Issue 73, 2018

Molecular design and synthesis of new dithiocarbazate complexes; crystal structure, bioactivities and nano studies

Abstract

The syntheses of a new set of metal complexes MoO2L′(CH3OH), VOL′(CH3O)(CH3OH), Image ID:c8ra07100d-t1.gif, Image ID:c8ra07100d-t2.gif, SnL′Cl2 and SnL′I2 with a new ligand (L = (2,2′(disulfanediylbis((ethylthio)methylene)bis(hydrazin-2-yl-1-ylidene)bis(methanylylidene)) diphenol; L′ = S-ethyl-3-(2-hydroxyphenyl)methylenedithiocarbazate are described along with characterization by elemental analysis, mass spectrometry, spectroscopic (IR, 1H- and 13C-NMR) and TGA techniques. The crystal structures of compounds were determined by single crystal X-ray diffraction analysis and compared to powder X-ray diffraction (PXRD) patterns of the nano complexes obtained using ultrasonic methods. The PXRD results indicate that the compounds synthesized by ultrasonic methods have high crystallinity. The compounds were evaluated in an in vitro cytotoxicity study with two human cancer cell lines. The results of this study revealed that all complexes exhibit good cytotoxic activity when compared to the clinical drug, cisplatin. Interaction of the samples with human serum albumin (HSA) was investigated using fluorescence spectrophotometric methods and the Stern–Volmer quenching constant (KSV) and free energy changes (ΔG) were calculated at 298 K. The fluorescence quenching method is used to determine the number of binding sites (n) and association constants (Ka) at the same temperatures.

Graphical abstract: Molecular design and synthesis of new dithiocarbazate complexes; crystal structure, bioactivities and nano studies

Supplementary files

Article information

Article type
Paper
Submitted
25 Aug 2018
Accepted
24 Sep 2018
First published
14 Dec 2018
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2018,8, 41795-41809

Molecular design and synthesis of new dithiocarbazate complexes; crystal structure, bioactivities and nano studies

Z. Yekke-ghasemi, R. Takjoo, M. Ramezani and J. T. Mague, RSC Adv., 2018, 8, 41795 DOI: 10.1039/C8RA07100D

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