Unveiling the aggregation-induced chromic emission of triazine anchored BODIPYs

被引：0

作者：

Satardekar, Pranay ^{[1
]}

Chaudhari, Vaishali ^{[2
]}

Siddiqui, Zahir Ali ^{[1
,3
]}

Lambud, Sushil ^{[1
]}

Sekar, Nagaiyan ^{[3
]}

Bhosale, Rajesh ^{[4
]}

More, Sandeep ^{[1
]}

机构：

[1] Inst Chem Technol, Dept Fibres & Text Proc Technol, Mumbai 400019, Maharashtra, India

[2] Indrashil Univ, Sch Sci, Dept Chem, Mehsana 382470, Gujarat, India

[3] Inst Chem Technol, Dept Special Chem Technol, Mumbai 400019, Maharashtra, India

[4] Ganpat Univ, Ctr Adv Res Studies, Mehsana 384012, Gujarat, India

来源：

NEW JOURNAL OF CHEMISTRY | 2024年 / 48卷 / 39期

关键词：

DENSITY-FUNCTIONAL THERMOCHEMISTRY; INTRAMOLECULAR CHARGE-TRANSFER; FLUORESCENCE; DYES; RED; DERIVATIVES; SUBSTITUENTS; CHEMISTRY; BEHAVIOR; PROBES;

D O I：

10.1039/d4nj03757j

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

BODIPY derivatives based on 2,4,6-trichloro-1,3,5-triazine have been successfully synthesized and characterized. These molecular systems demonstrate restricted intramolecular rotation (RIR) and J-aggregation, leading to aggregation-induced chromic emission (AICE), with notable green-red fluorescence color switching. Additionally, these derivatives exhibit distinctive self-assembly behaviour and solid-state emission properties. These findings showcase their potential for diverse applications across multiple fields. Triazine-based BODIPY dyes exhibiting restricted intramolecular rotation and J-aggregation, leading to aggregation-induced chromic emission (AICE) with green-to-red emission color switching and self-assembly behaviour in the aggregated state.

引用

页码：17215 / 17225

页数：11

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