Product Details of 66-71-7. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 1,10-Phenanthroline, is researched, Molecular C12H8N2, CAS is 66-71-7, about Manganese(II) complexes of substituted salicylaldehydes and α-diimines: Synthesis, characterization and biological activity. Author is Ntanatsidis, Savvas; Perontsis, Spyros; Konstantopoulou, Sofia; Kalogiannis, Stavros; Hatzidimitriou, Antonios G.; Papadopoulos, Athanasios N.; Psomas, George.
The interaction of Mn+2 with substituted salicylaldehydes (X-saloH) gave five manganese(II) complexes formulated as [Μn(X-salo)2(MeOH)2]. When the reactions took place in the presence of an α-diimine such as 2,2′-bipyridine, 1,10-phenanthroline or 2,2′-bipyridylamine, five manganese(II) complexes [Mn(X-salo)2(α-diimine)] were isolated. The characterization of the complexes was accomplished by various spectroscopic techniques and single-crystal x-ray crystallog. The antioxidant activity of the compounds was evaluated via the scavenging of 1,1-diphenyl-picrylhydrazyl, 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) and hydroxyl free radicals. The antibacterial activity of the complexes was tested in vitro against Staphylococcus aureus and Xanthomonas campestris bacterial strains and was found moderate. Diverse techniques were employed to examine the interaction of the complexes with calf-thymus DNA which showed intercalation as the most possible interaction mode. The affinity of the complexes for bovine serum albumin was investigated by fluorescence emission spectroscopy and the binding constants were determined
There is still a lot of research devoted to this compound(SMILES：C1=CC3=C(C2=NC=CC=C12)N=CC=C3)Product Details of 66-71-7, and with the development of science, more effects of this compound(66-71-7) can be discovered.
Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics