The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 1,10-Phenanthroline, is researched, Molecular C12H8N2, CAS is 66-71-7, about Structural speciation in chemical reactivity profiling of binary-ternary systems of Ni(II) with iminodialcohol and aromatic chelators, the main research direction is preparation nickel iminodialc bipyridine phenanthroline complex reactivity luminescence dft.Reference of 1,10-Phenanthroline.
The importance of structural speciation in the control of chem. reactivity in Ni(II) binary-ternary systems, involving (O,O,N)-containing substrates (1,1′-iminodi-2-propanol), and aromatic chelators (2,2′-bipyridine, 1,10-phenanthroline), prompted the systematic synthesis of new crystalline materials characterized by elemental anal., FTIR, UV-Visible, Luminescence, magnetic susceptibility, and x-ray crystallog. The structures contain mononuclear octahedral assemblies, the lattice architecture of which exemplifies reaction conditions under which conformational variants and solvent-associated lattice-imposed complexes are assembled. Transformations between complex species denote their association with reactivity pathways, suggesting alternate synthetic methodologies for their isolation. Theor. work (Hirshfeld, Electrostatic Potential, DFT) signifies the impact of crystal structure on energy profiles of the generated species. The arisen physicochem. profiles of all compounds portray a well-configured interwoven network of pathways, projecting strong connection between structural speciation and Ni(II) reactivity patterns in organic-solvent media. The collective results provide well-defined parameterized profiles, poised to influence the synthesis of new Ni(II)-iminodialc. materials with specified structural-magneto-optical properties.
In some applications, this compound(66-71-7)Reference of 1,10-Phenanthroline is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.
Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics