People | Locations | Statistics |
---|---|---|
Naji, M. |
| |
Motta, Antonella |
| |
Aletan, Dirar |
| |
Mohamed, Tarek |
| |
Ertürk, Emre |
| |
Taccardi, Nicola |
| |
Kononenko, Denys |
| |
Petrov, R. H. | Madrid |
|
Alshaaer, Mazen | Brussels |
|
Bih, L. |
| |
Casati, R. |
| |
Muller, Hermance |
| |
Kočí, Jan | Prague |
|
Šuljagić, Marija |
| |
Kalteremidou, Kalliopi-Artemi | Brussels |
|
Azam, Siraj |
| |
Ospanova, Alyiya |
| |
Blanpain, Bart |
| |
Ali, M. A. |
| |
Popa, V. |
| |
Rančić, M. |
| |
Ollier, Nadège |
| |
Azevedo, Nuno Monteiro |
| |
Landes, Michael |
| |
Rignanese, Gian-Marco |
|
Bagchi, Arka
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (1/1 displayed)
Places of action
Organizations | Location | People |
---|
article
Synthesis, spectroscopy and structural elucidation of two new CoII and NiII complexes of pyrazole derived heterocyclic Schiff base ligand as potential anticancer and photocatalytic agents
Abstract
Two new complexes I and II of general composition, [ML<sub>3</sub>]X<sub>2</sub>.nH<sub>2</sub>O (where, M = Co<sup style="box-sizing: inherit; color: rgb(34, 34, 34); font-family: Merriweather, serif;">II</sup> and Ni<sup style="box-sizing: inherit; color: rgb(34, 34, 34); font-family: Merriweather, serif;">II</sup> for I and II, respectively, L = MPAFA, X = Br and n = 2) were synthesized from a pyrazolyl Schiff base ligand, MPAFA (L). I and II were characterised through several physico-chemical and spectroscopic techniques, viz., C, H, N analyses, estimation of metal contents, conductance and magnetic susceptibility measurements, IR, electronic and fluorescence spectral studies. Both the reported coordination complexes were cationic in nature and behaved as 1:2 electrolytes. According to IR spectra, each of the MPAFA molecule coordinated to the metal centres via the azomethine nitrogen and the pyrazolyl tertiary nitrogen atoms. Single crystal X-ray diffraction studies of I and II had established a N6 donor set with a distorted octahedral structure for both the cases. Both the complexes exhibited some non-covalent interactions, like π…π stacking, H-bonding contacts etc. L, I and II had also been found to possess fluorescence property. Anticancer activities of L, I and II had been investigated and it was found that both the complexes I and II were stronger cytotoxic agents against the breast cancer cell line MCF7 than the primary ligand system; while all of them (L, I and II) were less toxic against a non-cancerous cell line HEK293. All the compounds had shown potential photocatalytic activity in degrading methylene-blue (MB).