Journal
RSC ADVANCES
Volume 10, Issue 12, Pages 6900-6918Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ra08504a
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- deanship of Scientific Research at Majmaah University, Saudi Arabia [R-1441-66]
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To examine the influence of both the important pi-acceptor character of the 4-cyanopyridine ligand and the nature of the para-substituted phenyls of meso-porphyrins on the electronic, electrochemical and structural properties of cobaltous metalloporphyrins, we prepared and fully characterized two coordination compounds: the (4-cyanopyridine)[meso-tetra(para-methoxyphenyl)porphyrinato]cobalt(ii) and the (4-cyanopyridine)[meso-tetra(para-chlorophenyl)porphyrinato]cobalt(ii) with the [Co-II(TMPP)(4-CNpy)] and [Co-II(TClPP)(4-CNpy)] formulas (complexes 1-2). The solution structures of compounds 1-2 were confirmed by H-1 NMR spectroscopy and mass spectrometry methods. They were further characterized by cyclic voltammetry and photoluminescence studies. The X-ray molecular structure data show that the Co-TClPP-4-NCpy derivative (2) exhibits high ruffling deformation compared to that of the Co-TMPP-4-CNpy species (1). Notably, the crystal packing of complex 1 shows the formation of CoMIDLINE HORIZONTAL ELLIPSISCo supramolecular dimers with a distance of 5.663 angstrom. As an application of our two cobaltous compounds, an investigation involving complexes 1-2 in the degradation of the methylene blue dye in the presence and absence of H2O2 in aqueous solutions was carried out. These promising results show that 1-2 can be used as catalysts in the degradation processes of dyes.
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