193265-36-0

Upstream product

• 1057140-05-2 5,15-dibromo-10,20-diphenylporphyrin 
• 21211-65-4 di(pyrrol-2-yl)methane 
• 100-52-7 benzaldehyde 
• 193265-35-9 C₃₂H₁₉BrN₄Ni 
• 160118-67-2 nickel(II) 5,15-diphenylporphyrin complex 
• 147470-60-8 [5,15-dibromo-10,20-diphenylporphyrinato]zinc 
• 22112-89-6 5,15-diphenylporphyrin 
• 1057140-05-2 5,15-dibromo-10,20-diphenylporphyrin 

Downstream Products

• 844466-45-1 (C₄H₂N)4(CC₆H₅)2C₂Ni(C₅H₄N)C₂(C₅H₄NCOCH₂) 
• 160118-67-2 nickel(II) 5,15-diphenylporphyrin complex 
• 1286199-71-0 C₆₄H₃₈N₈Ni₂ 
• 866916-89-4 5,15-[N,N'-bis(ethoxycarbonylamino)]diimino-10,20-diphenylporphodimethenatonickel(II) 
• 1351986-31-6 [5,15-diazido-10,20-diphenylporphyrinato]nickel(II) 
• 1279603-64-3 [5,15-bis(anthracen-9-yl)-10,20-diphenylporphyrinato]nickel(II) 
• 1122104-58-8 (2E,2'E)-dimethyl 3,3'-[(5,15-diphenylporphyrinato-10,20-diyl)-nickel(II)]diacrylate 
• 909039-63-0 [10,20-diphenylporphyrinatonickel(II)-5,15-diyl]bis(diphenylphosphine oxide) 
• 713136-04-0 [5-bromo-15-(4'-N,N-dimethylaminophenylethynyl)-10,20-diphenylporphyrinato]nickel(II) 
• 193265-41-7 nickel(II) 5,15-diphenyl-10,20-bis(2-trimethylsilylacetilenyl)porphyrinate 

Relevant academic research and scientific papers

Metal-catalyzed direct heteroarylation of C-H (: Meso) bonds in porphyrins: Facile synthesis and photophysical properties of novel meso -heteroaromatic appended porphyrins

A simple and rapid microwave-assisted synthesis of heteroaromatic appended porphyrins using the Pd/Cu-catalyzed C-C coupling of meso-bromoporphyrins with various five- and six-membered heteroaromatic azoles has been successfully developed. The prepared he

Efficient synthesis of meso-meso-linked diporphyrins by nickel(0)-mediated ullmann homocoupling

meso-meso-Linked diporphyrins have been prepared by nickel(0)-mediated Ullmann homocoupling under mild conditions. Georg Thieme Verlag Stuttgart - New York.

Porphyrin dimers and arrays

Current applications of porphyrins in medicine and optics, such as photodynamic therapy or nonlinear absorbers, increasingly require the use of far-red absorbing dyes. Modifications of the porphyrin structure to accommodate these conditions can be achieve

Functionalization of 5,15-diphenylporphyrin: Preparation and X-ray crystal structures of meso nitro, bromo, and trimethylsilylethynyl derivatives

Substitutions on 5,15-diphenylporphyrin led to the isolation of mono- and di-bromo and mono- and di-nitro derivatives, which were converted into their respective nickel(II) complexes. Reaction of the bromoporphyrins with iodine/silver nitrite resulted in nitrodebromination as well as conventional nitration. The nickel (II) complex of 5-nitro-10,20-diphenylporphyrin was reduced to the 5-amino derivative. The nickel(II) complexes of the bromoporphyrins were converted into the respective mono- and bis-(trimethylsilylethynyl) species. The crystal structures of 5-nitro-10,20-diphenylporphyrin, 5-bromo-10,20-diphenylporphyrinatonickel(II), and 10,20-diphenyl-5-(trimethylsilylethynyl)porphyrinatonickel(II) were determined.