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Unravelling the intricate photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine AIE and RTP polymorphs
The development of purely organic materials showing multicolor fluorescent and phosphorescent behaviour represents a formidable challenge in view of practical applications. Herein the rich photophysical behaviour of 3-(pyridin-2-yl)triimidazotriazine (TT-Py) organic molecule, comprising excitation-d...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504899/ https://www.ncbi.nlm.nih.gov/pubmed/33033610 http://dx.doi.org/10.1039/d0sc02459g |
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author | Lucenti, Elena Forni, Alessandra Previtali, Andrea Marinotto, Daniele Malpicci, Daniele Righetto, Stefania Giannini, Clelia Virgili, Tersilla Kabacinski, Piotr Ganzer, Lucia Giovanella, Umberto Botta, Chiara Cariati, Elena |
author_facet | Lucenti, Elena Forni, Alessandra Previtali, Andrea Marinotto, Daniele Malpicci, Daniele Righetto, Stefania Giannini, Clelia Virgili, Tersilla Kabacinski, Piotr Ganzer, Lucia Giovanella, Umberto Botta, Chiara Cariati, Elena |
author_sort | Lucenti, Elena |
collection | PubMed |
description | The development of purely organic materials showing multicolor fluorescent and phosphorescent behaviour represents a formidable challenge in view of practical applications. Herein the rich photophysical behaviour of 3-(pyridin-2-yl)triimidazotriazine (TT-Py) organic molecule, comprising excitation-dependent fluorescence and phosphorescence under ambient conditions in both blended films and the crystalline phase, is investigated by means of steady state, time resolved and ultrafast spectroscopies and interpreted on the basis of X-ray diffraction studies and DFT/TDDFT calculations. In particular, by proper excitation wavelength, dual fluorescence and dual phosphorescence of molecular origin can be observed together with low energy phosphorescences resulting from aggregate species. It is demonstrated that the multiple emission properties originate from the copresence, in the investigated system, of an extended polycyclic nitrogen-rich moiety (TT), strongly rigidified by π–π stacking interactions and short C–H···N hydrogen bonds, and a fragment (Py) having partial conformational freedom. |
format | Online Article Text |
id | pubmed-7504899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-75048992020-10-07 Unravelling the intricate photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine AIE and RTP polymorphs Lucenti, Elena Forni, Alessandra Previtali, Andrea Marinotto, Daniele Malpicci, Daniele Righetto, Stefania Giannini, Clelia Virgili, Tersilla Kabacinski, Piotr Ganzer, Lucia Giovanella, Umberto Botta, Chiara Cariati, Elena Chem Sci Chemistry The development of purely organic materials showing multicolor fluorescent and phosphorescent behaviour represents a formidable challenge in view of practical applications. Herein the rich photophysical behaviour of 3-(pyridin-2-yl)triimidazotriazine (TT-Py) organic molecule, comprising excitation-dependent fluorescence and phosphorescence under ambient conditions in both blended films and the crystalline phase, is investigated by means of steady state, time resolved and ultrafast spectroscopies and interpreted on the basis of X-ray diffraction studies and DFT/TDDFT calculations. In particular, by proper excitation wavelength, dual fluorescence and dual phosphorescence of molecular origin can be observed together with low energy phosphorescences resulting from aggregate species. It is demonstrated that the multiple emission properties originate from the copresence, in the investigated system, of an extended polycyclic nitrogen-rich moiety (TT), strongly rigidified by π–π stacking interactions and short C–H···N hydrogen bonds, and a fragment (Py) having partial conformational freedom. Royal Society of Chemistry 2020-06-09 /pmc/articles/PMC7504899/ /pubmed/33033610 http://dx.doi.org/10.1039/d0sc02459g Text en This journal is © The Royal Society of Chemistry 2020 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Lucenti, Elena Forni, Alessandra Previtali, Andrea Marinotto, Daniele Malpicci, Daniele Righetto, Stefania Giannini, Clelia Virgili, Tersilla Kabacinski, Piotr Ganzer, Lucia Giovanella, Umberto Botta, Chiara Cariati, Elena Unravelling the intricate photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine AIE and RTP polymorphs |
title | Unravelling the intricate photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine AIE and RTP polymorphs
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title_full | Unravelling the intricate photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine AIE and RTP polymorphs
|
title_fullStr | Unravelling the intricate photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine AIE and RTP polymorphs
|
title_full_unstemmed | Unravelling the intricate photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine AIE and RTP polymorphs
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title_short | Unravelling the intricate photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine AIE and RTP polymorphs
|
title_sort | unravelling the intricate photophysical behavior of 3-(pyridin-2-yl)triimidazotriazine aie and rtp polymorphs |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504899/ https://www.ncbi.nlm.nih.gov/pubmed/33033610 http://dx.doi.org/10.1039/d0sc02459g |
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