Analyzing the synthesis route of 66-71-7

After consulting a lot of data, we found that this compound(66-71-7)Name: 1,10-Phenanthroline can be used in many types of reactions. And in most cases, this compound has more advantages.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Slow relaxation of Dy(III) single-ion magnets dominated by the simultaneous binding of chelating ligands in low-symmetry ligand-fields, published in 2022, which mentions a compound: 66-71-7, mainly applied to dysprosium bipyridine phen salicylaldoxime complex preparation crystal structure magnetism, Name: 1,10-Phenanthroline.

Electronic effect and geometry distortion of low-symmetry ligand-field on the anisotropy barrier (Ueff) of spin reversal were compared in three Dy(III) single-ion magnets through the simultaneous binding of chelating ligands. The substitution of N,O-salicylaldoxime by N,N’-1,10-phenanthroline in the distorted triangular-dodecahedronal field sharply decreases the Ueff by 286 K due to an increase in nonpreferred transverse anisotropy, while the geometry distortion with CShM = 1.569 went down to 1.376 only lowering the Ueff by 12 K. The co-coordination strategy of heterodonor ligands highlights the importance of ligand-surroundings on the relaxation dynamics.

After consulting a lot of data, we found that this compound(66-71-7)Name: 1,10-Phenanthroline can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics