| Literature DB >> 28405932 |
Arulappan Durairaj1, Asir Obadiah1, Subramanian Ramanathan1, Princy Merlin Johnson2, Antony Paulraj Bella2, Samuel Vasanthkumar3.
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. Graphical Abstract ᅟ.Entities:
Keywords: 2-chloro-3-ethylamino-1,4-naphthoquinone; Dipole moments; Kawski-Chamma-Viallet, Reichardt equations; Lippert-Mataga, Bakshiev’s
Year: 2017 PMID: 28405932 DOI: 10.1007/s10895-017-2090-6
Source DB: PubMed Journal: J Fluoresc ISSN: 1053-0509 Impact factor: 2.217