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Intrinsic and Extrinsic Heavy‐Atom Effects on the Multifaceted Emissive Behavior of Cyclic Triimidazole
Considering that heavy halogen atoms can be used to tune the emissive properties of organic luminogens, the understanding of their role in photophysics is fundamental for materials engineering. Here, the extrinsic and intrinsic heavy‐atom effects on the photophysics of organic crystals were separate...
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Published in: | Chemistry : a European journal 2019-02, Vol.25 (10), p.2452-2456 |
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creator | Lucenti, Elena Forni, Alessandra Botta, Chiara Giannini, Clelia Malpicci, Daniele Marinotto, Daniele Previtali, Andrea Righetto, Stefania Cariati, Elena |
description | Considering that heavy halogen atoms can be used to tune the emissive properties of organic luminogens, the understanding of their role in photophysics is fundamental for materials engineering. Here, the extrinsic and intrinsic heavy‐atom effects on the photophysics of organic crystals were separately evaluated by comparing cyclic triimidazole (TT) with its monoiodo derivative (TTI) and its co‐crystal with diiodotetrafluorobenzene (TTCo). Crystals of TT showed room‐temperature ultralong phosphorescence (RTUP) originated from H‐aggregation. TTI and TTCo displayed two additional long‐lived components, the origin of which is elucidated through single‐crystal X‐ray and DFT/TDDFT studies. The results highlight the different effects of the I atom on the three phosphorescent emissions. Intrinsic heavy‐atom effects play a major role on molecular phosphorescence, which is displayed at room temperature only for TTI. The H‐aggregate RTUP and the I⋅⋅⋅N XB‐induced (XB=halogen bond) phosphorescence on the other side depend only on packing features.
Heavy halogen atoms can tune the emissive properties of organic luminogens both extrinsically and intrinsically. Here, the two effects were investigated by comparing cyclic triimidazole (TT) with its monoiododerivative (TTI), and its co‐crystal with diiodotetrafluorobenzene (TTCo). TTI showed a unique XB‐supported (XB=halogen bond) quadruple‐helix motif in its crystal structure. |
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Heavy halogen atoms can tune the emissive properties of organic luminogens both extrinsically and intrinsically. Here, the two effects were investigated by comparing cyclic triimidazole (TT) with its monoiododerivative (TTI), and its co‐crystal with diiodotetrafluorobenzene (TTCo). TTI showed a unique XB‐supported (XB=halogen bond) quadruple‐helix motif in its crystal structure.</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.201804980</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Chemistry ; co-crystals ; Crystals ; halogen bonding ; Materials engineering ; Organic crystals ; Phosphorescence ; photophysics ; time-resolved spectroscopy</subject><ispartof>Chemistry : a European journal, 2019-02, Vol.25 (10), p.2452-2456</ispartof><rights>2019 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3900-4cf8be054dcd106ac0ff04e697ac23aab8071a30205873e3e51d049b51a86aac3</citedby><cites>FETCH-LOGICAL-c3900-4cf8be054dcd106ac0ff04e697ac23aab8071a30205873e3e51d049b51a86aac3</cites><orcidid>0000-0001-9537-8652 ; 0000-0001-8722-0417 ; 0000-0003-1781-0360 ; 0000-0002-5020-5544 ; 0000-0002-2418-7565 ; 0000-0002-4490-8825 ; 0000-0002-2537-3220 ; 0000-0003-3376-8350</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Lucenti, Elena</creatorcontrib><creatorcontrib>Forni, Alessandra</creatorcontrib><creatorcontrib>Botta, Chiara</creatorcontrib><creatorcontrib>Giannini, Clelia</creatorcontrib><creatorcontrib>Malpicci, Daniele</creatorcontrib><creatorcontrib>Marinotto, Daniele</creatorcontrib><creatorcontrib>Previtali, Andrea</creatorcontrib><creatorcontrib>Righetto, Stefania</creatorcontrib><creatorcontrib>Cariati, Elena</creatorcontrib><title>Intrinsic and Extrinsic Heavy‐Atom Effects on the Multifaceted Emissive Behavior of Cyclic Triimidazole</title><title>Chemistry : a European journal</title><description>Considering that heavy halogen atoms can be used to tune the emissive properties of organic luminogens, the understanding of their role in photophysics is fundamental for materials engineering. Here, the extrinsic and intrinsic heavy‐atom effects on the photophysics of organic crystals were separately evaluated by comparing cyclic triimidazole (TT) with its monoiodo derivative (TTI) and its co‐crystal with diiodotetrafluorobenzene (TTCo). Crystals of TT showed room‐temperature ultralong phosphorescence (RTUP) originated from H‐aggregation. TTI and TTCo displayed two additional long‐lived components, the origin of which is elucidated through single‐crystal X‐ray and DFT/TDDFT studies. The results highlight the different effects of the I atom on the three phosphorescent emissions. Intrinsic heavy‐atom effects play a major role on molecular phosphorescence, which is displayed at room temperature only for TTI. The H‐aggregate RTUP and the I⋅⋅⋅N XB‐induced (XB=halogen bond) phosphorescence on the other side depend only on packing features.
