Synthesis, SC XRD based Structure Elucidation, Supramolecular Assembly Exploration Via Hirshfeld Surface Analysis, Computational and QTAIM Study of Functionalized Anilide

Authors

  • Muhammad Nawaz Tahir Department of Physics, University of Sargodha, 40100, Punjab, Pakistan
  • Muhammad Ashfaq Department of Physics, University of Sargodha, 40100, Punjab, Pakistan
  • Akbar Ali Department of Chemistry, Government College University, Faisalabad, Pakistan
  • Chin Hung Lai Department of Medical Applied Chemistry, Chung Shan Medical University, Taichung 40241, Taiwan Department of Medical Education, Chung Shan Medical University Hospital, Taichung 402, Taiwan
  • Bojja Rajeshwar Rao Senior Chemist (Retired), Chemical Division, Kakatiya Thermal Power Project (O&M) Chelpur-506 170, Telangana State, India
  • Irshad Ali Shahid Department of Physics, University of Sargodha, Sargodha 40100, Pakistan
  • Khurram Shahzad Munawar Department of Chemistry, University of Mianwali, 42200, Pakistan Department of Chemistry, University of Sargodha, 40100, Pakistan

DOI:

https://doi.org/10.17344/acsi.2023.8108

Keywords:

Crystal structure, Supramolecular assembly, Non-covalent interactions, Gas-phase DFT

Abstract

The anilide compound named (Z)-4-(2-methoxy-4-nitrophenyl)amino)-4-oxobut-2-enoic acid (MAOA) has been synthesized by the chemical reaction of 2-methoxy-4-nitroaniline and maleic anhydride in ethyl acetate. The synthesized compound was characterized by elemental analysis, FT-IR and UV-Vis spectroscopy, and TGA/DSC technique. Furthermore, the crystal structure was analyzed by the single crystal X-ray diffraction (SC XRD) technique. The supramolecular assembly of MAOA in terms of non-covalent interactions was explored by Hirshfeld surface analysis. Void analysis inferred that MAOA is expected to have good mechanical properties. The crystal packing environment was further investigated by interaction energy between molecular pairs and energy frameworks. Moreover, the result of the gas-phase DFT study showed that there is an intramolecular N–H···O and O–H···O hydrogen bond in MAOA due to the distance between D and A being smaller than the sum of their van der Waals radii. The result of the QTAIM study showed that there should also be an intramolecular CH···O hydrogen bond with a strength of 3.40 kcal/mol in MAOA.

Author Biography

Muhammad Ashfaq, Department of Physics, University of Sargodha, 40100, Punjab, Pakistan

Lecturer in Department of Physics, University of Sargodha. I am working in single crystal XRD lab in university.

Published

31.05.2023

Issue

Section

Organic chemistry