org/0000-0003-3814-589X</orcidid><orcidid>https://orcid.org/0000-0003-0877-5938</orcidid><orcidid>https://orcid.org/0000-0002-8592-1284</orcidid><orcidid>https://orcid.org/0000-0002-6545-5028</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1433-7851 |
ispartof | Angewandte Chemie International Edition, 2024-11, p.e202411861 |
issn | 1433-7851 1521-3773 |
language | eng |
recordid | cdi_crossref_primary_10_1002_anie_202411861 |
source | Access via Wiley Online Library |
title | [19]Starphene: Combined In-Solution and On-Surface Synthesis Towards the Largest Starphene |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T09%3A24%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=%5B19%5DStarphene:%20Combined%20In-Solution%20and%20On-Surface%20Synthesis%20Towards%20the%20Largest%20Starphene&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Besteiro-S%C3%A1ez,%20Javier&rft.date=2024-11-09&rft.spage=e202411861&rft.pages=e202411861-&rft.issn=1433-7851&rft.eissn=1521-3773&rft_id=info:doi/10.1002/anie.202411861&rft_dat=%3Cpubmed_cross%3E39110601%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/39110601&rfr_iscdi=true |