“…However, such systems are even less studied (for the same reason). A number of phthalocyanine analogues are known that contain polycyclic aromatic hydrocarbon rings instead of benzene rings (for example, 2,3-naphthalocyanines, Nc 3), as well as heterocyclic fragments [13][14][15]; tetraazaporphyrins 4 (porphyrazines, Pz) [16], the tetrabenzo derivatives of which are phthalocyanines themselves; subphthalocyanines (SubPc, 5) [17] and superphthalocyanines (SPc, 6). When preparing metal complexes of phthalocyanines from acids, anhydrides or imides, a source of nitrogen atoms is needed to form phthalocyanine, usually urea.…”