Synthesis, Characterization and Solvatochromic Studies Using the Solvent Polarity Parameter, ENT on 2-Chloro-3-Ethylamino-1,4-Naphthoquinone

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 H 1 -...

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Veröffentlicht in:Journal of fluorescence 2017-07, Vol.27 (4), p.1505-1512
Hauptverfasser: Durairaj, Arulappan, Obadiah, Asir, Ramanathan, Subramanian, Johnson, Princy Merlin, Bella, Antony Paulraj, Vasanthkumar, Samuel
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Sprache:eng
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Zusammenfassung: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 H 1 -NMR, C 13 -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 (μ g ) and excited state (μ e ) dipole moments were calculated. The angle between the excited state and ground state dipole moments were also calculated. Graphical Abstract ᅟ
ISSN:1053-0509
1573-4994
DOI:10.1007/s10895-017-2090-6