102202-48-2Relevant academic research and scientific papers
Synthesis of novel diselenide-linked porphyrin dimers under phase-transfer catalysis condition and their interactions with DNA
Xue, Zhi,Kwong, Daniel Wei-Jing,Xue, Ling-Wei,Liu, Qing,Hou, An-Xin,Wong, Wai-Kwok
, p. 1131 - 1143 (2009)
Novel diselenide-linked porphyrin dimers were synthesized under phase-transfer catalysis conditions. The targeted compounds were characterized by 1H-NMR, high-resolution mass spectrometry, UV/VIS and fluorescence spectroscopies, redox-potential
Mitochondria-targeting properties and photodynamic activities of porphyrin derivatives bearing cationic pendant
Lei, Wanhua,Xie, Jingfan,Hou, Yuanjun,Jiang, Guoyu,Zhang, Hongyan,Wang, Pengfei,Wang, Xuesong,Zhang, Baowen
experimental part, p. 167 - 171 (2011/10/30)
Four meso-tetraphenylporphyrin derivatives bearing either triphenylphosphonium ion-(P1 and P2) or triethylammonium ion-(P3 and P4) terminated alkoxy group at either para-(P1 and P3) or meta-(P2 and P4) position of one meso-phenyl group were designed and s
Structure effect on liotropic mesomorphism of the derivatives of tetrakis(4-sulfophenyl)porphyn. I. System linear dimer of tetrakis(4-sulfophenyl)porphyn sodium salt-ammonia-water
Bykova,Usol'tseva,Semeikin,Anan'eva,Kormilitsyn
, p. 614 - 618 (2007/10/03)
A synthesis was carried out, spectral characteristics and the double refraction were investigated of tetrakis(4-sulfophenyl)porphyn linear dimer in water-ammonia systems. The study of solvation processes revealed that the compound in question formed liomesophases.
SYNTHESIS OF TETRAPHENYLPORPHINES WITH ACTIVE GROUPS IN THE PHENYL RINGS. 4. FUNCTIONALLY SUBSTITUTED MONOHYDROXY DERIVATIVES OF TERAPHENYLPORPHINE
Syrbu, S. A.,Semeikin, A. S.,Koifman, O. I.,Berezin, B. D.
, p. 645 - 650 (2007/10/02)
Monosubstituted porphyrins bonded to 8-hydroxyquinoline, α-naphtalene, anthraquinone, and naphtoquinone residues, as well as dimeric porphyrins, were obtained by alkylation of monohydroxyphenyltriphenylporphines.
