Abstract
Quinones are molecules with varied biological activities and electronic properties which are used for important applications [1, 2]. Quinone with a heteroatom substituted, namely 2-chloro-3-ethylamino-1,4-naphthoquinone (N-CAN) was synthesized and characterized by various techniques such as H1-NMR, C13-NMR, Mass spectroscopy and FT-IR spectroscopy. In this study, the solvatochromic effects on the spectral properties of 2-chloro-3-ethylamino-1,4-naphthoquinone have been investigated in different solvents taking into consideration, the solvent parameters like dielectric constant (ε) and refractive index (η) of different solvent polarities. Using Lippert-Mataga, Bakshiev’s, Kawski-Chamma-Viallet and Reichardt equations, the ground state (μg) and excited state (μe) dipole moments were calculated. The angle between the excited state and ground state dipole moments were also calculated.
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The authors thank the Management and the authorities of Karunya University, Coimbatore, for their kind support, constant encouragement.
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Durairaj, A., Obadiah, A., Ramanathan, S. et al. Synthesis, Characterization and Solvatochromic Studies Using the Solvent Polarity Parameter, ENT on 2-Chloro-3-Ethylamino-1,4-Naphthoquinone. J Fluoresc 27, 1505–1512 (2017). https://doi.org/10.1007/s10895-017-2090-6
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DOI: https://doi.org/10.1007/s10895-017-2090-6