Structure-property relationship on aggregation-induced emission properties of simple azine-based AIEgens and its application in metal ions detection

In recent twenty years, aggregation-induced emission (AIE), due to its excellent application prospect, has aroused widespread interests. The development of novel and easy to make AIE luminogens (AIEgens) is an attractive subject. For this purpose, it is very important to study the structure-property...

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Published inChinese chemical letters Vol. 34; no. 5; p. 107792
Main Authors Sun, Xiao-Mei, Liu, Juan, Li, Zhao-Hui, Fu, Yong-Peng, Huang, Ting-Ting, Tang, Zhong-Di, Shi, Bingbing, Yao, Hong, Wei, Tai-Bao, Lin, Qi
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.05.2023
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Abstract In recent twenty years, aggregation-induced emission (AIE), due to its excellent application prospect, has aroused widespread interests. The development of novel and easy to make AIE luminogens (AIEgens) is an attractive subject. For this purpose, it is very important to study the structure-property relationship of AIEgens. Because azine derivatives are easy to synthesis and some of them have nice AIE properties, herein, a series of azine derivatives (ADs) were employed as models to study the influence of different functional groups, electronic effects and structures on the AIE properties of azine derivatives. The AIE mechanism were studied by single crystal analysis, density functional theory (DFT) calculations and so on. The results indicated that the o-hydroxyl aryl substituted azine compounds could show good AIE properties. Meanwhile, the AIE properties of o-hydroxyl aryl substituted azine compounds were also influenced by the electronic effects of the aryl groups in the azine compounds. The o-hydroxyl groups could form intramolecular hydrogen bond with imine group, which play key role to restrict the intramolecular rotation of the aryl groups and act as base stone for the AIE process of this kind compounds. The HOMO-LUMO energy gaps of o-hydroxyl substituted azine are smaller than other homologous compounds, which is agree with the proposed AIE mechanism. Finally, thanks to the AIE properties, the o-hydroxy-substituted azines could be used as efficient Al3+ and Cu2+ fluorescent chemosensors in different conditions. In addition, test strips based on AD10 has been prepared, which can conveniently detect Cu2+ in industrial wastewater. This research supplied a way for the design of novel easy to make AIEgens through simple azine derivatives. The AIE mechanism and structure-property relationship of azine derivatives were studied. The o-hydroxyl aryl substituted azine compounds could show good AIE properties and can act as Al3+ and Cu2+ sensor in different conditions. [Display omitted]
AbstractList In recent twenty years, aggregation-induced emission (AIE), due to its excellent application prospect, has aroused widespread interests. The development of novel and easy to make AIE luminogens (AIEgens) is an attractive subject. For this purpose, it is very important to study the structure-property relationship of AIEgens. Because azine derivatives are easy to synthesis and some of them have nice AIE properties, herein, a series of azine derivatives (ADs) were employed as models to study the influence of different functional groups, electronic effects and structures on the AIE properties of azine derivatives. The AIE mechanism were studied by single crystal analysis, density functional theory (DFT) calculations and so on. The results indicated that the o-hydroxyl aryl substituted azine compounds could show good AIE properties. Meanwhile, the AIE properties of o-hydroxyl aryl substituted azine compounds were also influenced by the electronic effects of the aryl groups in the azine compounds. The o-hydroxyl groups could form intramolecular hydrogen bond with imine group, which play key role to restrict the intramolecular rotation of the aryl groups and act as base stone for the AIE process of this kind compounds. The HOMO-LUMO energy gaps of o-hydroxyl substituted azine are smaller than other homologous compounds, which is agree with the proposed AIE mechanism. Finally, thanks to the AIE properties, the o-hydroxy-substituted azines could be used as efficient Al3+ and Cu2+ fluorescent chemosensors in different conditions. In addition, test strips based on AD10 has been prepared, which can conveniently detect Cu2+ in industrial wastewater. This research supplied a way for the design of novel easy to make AIEgens through simple azine derivatives. The AIE mechanism and structure-property relationship of azine derivatives were studied. The o-hydroxyl aryl substituted azine compounds could show good AIE properties and can act as Al3+ and Cu2+ sensor in different conditions. [Display omitted]
ArticleNumber 107792
Author Huang, Ting-Ting
Wei, Tai-Bao
Yao, Hong
Shi, Bingbing
Lin, Qi
Liu, Juan
Fu, Yong-Peng
Sun, Xiao-Mei
Tang, Zhong-Di
Li, Zhao-Hui
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  givenname: Juan
  surname: Liu
  fullname: Liu, Juan
  organization: Key Laboratory of Environment-Friendly Composite Materials of the State Ethnic Affairs Commission, College of Chemical Engineering, Northwest Minzu University, Lanzhou 730000 China
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  givenname: Zhao-Hui
  surname: Li
  fullname: Li, Zhao-Hui
  organization: Department of Pharmacy Jiangxi Medical College, Shangrao 334000, China
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  organization: Longnan Ecological and Environmental Monitoring Centre of Gansu Province, Longnan 746000, China
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  surname: Wei
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  email: linqi2004@126.com
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Issue 5
Keywords AIEgens
Structure-property relationship
Fluorescent chemosensor
Azine derivatives
Calculations
Language English
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Snippet In recent twenty years, aggregation-induced emission (AIE), due to its excellent application prospect, has aroused widespread interests. The development of...
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elsevier
SourceType Enrichment Source
Index Database
Publisher
StartPage 107792
SubjectTerms AIEgens
Azine derivatives
Calculations
Fluorescent chemosensor
Structure-property relationship
Title Structure-property relationship on aggregation-induced emission properties of simple azine-based AIEgens and its application in metal ions detection
URI https://dx.doi.org/10.1016/j.cclet.2022.107792
Volume 34
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