Synthesis and fluorescence studies of selected N-aryl-2-aminoquinolines: Effect of hydrogen bonding, substituents and ESIPT on their fluorescence quantum yields
Document Type
Article
Publication Date
1-1-2019
Abstract
N-aryl-2-aminoquinolines have been widely synthesised and used in biological applications. However, their luminescence properties have not been studied in detail. Herein a series of N-aryl-2-aminoquinolines was synthesised from substitution reaction between 2-chloroquinoline and anilines with different substituent groups gave sufficient yield from 72–90%. The fluorescence behaviour was investigated in toluene, ethyl acetate and ethanol. The result shows that fluorescence quantum yield of N-aryl-2-aminoquinolines was the highest in toluene, followed by in ethyl acetate and the lowest in ethanol. Quenched emission observed in ethanol is caused by site-specific fluorophore-solvent hydrogen bonding interactions, inducing deactivation of the quinolinyl ring system. The bell-shaped Hammett plot of various substituted compounds suggested that both strong electron donating and electron withdrawing groups caused significant quenching in the fluorescence quantum yields. Therefore, most types of substituent groups on the phenyl moiety, hydrogen bonding between the fluorophore and solvent, and excited-state intramolecular proton transfer (ESIPT) were found as crucial contributors to fluorescence quenching of N-aryl-2-aminoquinolines.
Keywords
N-aryl-2-aminoquinolines, Fluorescence quenching, Hydrogen bonding, Substituent effects, ESIPT
Divisions
CHEMISTRY
Funders
Ministry of Higher Education (MOHE), Malaysia under research grant scheme MO002-2014,University of Malaya Research Grant (UMRG) Schemes RP002B-13BIO and RG340-15AFR
Publication Title
Journal of Luminescence
Volume
208
Publisher
Elsevier