[4 + 2] Cycloaddition Reaction To Approach Diazatwistpentacenes: Synthesis, Structures, Physical Properties, and Self-assembly

Three novel diazatwistpentacenes (1,4,6,13-tetraphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (1, IUPAC name: 9,11,14,16-tetraphenyl-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine); 1,4-di(pyridin-2-yl)-6,13-diphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (2, IUPAC name: 9,16-diphenyl-1...

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Veröffentlicht in:Journal of organic chemistry 2014-05, Vol.79 (10), p.4438-4445
Hauptverfasser: Li, Junbo, Li, Peizhou, Wu, Jiansheng, Gao, Junkuo, Xiong, Wei-Wei, Zhang, Guodong, Zhao, Yanli, Zhang, Qichun
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container_issue 10
container_start_page 4438
container_title Journal of organic chemistry
container_volume 79
creator Li, Junbo
Li, Peizhou
Wu, Jiansheng
Gao, Junkuo
Xiong, Wei-Wei
Zhang, Guodong
Zhao, Yanli
Zhang, Qichun
description Three novel diazatwistpentacenes (1,4,6,13-tetraphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (1, IUPAC name: 9,11,14,16-tetraphenyl-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine); 1,4-di(pyridin-2-yl)-6,13-diphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (2, IUPAC name: 9,16-diphenyl-11,14-di(pyridin-2-yl)-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine); and 1,4-di(thien-2-yl)-6,13-diphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (3, IUPAC name: 9,16-diphenyl-11,14-di(thien-2-yl)-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine)) have been successfully synthesized through [4 + 2] cycloaddition reaction involving in situ arynes as dienophiles and substituted 1,2,4,5-tetrazines as dienes. Their structures have been determined by single-crystal X-ray diffraction, confirming that all compounds have twisted configurations with torsion angles between the pyrene unit and the 2,3-diazaanthrance part as high as 21.52° (for 1), 24.74° (for 2), and 21.14° (for 3). The optical bandgaps for all compounds corroborate the values derived from CV. The calculation done by DFT shows that the HOMO–LUMO bandgaps are in good agreement with experimental data. Interestingly, the substituted groups (phenyl, pyridyl, thienyl) in the 1,4-positions did affect their self-assembly and the optical properties of as-resulted nanostructures. Under the same conditions, compounds 1–3 could self-assemble into different morphologies such as microrods (for 1), nanoprisms (for 2), and nanobelts (for 3). Moreover, the UV–vis absorption and emission spectra of as-prepared nanostructures were largely red-shifted, indicating J-type aggregation for all materials. Surprisingly, both 1 and 2 showed aggregation-induced emission (AIE) effect, while compound 3 showed aggregation-caused quenching (ACQ) effect. Our method to approach novel twisted azaacenes through [4 + 2] reaction could offer a new tool to develop unusual twisted conjugated materials for future optoelectronic applications.
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Their structures have been determined by single-crystal X-ray diffraction, confirming that all compounds have twisted configurations with torsion angles between the pyrene unit and the 2,3-diazaanthrance part as high as 21.52° (for 1), 24.74° (for 2), and 21.14° (for 3). The optical bandgaps for all compounds corroborate the values derived from CV. The calculation done by DFT shows that the HOMO–LUMO bandgaps are in good agreement with experimental data. Interestingly, the substituted groups (phenyl, pyridyl, thienyl) in the 1,4-positions did affect their self-assembly and the optical properties of as-resulted nanostructures. Under the same conditions, compounds 1–3 could self-assemble into different morphologies such as microrods (for 1), nanoprisms (for 2), and nanobelts (for 3). Moreover, the UV–vis absorption and emission spectra of as-prepared nanostructures were largely red-shifted, indicating J-type aggregation for all materials. Surprisingly, both 1 and 2 showed aggregation-induced emission (AIE) effect, while compound 3 showed aggregation-caused quenching (ACQ) effect. Our method to approach novel twisted azaacenes through [4 + 2] reaction could offer a new tool to develop unusual twisted conjugated materials for future optoelectronic applications.