Issue 1, 2018

Cyclometallated ruthenium(ii) complexes with 3-acetyl-2[H]-chromene-2-one derived CNS chelating ligand systems: synthesis, X-ray characterization and biological evaluation

Abstract

Four new bivalent organoruthenium complexes incorporated with 3-acetylcoumarin-4(N)-substituted thiosemicarbazones were synthesized. Comprehensive spectral and analytical techniques such as elemental analyses, IR, UV-vis, 1H NMR and 13C NMR provided proof of the formation of the complexes (1–4). Single crystals obtained for two ligands and the four complexes were characterized by X-ray crystallographic studies, which indicated CNS tridentate coordination of the ligands through C–H activation at the C(4) carbon of the pyrone ring of coumarin. The ligands and complexes intercalated with calf thymus DNA (CT DNA), supported by EB displacement studies and DNA viscosity measurements. The compounds bound well with two serum albumins (bovine serum albumin (BSA) and human serum albumin (HSA)) and the quenching mechanism was found to be static. Antioxidant studies revealed the radical scavenging proficiency of the compounds. The compounds showed better antimicrobial activity against two Gram-positive bacteria (Staphylococcus aureus and Streptococcus pneumonie), two Gram-negative bacteria (Pseudomonas aeruginosa and Salmonella paratyphi) and five fungi (Candida albicans, Trichophyton rubrum, Aspergillus niger, Aspergillus fumigates and Candida tropicalis). The in vitro cytotoxic abilities of the compounds were analysed using the MTT assay on MCF-7 (human breast cancer) and A549 (human lung carcinoma) cell lines and compared with standard cisplatin. Activities greater than cisplatin were observed for the ligands as well as the complexes. Assays on the human normal keratinocyte cell line HaCaT showed that the compounds were non-toxic to those cells. In all the biological studies done, the complexes displayed better activity than the ligands and among them, complex 3 stood out as the best, owing to the greater electron donating ability of the N-terminal ethyl group on the thiosemicarbazone. The results implied that N-terminal substitution played a significant role in bringing out the bioactivity of the complexes.

Graphical abstract: Cyclometallated ruthenium(ii) complexes with 3-acetyl-2[H]-chromene-2-one derived CNS chelating ligand systems: synthesis, X-ray characterization and biological evaluation

Supplementary files

Article information

Article type
Paper
Submitted
04 Aug 2017
Accepted
14 Nov 2017
First published
30 Nov 2017

New J. Chem., 2018,42, 336-354

Cyclometallated ruthenium(II) complexes with 3-acetyl-2[H]-chromene-2-one derived CNS chelating ligand systems: synthesis, X-ray characterization and biological evaluation

G. Kalaiarasi, S. R. J. Rajkumar, S. Dharani, F. R. Fronczek, M. S. A. Muthukumar Nadar and R. Prabhakaran, New J. Chem., 2018, 42, 336 DOI: 10.1039/C7NJ02877F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements