A Comprehensive Study of Pharmacologic Complexity: Study of Interactions and Properties of Paracetamol, Aspirin, Naproxen, and Diclofenac

The present study explores the molecular and electronic properties of four widely used pharmaceutical compounds—Paracetamol, Aspirin, Naproxen, and Diclofenac—to enhance our understanding of their stability, reactivity, and potential applications in drug design. Through computational analysis, key electronic properties and intermolecular interactions were examined to reveal factors influencing their chemical behavior. Using density functional theory (DFT) with the B3LYP/6-31G(d,p) level, the study investigates their electronic structure, charge distribution, and optical characteristics. Reduced Density Gradient (RDG) and Non-Covalent Interaction (NCI) analyses highlight distinct intermolecular interactions, such as strong hydrogen bonding in Paracetamol, π→π* transition stabilization in Aspirin, dispersion interactions in Naproxen, and diverse attractive forces in Diclofenac. Natural Bond Orbital (NBO) analysis further elucidates electron delocalization effects. The study also evaluates Nonlinear Optical (NLO) properties, suggesting potential applications beyond pharmaceuticals. Quantum chemical parameters indicate that Aspirin has the highest ionization energy (10.18 eV), making it a strong electron acceptor, while Paracetamol demonstrates significant electron-donating ability. Molecular Electrostatic Potential (MEP) mapping provides insights into charge distribution and reactivity, while UV-Visible absorption spectra reveal optical characteristics relevant to various applications. These findings offer valuable insights into the fundamental electronic behavior of these pharmaceutical compounds, which may inform drug formulation, bioavailability studies, and potential modifications for enhanced therapeutic efficacy. By linking computational analysis with pharmaceutical applications, this study contributes to a deeper understanding of molecular interactions that govern drug stability and performance.

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Publication Details

Journal
Orbital - The Electronic Journal of Chemistry
Published
2025-04-27
DOI
https://doi.org/10.17807/orbital.v17i1.19889
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
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article

A Comprehensive Study of Pharmacologic Complexity: Study of Interactions and Properties of Paracetamol, Aspirin, Naproxen, and Diclofenac

Rebaz Anwar Omer, Aryan Fathulla Qader, Yousif Hussein Azeez, Karzan A. Omar et al.
Orbital - The Electronic Journal of Chemistry
Analytical Methods in Pharmaceuticals
article

A Comprehensive Study of Pharmacologic Complexity: Study of Interactions and Properties of Paracetamol, Aspirin, Naproxen, and Diclofenac

Rebaz Anwar Omer, Aryan Fathulla Qader, Yousif Hussein Azeez, Karzan A. Omar, Khdir Ahmed Othman
article en

Abstract

The present study explores the molecular and electronic properties of four widely used pharmaceutical compounds—Paracetamol, Aspirin, Naproxen, and Diclofenac—to enhance our understanding of their stability, reactivity, and potential applications in drug design. Through computational analysis, key electronic properties and intermolecular interactions were examined to reveal factors influencing their chemical behavior. Using density functional theory (DFT) with the B3LYP/6-31G(d,p) level, the study investigates their electronic structure, charge distribution, and optical characteristics. Reduced Density Gradient (RDG) and Non-Covalent Interaction (NCI) analyses highlight distinct intermolecular interactions, such as strong hydrogen bonding in Paracetamol, π→π* transition stabilization in Aspirin, dispersion interactions in Naproxen, and diverse attractive forces in Diclofenac. Natural Bond Orbital (NBO) analysis further elucidates electron delocalization effects. The study also evaluates Nonlinear Optical (NLO) properties, suggesting potential applications beyond pharmaceuticals. Quantum chemical parameters indicate that Aspirin has the highest ionization energy (10.18 eV), making it a strong electron acceptor, while Paracetamol demonstrates significant electron-donating ability. Molecular Electrostatic Potential (MEP) mapping provides insights into charge distribution and reactivity, while UV-Visible absorption spectra reveal optical characteristics relevant to various applications. These findings offer valuable insights into the fundamental electronic behavior of these pharmaceutical compounds, which may inform drug formulation, bioavailability studies, and potential modifications for enhanced therapeutic efficacy. By linking computational analysis with pharmaceutical applications, this study contributes to a deeper understanding of molecular interactions that govern drug stability and performance.

Orbital - The Electronic Journal of Chemistry
University of Halabja (IQ), Koya University (IQ)
Openalex Percentile: Top 89%
Analytical Methods in Pharmaceuticals
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