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Enhanced Method for the Synthesis and Comprehensive Characterization of 1-(4-Phenylquinolin-2-yl)propan-1-one

[Image: see text] We present an enhanced method for synthesizing a novel compound, 1-(4-phenylquinolin-2-yl)propan-1-one (3), through the solvent-free Friedländer quinoline synthesis using poly(phosphoric acid) as an assisting agent. The crystal structure of compound 3 is analyzed using FT-IR, and t...

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Detalles Bibliográficos
Autores principales: Rajendran, Satheeshkumar, Montecinos, Rodrigo, Cisterna, Jonathan, Prabha, Kolandaivel, Rajendra Prasad, Karnam Jayarampillai, Palakurthi, Sushesh Srivatsa, Aljabali, Alaa A. A, Naikoo, Gowhar A., Mishra, Vijay, Acevedo, Roberto, Sayin, Koray, Charbe, Nitin Bharat, Tambuwala, Murtaza M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666135/
https://www.ncbi.nlm.nih.gov/pubmed/38027353
http://dx.doi.org/10.1021/acsomega.3c04360
Descripción
Sumario:[Image: see text] We present an enhanced method for synthesizing a novel compound, 1-(4-phenylquinolin-2-yl)propan-1-one (3), through the solvent-free Friedländer quinoline synthesis using poly(phosphoric acid) as an assisting agent. The crystal structure of compound 3 is analyzed using FT-IR, and the chemical shifts of its (1)H- and (13)C NMR spectra are measured and calculated using B3LYP/6-311G(d,p), CAM-B3LYP/6-311G(d,p), and M06-2X/6-311G(d,p) basis sets in the gas phase. Additionally, the optimized geometry of quinoline 3 is compared with experimental X-ray diffraction values. Through density functional theory calculations, we explore various aspects of the compound’s properties, including noncovalent interactions, Hirshfeld surface analysis, nonlinear optical properties, thermodynamic properties, molecular electrostatic potential, and frontier molecular orbitals. These investigations reveal chemically active sites within this quinoline derivative that contribute to its chemical reactivity.