</description><identifier>ISSN: 0022-3263</identifier><identifier>EISSN: 1520-6904</identifier><identifier>DOI: 10.1021/jo500400d</identifier><identifier>PMID: 24741990</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Journal of organic chemistry, 2014-05, Vol.79 (10), p.4438-4445</ispartof><rights>Copyright © 2014 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a381t-1c4cc8308df864c103a6fc5e2d6b861d4bd32f06f1095eb4207dc21d89f848c73</citedby><cites>FETCH-LOGICAL-a381t-1c4cc8308df864c103a6fc5e2d6b861d4bd32f06f1095eb4207dc21d89f848c73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jo500400d$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jo500400d$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24741990$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Junbo</creatorcontrib><creatorcontrib>Li, Peizhou</creatorcontrib><creatorcontrib>Wu, Jiansheng</creatorcontrib><creatorcontrib>Gao, Junkuo</creatorcontrib><creatorcontrib>Xiong, Wei-Wei</creatorcontrib><creatorcontrib>Zhang, Guodong</creatorcontrib><creatorcontrib>Zhao, Yanli</creatorcontrib><creatorcontrib>Zhang, Qichun</creatorcontrib><title>[4 + 2] Cycloaddition Reaction To Approach Diazatwistpentacenes: Synthesis, Structures, Physical Properties, and Self-assembly</title><title>Journal of organic chemistry</title><addtitle>J. Org. Chem</addtitle><description>Three novel diazatwistpentacenes (1,4,6,13-tetraphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (1, IUPAC name: 9,11,14,16-tetraphenyl-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine); 1,4-di(pyridin-2-yl)-6,13-diphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (2, IUPAC name: 9,16-diphenyl-11,14-di(pyridin-2-yl)-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine); and 1,4-di(thien-2-yl)-6,13-diphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (3, IUPAC name: 9,16-diphenyl-11,14-di(thien-2-yl)-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine)) have been successfully synthesized through [4 + 2] cycloaddition reaction involving in situ arynes as dienophiles and substituted 1,2,4,5-tetrazines as dienes. Their structures have been determined by single-crystal X-ray diffraction, confirming that all compounds have twisted configurations with torsion angles between the pyrene unit and the 2,3-diazaanthrance part as high as 21.52° (for 1), 24.74° (for 2), and 21.14° (for 3). The optical bandgaps for all compounds corroborate the values derived from CV. The calculation done by DFT shows that the HOMO–LUMO bandgaps are in good agreement with experimental data. Interestingly, the substituted groups (phenyl, pyridyl, thienyl) in the 1,4-positions did affect their self-assembly and the optical properties of as-resulted nanostructures. Under the same conditions, compounds 1–3 could self-assemble into different morphologies such as microrods (for 1), nanoprisms (for 2), and nanobelts (for 3). Moreover, the UV–vis absorption and emission spectra of as-prepared nanostructures were largely red-shifted, indicating J-type aggregation for all materials. Surprisingly, both 1 and 2 showed aggregation-induced emission (AIE) effect, while compound 3 showed aggregation-caused quenching (ACQ) effect. Our method to approach novel twisted azaacenes through [4 + 2] reaction could offer a new tool to develop unusual twisted conjugated materials for future optoelectronic applications.