Theoretical Study of Copper(II) Coordination Complexes with Coumarin-Derived Heterocyclic Ligands Through DFT and CDFT

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Authors: Jesús Baldenebro-López, Rody Soto-Rojo, Daniel Glossman-Mitnik
Cited by: 4
References: 42

Abstract

Copper(II) coordination complexes with coumarin-derived heterocyclic ligands are promising in inorganic therapeutics for anticancer and antimicrobial applications. To establish quantitative structure–activity relationships for lead design, we studied six copper(II) complexes (Cu1–Cu6)with four- and five-coordinate geometries using Density Functional Theory, Conceptual Density Functional Theory, and visualization analyses. Geometry optimization at M06/6-31G(d)+DZVP revealed distorted coordination environments from d9 Jahn–Teller effects. Tridentate N2O-chelatedcomplexes (Cu4–Cu6) showed greater aqueous stability (ΔGsolv=−43 to −50 kcal·mol−1) than four-coordinate analogs (−29 to −31 kcal·mol−1). CDFT global descriptors contrasted reactivity: four-coordinate Cu1–Cu2 had higher electron affinity (>4.2 eV) and electrophilicity (>5.7 eV), suggesting propensity for redox cycling and for undergoing nucleophilic attack by DNA bases, whereas Cu4–Cu6 displayed increased chemical hardness (3.43–3.54 eV) and lower electrophilicity (≈3.8 eV), implying enhanced kinetic stability and bioavailability. Frontier orbital analysis indicated ligand-to-metal charge transfer via a LUMO delocalized over the π-conjugated coumarin, facilitating intercalation by π-π stacking. The visualization showed strong covalent bonds (blue isosurfaces) stabilizing the metal and dispersive π interactions (green surfaces) on the ligand, enabling solvent interactions and biomolecular recognition. Tridentate N2O coordination thus balances electronic stability and biological reactivity, making Cu4–Cu6 promising for further study.

Fields of Study & Subjects

Metal complexes synthesis and properties Metal-Organic Frameworks: Synthesis and Applications Cancer Research and Treatment

Publication details

Journal / source
Processes
Publisher
MDPI AG
Volume
14
Issue
3
Pages
498–498
Publication date
31 January 2026
Language
EN