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 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
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.
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ISSN: | 1053-0509 1573-4994 |
DOI: | 10.1007/s10895-017-2090-6 |