Photostability and fluorescence parameters of porphyrinoids: The effect of the macrocycle structure and the medium

[1]  A. Semeikin,et al.  Solvent-dependent tautomerism of the inverted isomer of meso-tetraphenylporphine: Effect of the polarity of the medium , 2016, Russian Journal of Physical Chemistry A.

[2]  A. Semeikin,et al.  Synthesis and physico-chemical properties of 2,7,12,17-tetraphenylporphycene and its metal complexes , 2015, Russian Journal of General Chemistry.

[3]  D. Berezin,et al.  Structure of porphyrin H-associates, inverted porphyrinoids, and corroles with N,N-dimethylformamide , 2014, Journal of Structural Chemistry.

[4]  J. Wojaczyński,et al.  Photooxidation of unhindered triarylcorroles , 2013 .

[5]  Lei Shi,et al.  Photophysical properties and singlet oxygen generation of three sets of halogenated corroles. , 2012, The journal of physical chemistry. B.

[6]  T. K. Chandrashekar,et al.  Meso-tetrakis(p-sulfonatophenyl)N-confused porphyrin tetrasodium salt: a potential sensitizer for photodynamic therapy. , 2012, Journal of medicinal chemistry.

[7]  M. Popiel,et al.  Common origin, common fate: regular porphyrin and N-confused porphyrin yield an identical tetrapyrrolic degradation product. , 2011, The Journal of organic chemistry.

[8]  D. R. Karimov,et al.  Thermal stability of porphyrins with chemicaly active NH bond and their associates with electron-donor solvents , 2011 .

[9]  M. Neves,et al.  How light affects 5,10,15-tris(pentafluorophenyl)corrole , 2010 .

[10]  P. A. Shatunov,et al.  Effect of ligand nonplanarity and solvent nature on the kinetic stability of zinc porphyrin complexes , 2008 .

[11]  Y. Ivanova,et al.  The acid properties of dodecasubstituted porphyrins with a chemically active NH bond , 2007 .

[12]  D. Berezin.  Criterion for estimate of NH bonds in porphyrin molecules , 2007 .

[13]  D. Modarelli,et al.  Photophysical Characterization of Free-Base N-Confused Tetraphenylporphyrins , 2002 .

[14]  Raymond Bonnett,et al.  Chemical Aspects of Photodynamic Therapy , 2000 .

[15]  J. Lindsey,et al.  An efficient one-flask synthesis of N-confused tetraphenylporphyrin. , 1999, Organic letters.

[16]  Á. Villanueva,et al.  SYNTHESIS OF 2,7,12,17-TETRAPHENYLPORPHYCENE (TPPO). FIRST ARYL-SUBSTITUTED PORPHYCENE FOR THE PHOTODYNAMIC THERAPY OF TUMORS , 1995 .

[17]  Kevin M. Smith,et al.  Photophysical properties of conformationally distorted metal-free porphyrins. Investigation into the deactivation mechanisms of the lowest excited singlet state , 1994 .

[18]  Tianhong Dai,et al.  Antimicrobial photodynamic inactivation and photodynamic therapy for infections. , 2010, Methods in molecular biology.

[19]  D. R. Karimov,et al.  Interaction of Porphyrins and Porphyrin Analogs with Coordinating Organic Solvents , 2009 .

[20]  I. Sazanovich,et al.  The photophysical and metal coordination properties of the N-CH3 substituted porphyrins: H(N-CH3)TPP vs H(CH3)OEP , 2005 .

[21]  R. Kumeev,et al.  The activation of NH bonds in tetrabenzoporphyrin molecules by electron-donor solvents , 2004 .

[22]  D. Berezin,et al.  Effect of a proton-donating solvent on the complexation of classical and nonclassical porphyrins in a pyridine medium , 2002 .

[23]  L. Latos‐Grażyński,et al.  N-methyltetraphenylporphyrin with an inverted N-methylpyrrole ring: the first isomer of N-methyltetraphenylporphyrin , 1995 .