Publication Type Journal Article
Title Copper(II) complexes of functionalized 2,2 :6 ,2 -terpyridines and 2,6-di(thiazol-2-yl)pyridine: structure, spectroscopy, cytotoxicity and catalytic activity
Authors Katarzyna Czerwinska Barbara Machura Slawomir Kula Stanislaw Krompiec Karol Erfurt Catarina Roma-Rodrigues A.R. Fernandes Lidia S. Shul?pina Nikolay S. Ikonnikov Georgiy B. Shul'pin
Groups
Journal DALTON TRANSACTIONS
Year 2017
Month August
Volume 46
Number 29
Pages 9591-9604
Abstract Six new copper(II) complexes with 2,2 :6 ,2 -terpyridine (4 -R-n-terpy) [1 (R-1 = furan-2-yl), 2 (R-2 = thiophen-2-yl), and 3 (R-3 = 1-methyl-1H-pyrrol-2-yl)] and 2,6-di(thiazol-2-yl) pyridine derivatives (R-n-dtpy) [4 (R-1), 5 (R-2), and 6 (R-3)] have been synthesized by a reaction between copper(II) chloride and the corresponding ligand. The complexes have been characterized by UV-vis and IR spectroscopy, and their structures have been determined by X-ray analysis. The antiproliferative potential of copper(II) complexes of 2,2 : 6 , 2 -terpyridine and 2,6-di(thiazol-2-yl) pyridine derivatives towards human colorectal (HCT116) and ovarian (A2780) carcinoma as well as towards lung (A549) and breast adenocarcinoma (MCF7) cell lines was examined. Complex 1 and complex 6 were found to have the highest antiproliferative effect on A2780 ovarian carcinoma cells, particularly when compared with complex 2, 3 with no antiproliferative effect. The order of cytotoxicity in this cell line is 6 > 1 > 5 > 4 > 2 approximate to 3. Complex 2 seems to be much more specific towards colorectal carcinoma HCT116 and lung adenocarcinoma A549 cells. The viability loss induced by the complexes agrees with Hoechst 33258 staining and typical morphological apoptotic characteristics like chromatin condensation and nuclear fragmentation. The specificity towards different types of cell lines and the low cytotoxic activity towards healthy cells are of particular interest and are a positive feature for further developments. Complexes 1-6 were also tested in the oxidation of alkanes and alcohols with hydrogen peroxide and tert-butyl-hydroperoxide (TBHP). The most active catalyst 4 gave, after 120 min, 0.105 M of cyclohexanol + cyclohexanone after reduction with PPh3. This concentration corresponds to a yield of 23\% and TON = 210. Oxidation of cis-1,2-dimethylcyclohexane with m-CPBA catalyzed by 4 in the presence of HNO3 gave a product of a stereoselective reaction (trans/cis = 0.47). Oxidation of secondary alcohols afforded the target ketones in yields up to 98\% and TON = 630.
DOI http://dx.doi.org/10.1039/c7dt01244f
ISBN
Publisher
Book Title
ISSN 1477-9226
EISSN 1477-9234
Conference Name
Bibtex ID ISI:000408692700032
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