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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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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 |
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author | 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. |
author_facet | 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. |
author_sort | Rajendran, Satheeshkumar |
collection | PubMed |
description | [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. |
format | Online Article Text |
id | pubmed-10666135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106661352023-11-08 Enhanced Method for the Synthesis and Comprehensive Characterization of 1-(4-Phenylquinolin-2-yl)propan-1-one 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. ACS Omega [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. American Chemical Society 2023-11-08 /pmc/articles/PMC10666135/ /pubmed/38027353 http://dx.doi.org/10.1021/acsomega.3c04360 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | 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. Enhanced Method for the Synthesis and Comprehensive Characterization of 1-(4-Phenylquinolin-2-yl)propan-1-one |
title | Enhanced Method
for the Synthesis and Comprehensive
Characterization of 1-(4-Phenylquinolin-2-yl)propan-1-one |
title_full | Enhanced Method
for the Synthesis and Comprehensive
Characterization of 1-(4-Phenylquinolin-2-yl)propan-1-one |
title_fullStr | Enhanced Method
for the Synthesis and Comprehensive
Characterization of 1-(4-Phenylquinolin-2-yl)propan-1-one |
title_full_unstemmed | Enhanced Method
for the Synthesis and Comprehensive
Characterization of 1-(4-Phenylquinolin-2-yl)propan-1-one |
title_short | Enhanced Method
for the Synthesis and Comprehensive
Characterization of 1-(4-Phenylquinolin-2-yl)propan-1-one |
title_sort | enhanced method
for the synthesis and comprehensive
characterization of 1-(4-phenylquinolin-2-yl)propan-1-one |
url | 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 |
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