Heavy halogen atoms can tune the emissive properties of organic luminogens both extrinsically and intrinsically. Here, the two effects were investigated by comparing cyclic triimidazole (TT) with its monoiododerivative (TTI), and its co‐crystal with diiodotetrafluorobenzene (TTCo). TTI showed a unique XB‐supported (XB=halogen bond) quadruple‐helix motif in its crystal structure.</description><subject>Chemistry</subject><subject>co-crystals</subject><subject>Crystals</subject><subject>halogen bonding</subject><subject>Materials engineering</subject><subject>Organic crystals</subject><subject>Phosphorescence</subject><subject>photophysics</subject><subject>time-resolved spectroscopy</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkD1PwzAQhi0EEqWwMltiYUk5x3E-xlIVitSKBebIdc6qURKDnRTKxE_gN_JLcFU-JBam00nP8-ruJeSUwYgBxBdqhc0oBpZDUuSwRwZMxCziWSr2yQCKJItSwYtDcuT9AwAUKecDYm7azpnWG0VlW9Hpy_c2Q7nefLy9jzvb0KnWqDpPbUu7FdJFX3dGS4UdBqUx3ps10ktcybWxjlpNJxtVh5A7Z0xjKvlqazwmB1rWHk--5pDcX03vJrNofnt9MxnPI8ULgChROl8iiKRSFYNUKtAaEkyLTKqYS7nMIWOSQwwizzhyFKwKDy8Fk3kqpeJDcr7LfXT2qUffleFAhXUtW7S9L2Mm8jgRSQIBPfuDPtjeteG6QAWoyFmcBWq0o5Sz3jvU5aMzjXSbkkG5bb7cNl_-NB-EYic8mxo3_9DlZDZd_LqfzP6I5g</recordid><startdate>20190218</startdate><enddate>20190218</enddate><creator>Lucenti, Elena</creator><creator>Forni, Alessandra</creator><creator>Botta, Chiara</creator><creator>Giannini, Clelia</creator><creator>Malpicci, Daniele</creator><creator>Marinotto, Daniele</creator><creator>Previtali, Andrea</creator><creator>Righetto, Stefania</creator><creator>Cariati, Elena</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9537-8652</orcidid><orcidid>https://orcid.org/0000-0001-8722-0417</orcidid><orcidid>https://orcid.org/0000-0003-1781-0360</orcidid><orcidid>https://orcid.org/0000-0002-5020-5544</orcidid><orcidid>https://orcid.org/0000-0002-2418-7565</orcidid><orcidid>https://orcid.org/0000-0002-4490-8825</orcidid><orcidid>https://orcid.org/0000-0002-2537-3220</orcidid><orcidid>https://orcid.org/0000-0003-3376-8350</orcidid></search><sort><creationdate>20190218</creationdate><title>Intrinsic and Extrinsic Heavy‐Atom Effects on the Multifaceted Emissive Behavior of Cyclic Triimidazole</title><author>Lucenti, Elena ; Forni, Alessandra ; Botta, Chiara ; Giannini, Clelia ; Malpicci, Daniele ; Marinotto, Daniele ; Previtali, Andrea ; Righetto, Stefania ; Cariati, Elena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3900-4cf8be054dcd106ac0ff04e697ac23aab8071a30205873e3e51d049b51a86aac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Chemistry</topic><topic>co-crystals</topic><topic>Crystals</topic><topic>halogen bonding</topic><topic>Materials engineering</topic><topic>Organic crystals</topic><topic>Phosphorescence</topic><topic>photophysics</topic><topic>time-resolved spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lucenti, Elena</creatorcontrib><creatorcontrib>Forni, Alessandra</creatorcontrib><creatorcontrib>Botta, Chiara</creatorcontrib><creatorcontrib>Giannini, Clelia</creatorcontrib><creatorcontrib>Malpicci, Daniele</creatorcontrib><creatorcontrib>Marinotto, Daniele</creatorcontrib><creatorcontrib>Previtali, Andrea</creatorcontrib><creatorcontrib>Righetto, Stefania</creatorcontrib><creatorcontrib>Cariati, Elena</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lucenti, Elena</au><au>Forni, Alessandra</au><au>Botta, Chiara</au><au>Giannini, Clelia</au><au>Malpicci, Daniele</au><au>Marinotto, Daniele</au><au>Previtali, Andrea</au><au>Righetto, Stefania</au><au>Cariati, Elena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intrinsic and Extrinsic Heavy‐Atom Effects on the Multifaceted Emissive Behavior of Cyclic Triimidazole</atitle><jtitle>Chemistry : a European journal</jtitle><date>2019-02-18</date><risdate>2019</risdate><volume>25</volume><issue>10</issue><spage>2452</spage><epage>2456</epage><pages>2452-2456</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>Considering that heavy halogen atoms can be used to tune the emissive properties of organic luminogens, the understanding of their role in photophysics is fundamental for materials engineering. Here, the extrinsic and intrinsic heavy‐atom effects on the photophysics of organic crystals were separately evaluated by comparing cyclic triimidazole (TT) with its monoiodo derivative (TTI) and its co‐crystal with diiodotetrafluorobenzene (TTCo). Crystals of TT showed room‐temperature ultralong phosphorescence (RTUP) originated from H‐aggregation. TTI and TTCo displayed two additional long‐lived components, the origin of which is elucidated through single‐crystal X‐ray and DFT/TDDFT studies. The results highlight the different effects of the I atom on the three phosphorescent emissions. Intrinsic heavy‐atom effects play a major role on molecular phosphorescence, which is displayed at room temperature only for TTI. The H‐aggregate RTUP and the I⋅⋅⋅N XB‐induced (XB=halogen bond) phosphorescence on the other side depend only on packing features.
Heavy halogen atoms can tune the emissive properties of organic luminogens both extrinsically and intrinsically. Here, the two effects were investigated by comparing cyclic triimidazole (TT) with its monoiododerivative (TTI), and its co‐crystal with diiodotetrafluorobenzene (TTCo). TTI showed a unique XB‐supported (XB=halogen bond) quadruple‐helix motif in its crystal structure.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/chem.201804980</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0001-9537-8652</orcidid><orcidid>https://orcid.org/0000-0001-8722-0417</orcidid><orcidid>https://orcid.org/0000-0003-1781-0360</orcidid><orcidid>https://orcid.org/0000-0002-5020-5544</orcidid><orcidid>https://orcid.org/0000-0002-2418-7565</orcidid><orcidid>https://orcid.org/0000-0002-4490-8825</orcidid><orcidid>https://orcid.org/0000-0002-2537-3220</orcidid><orcidid>https://orcid.org/0000-0003-3376-8350</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Chemistry co-crystals Crystals halogen bonding Materials engineering Organic crystals Phosphorescence photophysics time-resolved spectroscopy |
title | Intrinsic and Extrinsic Heavy‐Atom Effects on the Multifaceted Emissive Behavior of Cyclic Triimidazole |
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