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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2020
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.
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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
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
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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