Cyclic Triimidazole Derivatives: Intriguing Examples of Multiple Emissions and Ultralong Phosphorescence at Room Temperature
The performance of solid luminogens depends on both their inherent electronic properties and their packing status. Intermolecular interactions have been exploited to achieve persistent room‐temperature phosphorescence (RTP) from organic molecules. However, the design of organic materials with bright...
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Published in: | Angewandte Chemie International Edition Vol. 56; no. 51; pp. 16302 - 16307 |
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Abstract | The performance of solid luminogens depends on both their inherent electronic properties and their packing status. Intermolecular interactions have been exploited to achieve persistent room‐temperature phosphorescence (RTP) from organic molecules. However, the design of organic materials with bright RTP and the rationalization of the role of interchromophoric electronic coupling remain challenging tasks. Cyclic triimidazole has been shown to be a promising scaffold for such purposes owing to its crystallization‐induced room‐temperature ultralong phosphorescence (RTUP), which has been associated with H‐aggregation. Herein, we report three triimidazole derivatives as significant examples of multifaceted emission. In particular, dual fluorescence, RTUP, and phosphorescence from the molecular and supramolecular units were observed. H‐aggregation is responsible for the red RTUP, and Br substituents favor yellow molecular phosphorescence while halogen‐bonded Br⋅⋅⋅Br tetrameric units are involved in the blue‐green phosphorescence.
Three triimidazole derivatives were synthesized that display multiple emissions covering dual fluorescence, room‐temperature ultralong phosphorescence (RTUP), and phosphorescence from the molecular and supramolecular units. H‐aggregation is responsible for the red RTUP, Br substituents favor yellow molecular phosphorescence, and halogen‐bonded Br⋅⋅⋅Br tetrameric units are involved in the blue‐green phosphorescence. |
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AbstractList | The performance of solid luminogens depends on both their inherent electronic properties and their packing status. Intermolecular interactions have been exploited to achieve persistent room-temperature phosphorescence (RTP) from organic molecules. However, the design of organic materials with bright RTP and the rationalization of the role of interchromophoric electronic coupling remain challenging tasks. Cyclic triimidazole has been shown to be a promising scaffold for such purposes owing to its crystallization-induced room-temperature ultralong phosphorescence (RTUP), which has been associated with H-aggregation. Herein, we report three triimidazole derivatives as significant examples of multifaceted emission. In particular, dual fluorescence, RTUP, and phosphorescence from the molecular and supramolecular units were observed. H-aggregation is responsible for the red RTUP, and Br substituents favor yellow molecular phosphorescence while halogen-bonded Br⋅⋅⋅Br tetrameric units are involved in the blue-green phosphorescence. The performance of solid luminogens depends on both their inherent electronic properties and their packing status. Intermolecular interactions have been exploited to achieve persistent room-temperature phosphorescence (RTP) from organic molecules. However, the design of organic materials with bright RTP and the rationalization of the role of interchromophoric electronic coupling remain challenging tasks. Cyclic triimidazole has been shown to be a promising scaffold for such purposes owing to its crystallization-induced room-temperature ultralong phosphorescence (RTUP), which has been associated with H-aggregation. Herein, we report three triimidazole derivatives as significant examples of multifaceted emission. In particular, dual fluorescence, RTUP, and phosphorescence from the molecular and supramolecular units were observed. H-aggregation is responsible for the red RTUP, and Br substituents favor yellow molecular phosphorescence while halogen-bonded BrBr tetrameric units are involved in the blue-green phosphorescence. The performance of solid luminogens depends on both their inherent electronic properties and their packing status. Intermolecular interactions have been exploited to achieve persistent room‐temperature phosphorescence (RTP) from organic molecules. However, the design of organic materials with bright RTP and the rationalization of the role of interchromophoric electronic coupling remain challenging tasks. Cyclic triimidazole has been shown to be a promising scaffold for such purposes owing to its crystallization‐induced room‐temperature ultralong phosphorescence (RTUP), which has been associated with H‐aggregation. Herein, we report three triimidazole derivatives as significant examples of multifaceted emission. In particular, dual fluorescence, RTUP, and phosphorescence from the molecular and supramolecular units were observed. H‐aggregation is responsible for the red RTUP, and Br substituents favor yellow molecular phosphorescence while halogen‐bonded Br⋅⋅⋅Br tetrameric units are involved in the blue‐green phosphorescence. Three triimidazole derivatives were synthesized that display multiple emissions covering dual fluorescence, room‐temperature ultralong phosphorescence (RTUP), and phosphorescence from the molecular and supramolecular units. H‐aggregation is responsible for the red RTUP, Br substituents favor yellow molecular phosphorescence, and halogen‐bonded Br⋅⋅⋅Br tetrameric units are involved in the blue‐green phosphorescence. |
Author | Carlucci, Lucia Previtali, Andrea Pavanello, Alessandro Marinotto, Daniele Righetto, Stefania Lucenti, Elena Forni, Alessandra Botta, Chiara Cariati, Elena Giannini, Clelia |
Author_xml | – sequence: 1 givenname: Elena orcidid: 0000-0002-2418-7565 surname: Lucenti fullname: Lucenti, Elena organization: ISTM-CNR – sequence: 2 givenname: Alessandra orcidid: 0000-0002-5020-5544 surname: Forni fullname: Forni, Alessandra email: alessandra.forni@istm.cnr.it organization: ISTM-CNR – sequence: 3 givenname: Chiara orcidid: 0000-0001-8722-0417 surname: Botta fullname: Botta, Chiara email: chiara.botta@ismac.cnr.it organization: ISMAC-CNR – sequence: 4 givenname: Lucia orcidid: 0000-0001-5856-5280 surname: Carlucci fullname: Carlucci, Lucia organization: Università degli Studi di Milano and INSTM RU – sequence: 5 givenname: Clelia orcidid: 0000-0003-3376-8350 surname: Giannini fullname: Giannini, Clelia organization: Università degli Studi di Milano and INSTM RU – sequence: 6 givenname: Daniele orcidid: 0000-0002-4490-8825 surname: Marinotto fullname: Marinotto, Daniele organization: Università degli Studi di Milano and INSTM RU – sequence: 7 givenname: Alessandro surname: Pavanello fullname: Pavanello, Alessandro organization: Università degli Studi di Milano and INSTM RU – sequence: 8 givenname: Andrea orcidid: 0000-0001-9537-8652 surname: Previtali fullname: Previtali, Andrea organization: Università degli Studi di Milano and INSTM RU – sequence: 9 givenname: Stefania orcidid: 0000-0002-2537-3220 surname: Righetto fullname: Righetto, Stefania organization: Università degli Studi di Milano and INSTM RU – sequence: 10 givenname: Elena orcidid: 0000-0003-1781-0360 surname: Cariati fullname: Cariati, Elena email: elena.cariati@unimi.it organization: Università degli Studi di Milano and INSTM RU |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29106768$$D View this record in MEDLINE/PubMed |
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Keywords | time-resolved spectroscopy phosphorescence H-aggregates photophysics halogen bonding |
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SubjectTerms | Agglomeration Chemical bonds Coupling (molecular) Crystallization Derivatives Emissions Fluorescence H-aggregates halogen bonding Organic chemistry Organic materials Packing Phosphorescence photophysics Room temperature Temperature effects time-resolved spectroscopy |
Title | Cyclic Triimidazole Derivatives: Intriguing Examples of Multiple Emissions and Ultralong Phosphorescence at Room Temperature |
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