Synthetic Route of C12H8N2. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 1,10-Phenanthroline, is researched, Molecular C12H8N2, CAS is 66-71-7, about Synthesis, characterization, crystallographic structure, theoretical studies, and in vitro cytotoxicity assessment of two Gd(III) and Ce(IV) complexes containing pyridine-2,6-dicarboxylate. Author is Zohrevandi, Mina; Abdolmaleki, Sara; Ghadermazi, Mohammad; Gholiee, Yasin; Aliabadi, Alireza; Motieiyan, Elham; Hakimi, Mohammad; Marabello, Domenica.
This paper reports the synthesis of two complexes through one-pot reactions of pyridine-2,6-dicarboxylic acid (pydcH2), phenanthroline, and 2-aminopyridine, with Gd(NO3)3·6H2O and Ce (NO3)3·6H2O metal salts. The new coordination complexes C1 and C2 were identified by spectroscopic methods. The complexes were characterized by x-ray crystallog. The nature of metal-ligand interactions was studied theor. using NBO and EDA-NOCV analyses. The results showed that the contribution of electrostatic interactions in both complexes is considerably larger than that of orbital. However, the contribution of orbital interactions in [CeL3]2-, is more than that in [GdL3]3- (28.8% vs. 21.8%). In following, the cytotoxic effect of synthetic complexes was investigated in vitro using oxaliplatin as a standard against three cancer cell lines including human breast cancer (MCF7), human colon adenocarcinoma (HT29), human lymphocyte (HL60) and also one normal cell, human foreskin fibroblast (HFF). The most significant inhibition activity was observed by both C1 (IC50 = 80.7 μM, Viability inhibition = 83.41%) and C2 (IC50 = 98.3 μM, Viability inhibition = 77.19%) toward the MCF7 cell line.
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