Cargando…

Achieving highly efficient aggregation-induced emission, reversible and irreversible photochromism by heavy halogen-regulated photophysics and D–A molecular pattern-controlled photochemistry of through-space conjugated luminogens

It is extremely challenging but desirable to regulate the photophysical and photochemical processes of aggregation-induced emission luminogens (AIEgens) in distinct states in a controllable manner. Herein, we design two groups of AIEgens based on a triphenylacrylonitrile (TPAN) skeleton with through...

Descripción completa

Detalles Bibliográficos
Autores principales: Xiong, Zuping, Zhang, Xiaoxiao, Liu, Longxiang, Zhu, Qiaozhi, Wang, Zhenni, Feng, Hui, Qian, Zhaosheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372539/
https://www.ncbi.nlm.nih.gov/pubmed/34476056
http://dx.doi.org/10.1039/d1sc02168k
_version_ 1783739814905905152
author Xiong, Zuping
Zhang, Xiaoxiao
Liu, Longxiang
Zhu, Qiaozhi
Wang, Zhenni
Feng, Hui
Qian, Zhaosheng
author_facet Xiong, Zuping
Zhang, Xiaoxiao
Liu, Longxiang
Zhu, Qiaozhi
Wang, Zhenni
Feng, Hui
Qian, Zhaosheng
author_sort Xiong, Zuping
collection PubMed
description It is extremely challenging but desirable to regulate the photophysical and photochemical processes of aggregation-induced emission luminogens (AIEgens) in distinct states in a controllable manner. Herein, we design two groups of AIEgens based on a triphenylacrylonitrile (TPAN) skeleton with through-space conjugation (TSC) property, demonstrate controlled regulation of photophysical emission efficiency/color and photochemical photochromic and photoactivatable fluorescence behaviours of these compounds, and further validate design principles to achieve highly efficient and emission-tuning AIEgens and to accomplish photo-dependent color switches and fluorescence changes. It is surprisingly found that the introduction of heavy halogens like bromine into a TPAN skeleton dramatically enhances the emission efficiency, and such an abnormal phenomenon against the heavy-atom effect is attributed to the specific through-space conjugation nature of the AIE-active skeleton, effective intermolecular halogen-bond-induced restriction of intramolecular motions, and heavy atom-induced vibration reduction. The incorporation of two electron-donating amino groups into the TPAN skeleton cause the luminogens to undergo a bathochromic shifted emission due to the formation of a D–A pattern. Apart from the regulation of photophysical processes in the solid state, the construction of the D–A pattern in luminogens also results in extremely different photochemical reactions accompanying reversible/irreversible photochromism and photoactivatable fluorescence phenomena in a dispersed state. It is revealed that photo-triggered cyclization and decyclization reactions dominantly contribute to reversible photochromism of the TPAN family, and the photo-induced cyclization–dehydrogenation reaction is responsible for the irreversible color changes and photoactivatable fluorescence behaviours of the NTPAN family. The demonstrations of multiple-mode signaling in photoswitchable patterning and information encryption highlight the importance of controlled regulation of photophysics and photochemistry of fused chromic and AIE-active luminogens in distinct states.
format Online
Article
Text
id pubmed-8372539
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-83725392021-09-01 Achieving highly efficient aggregation-induced emission, reversible and irreversible photochromism by heavy halogen-regulated photophysics and D–A molecular pattern-controlled photochemistry of through-space conjugated luminogens Xiong, Zuping Zhang, Xiaoxiao Liu, Longxiang Zhu, Qiaozhi Wang, Zhenni Feng, Hui Qian, Zhaosheng Chem Sci Chemistry It is extremely challenging but desirable to regulate the photophysical and photochemical processes of aggregation-induced emission luminogens (AIEgens) in distinct states in a controllable manner. Herein, we design two groups of AIEgens based on a triphenylacrylonitrile (TPAN) skeleton with through-space conjugation (TSC) property, demonstrate controlled regulation of photophysical emission efficiency/color and photochemical photochromic and photoactivatable fluorescence behaviours of these compounds, and further validate design principles to achieve highly efficient and emission-tuning AIEgens and to accomplish photo-dependent color switches and fluorescence changes. It is surprisingly found that the introduction of heavy halogens like bromine into a TPAN skeleton dramatically enhances the emission efficiency, and such an abnormal phenomenon against the heavy-atom effect is attributed to the specific through-space conjugation nature of the AIE-active skeleton, effective intermolecular