Influence of Aliphatic Substituents on the Properties of 2,1,3-Benzothiadiazole-Based Luminophores

In this work, a series of 2,1,3-benzothiadiazole (BTD)-based organic luminophores which include 2,5-thiophene and 1,4-benzene moieties and terminal alkyl chains in their structures were synthesized. The effect of the length of the alkyl chain on the solubility, optical and thermal properties of the resulting luminophores was investigated. The introduction of alkyl substituents leads to a slight bathochromic shift of the absorption and luminescence maxima compared to their unsubstituted analog. As the length of the aliphatic chain increases, the melting point of the BTD-based luminophores decreases. The length of the aliphatic chain strongly affects the solubility of the molecules obtained.

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Publication Details

Journal
INEOS OPEN
Published
2025-04-29
DOI
https://doi.org/10.32931/io2536a
Primary Topic
Synthesis and biological activity
Type
article
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article

Influence of Aliphatic Substituents on the Properties of 2,1,3-Benzothiadiazole-Based Luminophores

Sergey A. Ponomarenko, Evgeniya A. Svidchenko, Oleg V. Borshchev, В. В. Попова et al.
INEOS OPEN
Synthesis and biological activity
article

Influence of Aliphatic Substituents on the Properties of 2,1,3-Benzothiadiazole-Based Luminophores

Sergey A. Ponomarenko, Evgeniya A. Svidchenko, Oleg V. Borshchev, В. В. Попова, D. E. Stakanova
article en

Abstract

In this work, a series of 2,1,3-benzothiadiazole (BTD)-based organic luminophores which include 2,5-thiophene and 1,4-benzene moieties and terminal alkyl chains in their structures were synthesized. The effect of the length of the alkyl chain on the solubility, optical and thermal properties of the resulting luminophores was investigated. The introduction of alkyl substituents leads to a slight bathochromic shift of the absorption and luminescence maxima compared to their unsubstituted analog. As the length of the aliphatic chain increases, the melting point of the BTD-based luminophores decreases. The length of the aliphatic chain strongly affects the solubility of the molecules obtained.

INEOS OPENVol. 8(1-3)
Openalex Percentile: Top 84%
Synthesis and biological activity
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