Photophysical Properties and Metal‐Free Synthesis of Thiophene‐Based D─π─A Stilbenes with Enhanced Stokes Shift

Abstract A straightforward and practical nucleophile‐induced synthetic route for the synthesis of thermally stable, fluorescently active, functionalized stilbenes has been developed. The described synthetic method involves nucleophile‐induced, base‐promoted ring transformation reactions following a more traditional approach. All reactions occur at room temperature, yielding high amounts of the desired product with minimal byproducts. Due to the inclusion of a donor‐π‐acceptor system, all the produced stilbenes exhibited impressive emission characteristics. The resulting band gaps ranged from 3.37 to 3.93 eV, indicating a notable redshift. Solvatochromic investigations underscored these positive impacts. Furthermore, the TG‐DTA analysis indicated a single‐step evaporation process, and the compounds exhibited stability up to 375 °C.

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Publication Details

Journal
ChemistrySelect
Published
2024-11-29
DOI
https://doi.org/10.1002/slct.202403407
Citations
6
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
Field-Weighted Citation Impact
0.70
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article

Photophysical Properties and Metal‐Free Synthesis of Thiophene‐Based D─π─A Stilbenes with Enhanced Stokes Shift

Kokila Sakthivel, Fateh V. Singh
6 citations
ChemistrySelect
Porphyrin and Phthalocyanine Chemistry
0.70
article

Photophysical Properties and Metal‐Free Synthesis of Thiophene‐Based D─π─A Stilbenes with Enhanced Stokes Shift

Kokila Sakthivel, Fateh V. Singh
article en
6 citations

Abstract

Abstract A straightforward and practical nucleophile‐induced synthetic route for the synthesis of thermally stable, fluorescently active, functionalized stilbenes has been developed. The described synthetic method involves nucleophile‐induced, base‐promoted ring transformation reactions following a more traditional approach. All reactions occur at room temperature, yielding high amounts of the desired product with minimal byproducts. Due to the inclusion of a donor‐π‐acceptor system, all the produced stilbenes exhibited impressive emission characteristics. The resulting band gaps ranged from 3.37 to 3.93 eV, indicating a notable redshift. Solvatochromic investigations underscored these positive impacts. Furthermore, the TG‐DTA analysis indicated a single‐step evaporation process, and the compounds exhibited stability up to 375 °C.

ChemistrySelectVol. 9(45)
Vellore Institute of Technology University (IN)
Clean water and sanitation
Openalex Percentile: Top 29%
Porphyrin and Phthalocyanine Chemistry
0.70
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