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 Synthesis and characterization of non-aggregating octa-substituted azaphthalocyanines bearing bulky phenoxy substituents, published in 2008-09-08, which mentions a compound: 56413-95-7, mainly applied to azaphthalocyanine phenoxy preparation nucleophilic aromatic substitution phenol, Safety of 5,6-Dichloropyrazine-2,3-dicarbonitrile.
The synthesis and characterization of two novel series of octaazaphthalocyanines (AzaPc) bearing bulky phenoxy substituents are described. Target precursors to AzaPcs derivatives were prepared by using a nucleophilic aromatic substitution reaction between sterically hindered phenols (2,6-di-iso-propylphenol and 2,6-diphenylphenol) and 5,6-dichloropyrazine-2,3-dicarbonitrile. UV-vis and 1H NMR analyses confirm that steric isolation of the AzaPcs cores enforced both in the solution and in the solid state. This study explores the effectiveness of the steric factor imposed by the applied bulky phenoxy substituents on the packing behavior of azaphthalocyanines and thereby improving their solubility and photo-phys. properties.
As far as I know, this compound(56413-95-7)Safety of 5,6-Dichloropyrazine-2,3-dicarbonitrile can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.
Reference:
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate