Largely blue-shifted emission through minor structural modifications: molecular design, synthesis, aggregation-induced emission and deep-blue OLED application
By simply introducing additional groups with different size and conjugation degree to the 2,2'-positions of BTPE, four BTPE derivatives are prepared which give blue or deep-blue EL emissions when used as emitters in non-doped OLEDs, as the result of the tuned dihedral angles of the biphenyl cor...
Gespeichert in:
| Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2014-01, Vol.50 (17), p.2136-2138 |
|---|---|
| Hauptverfasser: | , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 2138 |
|---|---|
| container_issue | 17 |
| container_start_page | 2136 |
| container_title | Chemical communications (Cambridge, England) |
| container_volume | 50 |
| creator | Huang, Jing Sun, Ning Chen, Pengyu Tang, Runli Li, Qianqian Ma, Dongge Li, Zhen |
| description | By simply introducing additional groups with different size and conjugation degree to the 2,2'-positions of BTPE, four BTPE derivatives are prepared which give blue or deep-blue EL emissions when used as emitters in non-doped OLEDs, as the result of the tuned dihedral angles of the biphenyl cores (up to ~89°), providing a new approach to design AIE luminogens with blue and deep-blue emissions. |
| doi_str_mv | 10.1039/c3cc49313j |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1513497672</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1493801577</sourcerecordid><originalsourceid>FETCH-LOGICAL-c386t-b8220dbd435cc815d50082054c80c12f48e48106db5cf5ab8866d1b0c1ffa12e3</originalsourceid><addsrcrecordid>eNqFkctOxCAUhonR6Di68QEMS2OmCgVa6s6M12SS2WjirqFAOxh6EcpiXsZnldHxspPNOeR8_OcPPwAnGF1gRIpLSaSkBcHkdQdMMMlowih_2d30rEhyQtkBOPT-FcWDGd8HBymluEizYgLeF8I12q5hZYNO_MrUo1ZQt8Z703dwXLk-NCvYmq530I8uyDE4YWHbK1MbKcZI-at4tVoGKxxU2pumm0G_7sZV7P0MiqZxuvlEE9OpIP9uEJ2Kb_SQbAzA5eL2BophsFvpI7BXC-v18bZOwfPd7dP8IVks7x_n14tEEp6NScXTFKlKUcKk5JgphhBPEaOSI4nTmnJNOUaZqpismag4zzKFqzira4FTTabg7Et3cP1b0H4soz-prRWd7oMvMcOEFnmWp_-jMQoe_znPI3r-hUrXe-90XQ7OtMKtS4zKTXTlb3QRPt3qhqrV6gf9zop8AIA5l_Y</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1493801577</pqid></control><display><type>article</type><title>Largely blue-shifted emission through minor structural modifications: molecular design, synthesis, aggregation-induced emission and deep-blue OLED application</title><source>Royal Society Of Chemistry Journals</source><source>Alma/SFX Local Collection</source><creator>Huang, Jing ; Sun, Ning ; Chen, Pengyu ; Tang, Runli ; Li, Qianqian ; Ma, Dongge ; Li, Zhen</creator><creatorcontrib>Huang, Jing ; Sun, Ning ; Chen, Pengyu ; Tang, Runli ; Li, Qianqian ; Ma, Dongge ; Li, Zhen</creatorcontrib><description>By simply introducing additional groups with different size and conjugation degree to the 2,2'-positions of BTPE, four BTPE derivatives are prepared which give blue or deep-blue EL emissions when used as emitters in non-doped OLEDs, as the result of the tuned dihedral angles of the biphenyl cores (up to ~89°), providing a new approach to design AIE luminogens with blue and deep-blue emissions.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/c3cc49313j</identifier><identifier>PMID: 24419269</identifier><language>eng</language><publisher>England</publisher><subject>Conjugation ; Derivatives ; Emission ; Emitters ; Synthesis</subject><ispartof>Chemical communications (Cambridge, England), 2014-01, Vol.50 (17), p.2136-2138</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-b8220dbd435cc815d50082054c80c12f48e48106db5cf5ab8866d1b0c1ffa12e3</citedby><cites>FETCH-LOGICAL-c386t-b8220dbd435cc815d50082054c80c12f48e48106db5cf5ab8866d1b0c1ffa12e3</cites></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/24419269$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Jing</creatorcontrib><creatorcontrib>Sun, Ning</creatorcontrib><creatorcontrib>Chen, Pengyu</creatorcontrib><creatorcontrib>Tang, Runli</creatorcontrib><creatorcontrib>Li, Qianqian</creatorcontrib><creatorcontrib>Ma, Dongge</creatorcontrib><creatorcontrib>Li, Zhen</creatorcontrib><title>Largely blue-shifted emission through minor structural modifications: molecular design, synthesis, aggregation-induced emission and deep-blue OLED application</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>By simply introducing additional groups with different size and conjugation degree to the 2,2'-positions of BTPE, four BTPE derivatives are prepared which give blue or deep-blue EL emissions when used as emitters in non-doped OLEDs, as the result of the tuned dihedral angles of the biphenyl cores (up to ~89°), providing a new approach to design AIE luminogens with blue and deep-blue emissions.