596104-74-4Relevant academic research and scientific papers
Aluminium(III) porphyrin based axial-bonding type dyads containing thiaporphyrins and expanded thiaporphyrins as axial ligands
Ghosh, Avijit,Maity, Dilip Kumar,Ravikanth, Mangalampalli
supporting information, p. 2630 - 2641 (2013/02/23)
Four axial-bonding type Al(III) porphyrin based dyads, containing thiaporphyrins with N3S 1 and N2S22 cores and expanded thaiporphyrins with N2S33 and N2S 44 cores, were synthesised by treating [(TPP)AlIIIOH] with the corresponding mono-functionalised meso-4-hydroxyphenyl thiaporphyrin or expanded thiaporphyrin building blocks in benzene at refluxing temperature. The stable dyads 1-4 are freely soluble in common organic solvents and characterized by mass, 1D and 2D NMR, absorption, electrochemical and fluorescence techniques. 1D and 2D NMR studies unambiguously confirmed the dyads. The absorption and electrochemical studies show weak interaction between the two macrocycles in dyads and the constituted macrocycles in dyads mostly retain their characteristic individual features. The steady state fluorescence studies indicate a decrease in the quantum yield of Al(III) porphyrin unit in dyads 1-4 and invoked the possibility of singlet-singlet energy transfer from the Al(III) porphyrin unit to the N3S porphyrin unit in dyad 1 and N 2S2 porphyrin unit in dyad 2. Structural information of these dyads in their ground (S0) state are generated by applying density functional theory (DFT) based quantum chemical calculations. Excited state calculations are carried out following time dependent density functional theory (TD-DFT) and UV-Vis spectra of these dyads are simulated in the Soret band region. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2012.
Novel and rapid synthetic routes to A3B- and AB3-type 21-thiaporphyrins and their use in the construction of unsymmetrical covalent and non-covalent porphyrin arrays
Gupta, Iti,Agarwal, Neeraj,Ravikanth, Mangalampalli
, p. 1693 - 1697 (2007/10/03)
Novel and very simple methods were developed for the synthesis of 21-thiaporphyrins having both one functional group (A3B) and three functional groups (AB3). These A3B- and AB 3-type 21-thiaporphyrin building bl
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
