Porphyrins

Recent work from the Doctorovich group at the University of Buenos Aires published in JACS identified the first biomimetic water-soluble FeII-porphyrin nitroxyl complexes. A pKa was calculated for the complex and reaction kinetics measured. DFT calculations implied the formation of a phlorin radical intermediate for the investigated reaction. Thanks for using our meso-tetra(4-sulfonatophenyl)porphine, T40699. 

Recent work from the Vesselli group at the University of Trieste published in Topics in Catalysis demonstrated both experimental and computational results for the metal-organic framework (MOF) structure of 5,10,15,20-tetra(4-pyridyl)21H,23H-porphyrin cobalt(III) chloride assembled on a Au(111) surface. The generated MOF was able to mimic O2 stabilization and activation mechanisms typically observed in proteins and enzymes. Thanks for using our cobalt tetrapyridylporphyrin, T40892. 

Cat. No: D40922 Cat. No: T40637 TyroSphere nanoparticles consisting of the triblock polymer [poly(ethyleneglycol)-block-oligio(desaminotyrosine octyl ester suberate)-block -poly(ethyleneglycol)] aggregates were loaded with amphiphilic porphyrins as reported by Tsubone, et al. Meso-cis-di(N-methyl-4-pyridyl)diphenylporphine dichloride Cat. No: D40922 , which is a positively charged porphyrin and meso-cis-di(4-sulfonatophenyl)-diphenylporphine dihydrochloride Cat. No: T40637, a negatively charged porphyrin were used. The