Synthesis of Nitrogen-Containing Rubicene and Tetrabenzopentacene Derivatives
Carbon‐based materials, such as acenes, fullerenes, and graphene nanoribbons, are viewed as the potential successors to silicon in the next generation of electronics. Although a number of methodologies provide access to these materials’ all‐carbon variants, relatively fewer strategies readily furnis...
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Veröffentlicht in: | Angewandte Chemie International Edition 2016-03, Vol.55 (10), p.3352-3355 |
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creator | Park, Young S. Dibble, David J. Kim, Juhwan Lopez, Robert C. Vargas, Eriberto Gorodetsky, Alon A. |
description | Carbon‐based materials, such as acenes, fullerenes, and graphene nanoribbons, are viewed as the potential successors to silicon in the next generation of electronics. Although a number of methodologies provide access to these materials’ all‐carbon variants, relatively fewer strategies readily furnish their nitrogen‐doped analogues. Herein, we report the rational design, preparation, and characterization of nitrogen‐containing rubicenes and tetrabenzopentacenes, which can be viewed either as acene derivatives or as molecular fragments of fullerenes and graphene nanoribbons. The reported findings may prove valuable for the development of electron transporting organic semiconductors and for the eventual construction of larger carbonaceous systems.
Variants of classic polycyclic aromatic hydrocarbons: Nitrogen‐containing rubicenes and tetrabenzopentacenes were prepared by using a straightforward approach. The reported synthetic method may enable the development of electron‐transporting organic semiconductors and the eventual construction of larger carbonaceous systems. |
doi_str_mv | 10.1002/anie.201510320 |
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Variants of classic polycyclic aromatic hydrocarbons: Nitrogen‐containing rubicenes and tetrabenzopentacenes were prepared by using a straightforward approach. The reported synthetic method may enable the development of electron‐transporting organic semiconductors and the eventual construction of larger carbonaceous systems.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201510320</identifier><identifier>PMID: 26834003</identifier><identifier>CODEN: ACIEAY</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>Carbon ; Construction ; Derivatives ; Design ; Design engineering ; doping ; Electronics ; Electronics industry ; Fragmentation ; Fragments ; Fullerenes ; Graphene ; Nanostructure ; Nitrogen ; nitrogen heterocycles ; organic electronics ; Organic semiconductors ; rubicene ; Semiconductors ; Silicon ; tetrabenzopentacene</subject><ispartof>Angewandte Chemie International Edition, 2016-03, Vol.55 (10), p.3352-3355</ispartof><rights>2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5420-87df09c7b20de11113a0a20d2cbc6fbbef03e82b229b133d63679442364644af3</citedby><cites>FETCH-LOGICAL-c5420-87df09c7b20de11113a0a20d2cbc6fbbef03e82b229b133d63679442364644af3</cites></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.201510320$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.201510320$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26834003$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Young S.</creatorcontrib><creatorcontrib>Dibble, David J.</creatorcontrib><creatorcontrib>Kim, Juhwan</creatorcontrib><creatorcontrib>Lopez, Robert C.</creatorcontrib><creatorcontrib>Vargas, Eriberto</creatorcontrib><creatorcontrib>Gorodetsky, Alon A.</creatorcontrib><title>Synthesis of Nitrogen-Containing Rubicene and Tetrabenzopentacene Derivatives</title><title>Angewandte Chemie International Edition</title><addtitle>Angew. Chem. Int. Ed</addtitle><description>Carbon‐based materials, such as acenes, fullerenes, and graphene nanoribbons, are viewed as the potential successors to silicon in the next generation of electronics. Although a number of methodologies provide access to these materials’ all‐carbon variants, relatively fewer strategies readily furnish their nitrogen‐doped analogues. Herein, we report the rational design, preparation, and characterization of nitrogen‐containing rubicenes and tetrabenzopentacenes, which can be viewed either as acene derivatives or as molecular fragments of fullerenes and graphene nanoribbons. The reported findings may prove valuable for the development of electron transporting organic semiconductors and for the eventual construction of larger carbonaceous systems.
