85111-02-0Relevant academic research and scientific papers
Supramolecular assemblies of phenolic metalloporphyrins: Structures and electrochemical studies
Quan, Gia Co,Denis, Morgane,Abeykoon, Brian,Tommasino, Jean-Bernard,Jeanneau, Erwann,Journet, Catherine,Devic, Thomas,Fateeva, Alexandra
, p. 103 - 116 (2019)
The reactivity of two phenolic porphyrins bearing respectively catechol and gallol-derived meso substituents (5,10,15,20-Tetrakis(3,4-dihydroxyphenyl)porphyrin and 5,10,15,20-Tetrakis(3,4,5-Trihydroxyphenyl)porphyrin) with trivalent metallic ions (Fe, Mn,
Preparation method of Meso-tetra(3,4-dimethoxy phenyl) porphyrin cobalt
-
Paragraph 0013; 0026; 0027, (2017/04/28)
The invention discloses a preparation method of Meso-tetra(3,4-dimethoxy phenyl) porphyrin cobalt, and belongs to the technical field of chemical synthesis and detection. The preparation method of the Meso-tetra(3,4-dimethoxy phenyl) porphyrin cobalt adop
Preparation method of Meso-tetra(3,4-dihydroxy phenyl) zinc porphyrin
-
Paragraph 0026; 0027, (2017/05/13)
The invention discloses a preparation method of Meso-tetra(3,4-dihydroxy phenyl) zinc porphyrin and belongs to the technical field of chemical synthesis and detection. The preparation method of Meso-tetra(3,4-dihydroxy phenyl) zinc porphyrin adopts raw ma
Supercapacitive hybrid materials from the thermolysis of porous coordination nanorods based on a catechol porphyrin
Jin, Shangbin,Hill, Jonathan P.,Ji, Qingmin,Shrestha, Lok Kumar,Ariga, Katsuhiko
supporting information, p. 5737 - 5744 (2016/05/24)
Synthesis of a series of porous coordination polymers with nanorod morphology constructed from a catechol-substituted porphyrin[meso-tetrakis(3,4-dihydroxyphenyl)porphyrin] is reported. While the coordination polymers had moderate surface areas (100-400 m
Porphyrin synthesis in surfactant solution: Multicomponent assembly in micelles
Bonar-Law, Richard P.
, p. 3623 - 3634 (2007/10/03)
A synthesis of meso-substituted porphyrins in anionic sodium dodecyl sulfate micelles has been developed. Polar, functionalized aromatic aldehydes condense reversibly with pyrrole in the micellar phase. Oxidation of the porphyrinogen then provides functionalized porphyrins in yields of 10-48%. Hydrophobic aldehydes condense irreversibly to give low yields at practical substrate concentrations. Synthesis in D2O solution results in per-β-deuterated porphyrins. A two-phase model is used to rationalize the dependence of porphyrin yield on reactant and surfactant concentration. Micelles are viewed as potential wells which promote porphyrinogen assembly by binding products more tightly than reactants.
PORPHYRINS AND THEIR DERIVATIVES. II. SYNTHESIS AND PROPERTIES OF MESO-TETRA(BENZO-18-CROWN-6)PORPHYRIN
Bogat-skii, A. V.,Zhilina, Z. I.,Stepanov, D. E.
, p. 2039 - 2042 (2007/10/02)
The previously undescribed meso-tetra(benzo-18-crown-6)porphyrin was obtained by the acid condensation of 4'-formylbenzo-18-crown-6 with pyrrole by the method of Treibs and Haberle and also by the reaction of meso-tetra(3,4-dihydroxyphenyl)porphyrin with
