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.
Authors
- Kokila Sakthivel
- Fateh V. Singh (ORCID: https://orcid.org/0000-0002-6358-4408)
Institutions
- Vellore Institute of Technology University (IN)
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