Synthesis, Structural, and Intriguing Electronic Properties of Symmetrical Bis-Aryl-α,β-Unsaturated Ketone Derivatives
Akbar Ali, Muhammad Ashfaq, Zia Ud Din, Muhammad Ibrahim, Muhammad Khalid, Mohammed A. Assiri, Arish Riaz, Muhammad Nawaz Tahir, Edson Rodrigues‐Filho, Muhammad Imran, Aleksey E. Kuznetsov
Abstract
are relatively stable in redox processes and have high thermodynamic stability and relatively lower reactivity in general. The molecular electrostatic potential (MEP) analysis results imply potential formation of the intermolecular hydrogen bonding and dispersion interactions, which stabilizes the crystal structures of these compounds.
Topics & Concepts
ChemistryNatural bond orbitalCrystallographyCrystal structureArylDensity functional theoryMoleculeComputational chemistryOrganic chemistryAlkylStructural and Chemical Analysis of Organic and Inorganic CompoundsSynthesis of heterocyclic compoundsCrystal structures of chemical compounds