halogen-bond-induced restriction of intramolecular motions, and heavy atom-induced vibration reduction. The incorporation of two electron-donating amino groups into the TPAN skeleton cause the luminogens to undergo a bathochromic shifted emission due to the formation of a D–A pattern. Apart from the regulation of photophysical processes in the solid state, the construction of the D–A pattern in luminogens also results in extremely different photochemical reactions accompanying reversible/irreversible photochromism and photoactivatable fluorescence phenomena in a dispersed state. It is revealed that photo-triggered cyclization and decyclization reactions dominantly contribute to reversible photochromism of the TPAN family, and the photo-induced cyclization–dehydrogenation reaction is responsible for the irreversible color changes and photoactivatable fluorescence behaviours of the NTPAN family. The demonstrations of multiple-mode signaling in photoswitchable patterning and information encryption highlight the importance of controlled regulation of photophysics and photochemistry of fused chromic and AIE-active luminogens in distinct states. The Royal Society of Chemistry 2021-07-05 /pmc/articles/PMC8372539/ /pubmed/34476056 http://dx.doi.org/10.1039/d1sc02168k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Xiong, Zuping
Zhang, Xiaoxiao
Liu, Longxiang
Zhu, Qiaozhi
Wang, Zhenni
Feng, Hui
Qian, Zhaosheng
Achieving highly efficient aggregation-induced emission, reversible and irreversible photochromism by heavy halogen-regulated photophysics and D–A molecular pattern-controlled photochemistry of through-space conjugated luminogens
title Achieving highly efficient aggregation-induced emission, reversible and irreversible photochromism by heavy halogen-regulated photophysics and D–A molecular pattern-controlled photochemistry of through-space conjugated luminogens
title_full Achieving highly efficient aggregation-induced emission, reversible and irreversible photochromism by heavy halogen-regulated photophysics and D–A molecular pattern-controlled photochemistry of through-space conjugated luminogens
title_fullStr Achieving highly efficient aggregation-induced emission, reversible and irreversible photochromism by heavy halogen-regulated photophysics and D–A molecular pattern-controlled photochemistry of through-space conjugated luminogens
title_full_unstemmed Achieving highly efficient aggregation-induced emission, reversible and irreversible photochromism by heavy halogen-regulated photophysics and D–A molecular pattern-controlled photochemistry of through-space conjugated luminogens
title_short Achieving highly efficient aggregation-induced emission, reversible and irreversible photochromism by heavy halogen-regulated photophysics and D–A molecular pattern-controlled photochemistry of through-space conjugated luminogens
title_sort achieving highly efficient aggregation-induced emission, reversible and irreversible photochromism by heavy halogen-regulated photophysics and d–a molecular pattern-controlled photochemistry of through-space conjugated luminogens
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372539/
https://www.ncbi.nlm.nih.gov/pubmed/34476056
http://dx.doi.org/10.1039/d1sc02168k
work_keys_str_mv AT xiongzuping achievinghighlyefficientaggregationinducedemissionreversibleandirreversiblephotochromismbyheavyhalogenregulatedphotophysicsanddamolecularpatterncontrolledphotochemistryofthroughspaceconjugatedluminogens
AT zhangxiaoxiao achievinghighlyefficientaggregationinducedemissionreversibleandirreversiblephotochromismbyheavyhalogenregulatedphotophysicsanddamolecularpatterncontrolledphotochemistryofthroughspaceconjugatedluminogens
AT liulongxiang achievinghighlyefficientaggregationinducedemissionreversibleandirreversiblephotochromismbyheavyhalogenregulatedphotophysicsanddamolecularpatterncontrolledphotochemistryofthroughspaceconjugatedluminogens
AT zhuqiaozhi achievinghighlyefficientaggregationinducedemissionreversibleandirreversiblephotochromismbyheavyhalogenregulatedphotophysicsanddamolecularpatterncontrolledphotochemistryofthroughspaceconjugatedluminogens
AT wangzhenni achievinghighlyefficientaggregationinducedemissionreversibleandirreversiblephotochromismbyheavyhalogenregulatedphotophysicsanddamolecularpatterncontrolledphotochemistryofthroughspaceconjugatedluminogens
AT fenghui achievinghighlyefficientaggregationinducedemissionreversibleandirreversiblephotochromismbyheavyhalogenregulatedphotophysicsanddamolecularpatterncontrolledphotochemistryofthroughspaceconjugatedluminogens
AT qianzhaosheng achievinghighlyefficientaggregationinducedemissionreversibleandirreversiblephotochromismbyheavyhalogenregulatedphotophysicsanddamolecularpatterncontrolledphotochemistryofthroughspaceconjugatedluminogens