</description><issn>0022-3263</issn><issn>1520-6904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNptkEtLw0AUhQdRbK0u_AMyGxei0TuTSTpxV-oTChZbVyJlMg86kiZhZoLEhb_d1GpX3s09XL57OByEjglcEqDk6r1KABiA2kF9klCI0gzYLuoDUBrFNI176MD7d-gmSZJ91KNsyEiWQR99vTJ8jukbHreyqIRSNtiqxM9ayB8xr_Corl0l5BLfWPEpwof1odZlEFKX2l_jWVuGpfbWX-BZcI0MjdOdni5bb6Uo8NRVtXbBro-iVHimCxMJ7_UqL9pDtGdE4fXR7x6gl7vb-fghmjzdP45Hk0jEnISISCYlj4Erw1MmCcQiNTLRVKU5T4liuYqpgdQQyBKdMwpDJSlRPDOccTmMB-hs4ytd5b3TZlE7uxKuXRBYrDtcbDvs2JMNWzf5Sqst-VdaB5xuACF999e4sov-j9E3L4d5Tg</recordid><startdate>20140516</startdate><enddate>20140516</enddate><creator>Li, Junbo</creator><creator>Li, Peizhou</creator><creator>Wu, Jiansheng</creator><creator>Gao, Junkuo</creator><creator>Xiong, Wei-Wei</creator><creator>Zhang, Guodong</creator><creator>Zhao, Yanli</creator><creator>Zhang, Qichun</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20140516</creationdate><title>[4 + 2] Cycloaddition Reaction To Approach Diazatwistpentacenes: Synthesis, Structures, Physical Properties, and Self-assembly</title><author>Li, Junbo ; Li, Peizhou ; Wu, Jiansheng ; Gao, Junkuo ; Xiong, Wei-Wei ; Zhang, Guodong ; Zhao, Yanli ; Zhang, Qichun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a381t-1c4cc8308df864c103a6fc5e2d6b861d4bd32f06f1095eb4207dc21d89f848c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Junbo</creatorcontrib><creatorcontrib>Li, Peizhou</creatorcontrib><creatorcontrib>Wu, Jiansheng</creatorcontrib><creatorcontrib>Gao, Junkuo</creatorcontrib><creatorcontrib>Xiong, Wei-Wei</creatorcontrib><creatorcontrib>Zhang, Guodong</creatorcontrib><creatorcontrib>Zhao, Yanli</creatorcontrib><creatorcontrib>Zhang, Qichun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Junbo</au><au>Li, Peizhou</au><au>Wu, Jiansheng</au><au>Gao, Junkuo</au><au>Xiong, Wei-Wei</au><au>Zhang, Guodong</au><au>Zhao, Yanli</au><au>Zhang, Qichun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>[4 + 2] Cycloaddition Reaction To Approach Diazatwistpentacenes: Synthesis, Structures, Physical Properties, and Self-assembly</atitle><jtitle>Journal of organic chemistry</jtitle><addtitle>J. Org. Chem</addtitle><date>2014-05-16</date><risdate>2014</risdate><volume>79</volume><issue>10</issue><spage>4438</spage><epage>4445</epage><pages>4438-4445</pages><issn>0022-3263</issn><eissn>1520-6904</eissn><abstract>Three novel diazatwistpentacenes (1,4,6,13-tetraphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (1, IUPAC name: 9,11,14,16-tetraphenyl-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine); 1,4-di(pyridin-2-yl)-6,13-diphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (2, IUPAC name: 9,16-diphenyl-11,14-di(pyridin-2-yl)-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine); and 1,4-di(thien-2-yl)-6,13-diphenyl-7:8,11:12-bisbenzo-2,3-diazatwistpentacene (3, IUPAC name: 9,16-diphenyl-11,14-di(thien-2-yl)-1,6-dihydrobenzo[8,9]triphenyleno[2,3-g]phthalazine)) have been successfully synthesized through [4 + 2] cycloaddition reaction involving in situ arynes as dienophiles and substituted 1,2,4,5-tetrazines as dienes. Their structures have been determined by single-crystal X-ray diffraction, confirming that all compounds have twisted configurations with torsion angles between the pyrene unit and the 2,3-diazaanthrance part as high as 21.52° (for 1), 24.74° (for 2), and 21.14° (for 3). The optical bandgaps for all compounds corroborate the values derived from CV. The calculation done by DFT shows that the HOMO–LUMO bandgaps are in good agreement with experimental data. Interestingly, the substituted groups (phenyl, pyridyl, thienyl) in the 1,4-positions did affect their self-assembly and the optical properties of as-resulted nanostructures. Under the same conditions, compounds 1–3 could self-assemble into different morphologies such as microrods (for 1), nanoprisms (for 2), and nanobelts (for 3). Moreover, the UV–vis absorption and emission spectra of as-prepared nanostructures were largely red-shifted, indicating J-type aggregation for all materials. Surprisingly, both 1 and 2 showed aggregation-induced emission (AIE) effect, while compound 3 showed aggregation-caused quenching (ACQ) effect. Our method to approach novel twisted azaacenes through [4 + 2] reaction could offer a new tool to develop unusual twisted conjugated materials for future optoelectronic applications.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>24741990</pmid><doi>10.1021/jo500400d</doi><tpages>8</tpages></addata></record>
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title [4 + 2] Cycloaddition Reaction To Approach Diazatwistpentacenes: Synthesis, Structures, Physical Properties, and Self-assembly
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