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Synthesis, structural, spectral characterization and in vitro biological evaluation of ammonium trans-1, 2-cyclohexanediaminetetraacetato copper(II) dihydrate

K. Naresh, A. Mani, B. Archana, B. Preethi, B. N. Sivasankar, and C. Sivakumar

Department of Science and Humanities (Chemistry), Dhanalakshmi Srinivasan College of Engineering, Coimbatore, India

 

E-mail: nareshkrish9230@gmail.com

Received: 17 April 2025  Accepted: 22 August 2025

Abstract:

A novel ammonium trans-1,2-cyclohexanediaminetetraacetato copper(II) dihydrate complex, NH4[Cu(Hcdta)]·2H2O, was synthesized and thoroughly characterized by elemental analysis, FT-IR, electronic spectroscopy, thermal analysis, and single-crystal X-ray diffraction. The complex features a five-coordinate distorted square pyramidal geometry around the Cu(II) center, coordinated by two nitrogen and three oxygen atoms, with one carboxymethyl group uncoordinated. Its structure is further stabilized by extensive hydrogen bonding network involving coordinated and lattice water molecules, confirmed through Hirshfeld surface analysis. Spectroscopic data revealed characteristic d–d and ligand-to-metal charge transfer transitions, while thermal studies showed stepwise dehydration, ammonia loss, and final decomposition to Cu2O. Biological investigations demonstrated strong intercalative binding with calf thymus DNA, supported by UV–Vis spectral hypochromism, red shifts, and fluorescence enhancement. The complex exhibited moderate antibacterial and potent antifungal activity comparable to standard drugs, alongside selective cytotoxicity against human lung (A549), breast (MCF-7), and cervical (HeLa) cancer cell lines, with minimal toxicity toward normal keratinocytes. These results highlight NH4[Cu(Hcdta)]·2H2O as a promising multifunctional agent for antibacterial and anticancer applications, highlighting the impact of the cyclohexane backbone in CDTA on metal coordination and biological function.

Keywords: Square pyramidal geometry; Hirshfeld surface analysis; Crystal structure; DNA binding; Antimicrobial activity

Full paper is available at www.springerlink.com.

DOI: 10.1007/s11696-025-04447-0

 

Chemical Papers 80 (2) 1223–1240 (2026)

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