</description><subject>Conjugation</subject><subject>Derivatives</subject><subject>Emission</subject><subject>Emitters</subject><subject>Synthesis</subject><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkctOxCAUhonR6Di68QEMS2OmCgVa6s6M12SS2WjirqFAOxh6EcpiXsZnldHxspPNOeR8_OcPPwAnGF1gRIpLSaSkBcHkdQdMMMlowih_2d30rEhyQtkBOPT-FcWDGd8HBymluEizYgLeF8I12q5hZYNO_MrUo1ZQt8Z703dwXLk-NCvYmq530I8uyDE4YWHbK1MbKcZI-at4tVoGKxxU2pumm0G_7sZV7P0MiqZxuvlEE9OpIP9uEJ2Kb_SQbAzA5eL2BophsFvpI7BXC-v18bZOwfPd7dP8IVks7x_n14tEEp6NScXTFKlKUcKk5JgphhBPEaOSI4nTmnJNOUaZqpismag4zzKFqzira4FTTabg7Et3cP1b0H4soz-prRWd7oMvMcOEFnmWp_-jMQoe_znPI3r-hUrXe-90XQ7OtMKtS4zKTXTlb3QRPt3qhqrV6gf9zop8AIA5l_Y</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Huang, Jing</creator><creator>Sun, Ning</creator><creator>Chen, Pengyu</creator><creator>Tang, Runli</creator><creator>Li, Qianqian</creator><creator>Ma, Dongge</creator><creator>Li, Zhen</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7SP</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20140101</creationdate><title>Largely blue-shifted emission through minor structural modifications: molecular design, synthesis, aggregation-induced emission and deep-blue OLED application</title><author>Huang, Jing ; Sun, Ning ; Chen, Pengyu ; Tang, Runli ; Li, Qianqian ; Ma, Dongge ; Li, Zhen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-b8220dbd435cc815d50082054c80c12f48e48106db5cf5ab8866d1b0c1ffa12e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Conjugation</topic><topic>Derivatives</topic><topic>Emission</topic><topic>Emitters</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Jing</creatorcontrib><creatorcontrib>Sun, Ning</creatorcontrib><creatorcontrib>Chen, Pengyu</creatorcontrib><creatorcontrib>Tang, Runli</creatorcontrib><creatorcontrib>Li, Qianqian</creatorcontrib><creatorcontrib>Ma, Dongge</creatorcontrib><creatorcontrib>Li, Zhen</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Electronics & Communications Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Jing</au><au>Sun, Ning</au><au>Chen, Pengyu</au><au>Tang, Runli</au><au>Li, Qianqian</au><au>Ma, Dongge</au><au>Li, Zhen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Largely blue-shifted emission through minor structural modifications: molecular design, synthesis, aggregation-induced emission and deep-blue OLED application</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>50</volume><issue>17</issue><spage>2136</spage><epage>2138</epage><pages>2136-2138</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>By simply introducing additional groups with different size and conjugation degree to the 2,2'-positions of BTPE, four BTPE derivatives are prepared which give blue or deep-blue EL emissions when used as emitters in non-doped OLEDs, as the result of the tuned dihedral angles of the biphenyl cores (up to ~89°), providing a new approach to design AIE luminogens with blue and deep-blue emissions.</abstract><cop>England</cop><pmid>24419269</pmid><doi>10.1039/c3cc49313j</doi><tpages>3</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1359-7345 |
| ispartof | Chemical communications (Cambridge, England), 2014-01, Vol.50 (17), p.2136-2138 |
| issn | 1359-7345 1364-548X |
| language | eng |
| recordid | cdi_proquest_miscellaneous_1513497672 |
| source | Royal Society Of Chemistry Journals; Alma/SFX Local Collection |
| subjects | Conjugation Derivatives Emission Emitters Synthesis |
| title | Largely blue-shifted emission through minor structural modifications: molecular design, synthesis, aggregation-induced emission and deep-blue OLED application |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T21%3A44%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Largely%20blue-shifted%20emission%20through%20minor%20structural%20modifications:%20molecular%20design,%20synthesis,%20aggregation-induced%20emission%20and%20deep-blue%20OLED%20application&rft.jtitle=Chemical%20communications%20(Cambridge,%20England)&rft.au=Huang,%20Jing&rft.date=2014-01-01&rft.volume=50&rft.issue=17&rft.spage=2136&rft.epage=2138&rft.pages=2136-2138&rft.issn=1359-7345&rft.eissn=1364-548X&rft_id=info:doi/10.1039/c3cc49313j&rft_dat=%3Cproquest_cross%3E1493801577%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1493801577&rft_id=info:pmid/24419269&rfr_iscdi=true |