71248-63-0Relevant academic research and scientific papers
Convenient synthetic route of versatile 21-monothiatetraphenylporphyrins of the A4 and AB3 type
Stute, Silvio,Gloe, Kerstin,Gloe, Karsten
, p. 2907 - 2912 (2007/10/03)
A novel convenient synthetic route for poly-functional 21- monothiatetraphenylporphyrins of the type A4 und AB3 having base labile substituents in meso position was developed. Using this method a series of symmetric and asymmetric 21-thiaporphyrins containing different functional groups at the meso position is reported. The new products were characterized by NMR, UV-Vis and mass spectroscopy.
Water soluble, core-modified porphyrins. 3. Synthesis, photophysical properties, and in vitro studies of photosensitization, uptake, and localization with carboxylic acid-substituted derivatives
You, Youngjae,Gibson, Scott L.,Hilf, Russell,Davies, Sherry R.,Oseroff, Allan R.,Roy, Indrajit,Ohulchanskyy, Tymish Y.,Bergey, Earl J.,Detty, Michael R.
, p. 3734 - 3747 (2007/10/03)
Water soluble, core-modified porphyrins 1-5 bearing 1-4 carboxylic acid groups were prepared and evaluated in vitro as photosensitizers for photodynamic therapy. The 21,23-core-modified porphyrins 1-5 gave band I absorption maxima with λmax of
