173322-57-1Relevant articles and documents
Synthesis of meso-tetraphenylthiaporphyrins bearing one inverted pyrrole
Lee, Chang-Hee,Kim, Han-Je
, p. 3935 - 3938 (1997)
2-Aza-21-thia-23-carba-5,10,15,20-tetraphenylporphyrin and its N-methylated analogue were synthesized and characterized. The synthesis utilizers [3+1] condensation of thiatripyrrin with 2,4-bis(α-hydroxy-α-phenylmethyl)pyrrole or 2,4-bis(α-hydroxy-α-pheny
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
Synthesis of pseudoaromatic expanded porphyrin analogues
Lee,Oh
, p. 1921 - 1924 (2007/10/03)
Optically active expanded porphyrins bearing thiophene were synthesized by Schiff base forming reaction. The condensation of thiophene containing 1,14-bisformyl tripyrrane with aromatic diamines failed to give desired macrocycles but condensation with aliphatic 1,2-diamines gave the desired products. The macrocycles synthesized tend to maintain 18π system and the ethylene bridge shows somewhat resistance toward oxidation.
