Synthesis and photophysical studies of new fluorescent naphthalene chalcone

This study reports the base-catalyzed Aldol condensation route for synthesizing a new naphthalene chalcone derivative (C1). The molecular structure of C1 was ascertained by FTIR, NMR (<sup>1</sup>H and <sup>13</sup>C NMR) spectroscopy, and mass spectrometry. Optical properties were explored through UV-Visible absorption and photoluminescence spectroscopy. The UV-Vis spectrum indicated the presence of absorption bands from 300 to 350 nm due to π-π* transitions. In the solid state, C1 had a broad excitation that resulted in a solitary emission peak, whereas in solution, it emitted fluorescence at 495 nm. Density Functional Theory (DFT) calculations were carried out to investigate the electronic configuration and optical properties further. These findings suggest that the synthesized compound may possess favorable properties in optoelectronic and sensing applications.

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Publication Details

Journal
Scientific Reports
Published
2025-08-28
DOI
https://doi.org/10.1038/s41598-025-17566-1
Citations
2
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
1.87
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article

Synthesis and photophysical studies of new fluorescent naphthalene chalcone

Rajeev K. Sinha, Nitinkumar S. Shetty, Maruthi Nagavalli Yogeesh, C. H. Raksha
2 citations
Scientific Reports
Synthesis and biological activity
1.87
article

Synthesis and photophysical studies of new fluorescent naphthalene chalcone

Rajeev K. Sinha, Nitinkumar S. Shetty, Maruthi Nagavalli Yogeesh, C. H. Raksha
article en
2 citations

Abstract

This study reports the base-catalyzed Aldol condensation route for synthesizing a new naphthalene chalcone derivative (C1). The molecular structure of C1 was ascertained by FTIR, NMR (<sup>1</sup>H and <sup>13</sup>C NMR) spectroscopy, and mass spectrometry. Optical properties were explored through UV-Visible absorption and photoluminescence spectroscopy. The UV-Vis spectrum indicated the presence of absorption bands from 300 to 350 nm due to π-π* transitions. In the solid state, C1 had a broad excitation that resulted in a solitary emission peak, whereas in solution, it emitted fluorescence at 495 nm. Density Functional Theory (DFT) calculations were carried out to investigate the electronic configuration and optical properties further. These findings suggest that the synthesized compound may possess favorable properties in optoelectronic and sensing applications.

Scientific ReportsVol. 15(1)
Birla Institute of Technology, Mesra (IN), Manipal Academy of Higher Education (IN)
Openalex Percentile: Top 14%
Synthesis and biological activity
1.87
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