Variants of classic polycyclic aromatic hydrocarbons: Nitrogen‐containing rubicenes and tetrabenzopentacenes were prepared by using a straightforward approach. The reported synthetic method may enable the development of electron‐transporting organic semiconductors and the eventual construction of larger carbonaceous systems.</description><subject>Carbon</subject><subject>Construction</subject><subject>Derivatives</subject><subject>Design</subject><subject>Design engineering</subject><subject>doping</subject><subject>Electronics</subject><subject>Electronics industry</subject><subject>Fragmentation</subject><subject>Fragments</subject><subject>Fullerenes</subject><subject>Graphene</subject><subject>Nanostructure</subject><subject>Nitrogen</subject><subject>nitrogen heterocycles</subject><subject>organic electronics</subject><subject>Organic semiconductors</subject><subject>rubicene</subject><subject>Semiconductors</subject><subject>Silicon</subject><subject>tetrabenzopentacene</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkc9PFDEYhhsiAVy9eiSTePEyy9cf084cyYqIwGp0CYmXpp35Bgq7nbWdQde_nsLihnjQXvqled4nzfcS8obCmAKwA-MdjhnQggJnsEX2aMFozpXiL9IsOM9VWdBd8jLGm8SXJcgdsstkyQUA3yPn31a-v8boYta12dT1obtCn0863xvnnb_Kvg7W1egxM77JZtgHY9H_7paYiMf39xjcnendHcZXZLs184ivn-4RufhwNJt8zM8-H59MDs_yuhAM8lI1LVS1sgwapOlwAybNrLa1bK3FFjiWzDJWWcp5I7lUlRCMSyGFMC0fkXdr7zJ0PwaMvV64WON8bjx2Q9RUybIoKlmphL79C73phuDT7zStQEpQFWP_pJILlFJpXSMyXlN16GIM2OplcAsTVpqCfqhDP9ShN3WkwP6TdrALbDb4n_0noFoDP90cV__R6cPpydFzeb7Outjjr03WhFstFVeFvpweazUT378UcKo_8XsqE6Pm</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Park, Young S.</creator><creator>Dibble, David J.</creator><creator>Kim, Juhwan</creator><creator>Lopez, Robert C.</creator><creator>Vargas, Eriberto</creator><creator>Gorodetsky, Alon A.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20160301</creationdate><title>Synthesis of Nitrogen-Containing Rubicene and Tetrabenzopentacene Derivatives</title><author>Park, Young S. ; Dibble, David J. ; Kim, Juhwan ; Lopez, Robert C. ; Vargas, Eriberto ; Gorodetsky, Alon A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5420-87df09c7b20de11113a0a20d2cbc6fbbef03e82b229b133d63679442364644af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Carbon</topic><topic>Construction</topic><topic>Derivatives</topic><topic>Design</topic><topic>Design engineering</topic><topic>doping</topic><topic>Electronics</topic><topic>Electronics industry</topic><topic>Fragmentation</topic><topic>Fragments</topic><topic>Fullerenes</topic><topic>Graphene</topic><topic>Nanostructure</topic><topic>Nitrogen</topic><topic>nitrogen heterocycles</topic><topic>organic electronics</topic><topic>Organic semiconductors</topic><topic>rubicene</topic><topic>Semiconductors</topic><topic>Silicon</topic><topic>tetrabenzopentacene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Young S.</creatorcontrib><creatorcontrib>Dibble, David J.</creatorcontrib><creatorcontrib>Kim, Juhwan</creatorcontrib><creatorcontrib>Lopez, Robert C.</creatorcontrib><creatorcontrib>Vargas, Eriberto</creatorcontrib><creatorcontrib>Gorodetsky, Alon A.</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Young S.</au><au>Dibble, David J.</au><au>Kim, Juhwan</au><au>Lopez, Robert C.</au><au>Vargas, Eriberto</au><au>Gorodetsky, Alon A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of Nitrogen-Containing Rubicene and Tetrabenzopentacene Derivatives</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew. Chem. Int. Ed</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>55</volume><issue>10</issue><spage>3352</spage><epage>3355</epage><pages>3352-3355</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><coden>ACIEAY</coden><abstract>Carbon‐based materials, such as acenes, fullerenes, and graphene nanoribbons, are viewed as the potential successors to silicon in the next generation of electronics. Although a number of methodologies provide access to these materials’ all‐carbon variants, relatively fewer strategies readily furnish their nitrogen‐doped analogues. Herein, we report the rational design, preparation, and characterization of nitrogen‐containing rubicenes and tetrabenzopentacenes, which can be viewed either as acene derivatives or as molecular fragments of fullerenes and graphene nanoribbons. The reported findings may prove valuable for the development of electron transporting organic semiconductors and for the eventual construction of larger carbonaceous systems.
Variants of classic polycyclic aromatic hydrocarbons: Nitrogen‐containing rubicenes and tetrabenzopentacenes were prepared by using a straightforward approach. The reported synthetic method may enable the development of electron‐transporting organic semiconductors and the eventual construction of larger carbonaceous systems.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>26834003</pmid><doi>10.1002/anie.201510320</doi><tpages>4</tpages><edition>International ed. in English</edition></addata></record> |
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subjects | Carbon Construction Derivatives Design Design engineering doping Electronics Electronics industry Fragmentation Fragments Fullerenes Graphene Nanostructure Nitrogen nitrogen heterocycles organic electronics Organic semiconductors rubicene Semiconductors Silicon tetrabenzopentacene |
title | Synthesis of Nitrogen-Containing Rubicene and Tetrabenzopentacene Derivatives |
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