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The first five-membered-heterocycle-fused subphthalocyanine analogues: chiral tri(benzo[b]thiopheno)subporphyrazines.
Nature of the intense second-order nonlinear optical activity: DFT studies on the octupolarization of sandwich-type bis(phthalocyaninato) yttrium skeletons.
Four dibutylamino substituents are better than eight in modulating the electronic structure and third-Order nonlinear-Optical properties of phthalocyanines.
Porphyrin–Alkaline earth MOFs with the highest adsorption capacity for methylene blue.
Sandwich rare earth complexes simultaneously involving aromatic phthalocyanine and antiaromatic hemiporphyrazine ligands showing a predominantly aromatic nature.

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