4283-98-1

Upstream product

• 38274-14-5 2,2'-bis-(bromomethyl)-1,1'-biphenyl 
• 603-35-0 triphenylphosphine 

Downstream Products

• 30033-51-3 C₃₆H₂₈ 
• 30033-49-9 8-[1-(2'-Methyl-biphenyl-2-yl)-meth-(E)-ylidene]-bicyclo[4.2.0]octa-1,3,5-trien-7-one 
• 4284-00-8 2,2'-Bis-α-styryl-biphenyl 
• 35281-25-5 9,14-dihydrobenzo[f]tetraphene 
• 4284-01-9 2,2'-Diphenethyl-biphenyl 
• 28562-86-9 2,2'-Bis-<2-cyclohexyl-aethyl>-biphenyl 
• 30059-96-2 2-(2-o-Tolylphenethyl)-benzoesaeure 
• 30033-52-4 7-Methyl-8-[1-(2'-methyl-biphenyl-2-yl)-meth-(E)-ylidene]-bicyclo[4.2.0]octa-1,3,5-trien-7-ol 
• 30012-66-9 2-[(E)-2-(2'-Methyl-biphenyl-2-yl)-vinyl]-benzoic acid 
• 30012-65-8 2-Methyl-2'-(2-o-tolylethyl)biphenyl 
• 33612-04-3 1,2-Diphenyl-1,2,2a,10b-tetrahydro-cyclobuta[l]phenanthrene 
• 85-01-8 phenanthrene 
• 37445-18-4 C₄₂H₃₄ 
• 33510-35-9 bis(styryl)biphenyl 

Relevant academic research and scientific papers

Wittig reactions on photoprotoporphyrin IX: New synthetic models for the special pair of the photosynthetic reaction center

A first example of spirochlorin-chlorin dimer with fixed distances and orientations as potential model for the 'special pair' of the photosynthetic reaction center is discussed. For the preparation of such a novel structure, the Wittig reagent of the desired 'spacer' 5 was reacted with photoprotoporphyrin IX dimethyl ester 3 to produce the intermediate dimer 6, which on intramolecular [4 + 2] Diels-Alder cycloaddition gave an unexpected spirochlorin-chlorin dimer 9. Dehydration of dimer 6 under acid-catalyzed conditions generated the corresponding spirochlorinporphyrin dimer 16 in quantitative yield. The asymmetry in dimer 6 caused by the biphenyl-type anisotropic effect was confirmed by NMR and model studies. The formation of dihydrobenzoporphyrin 14 by reacting chlorin 3 with the phosphonium salt of p-methylbenzylbromide 10 and isolation of 8-phenanthrenevinylporphyrin 19 from chlorin 7 further confirmed our proposed mechanism for the formation of a spirochlorin-chlorin dimer 9. Following a similar approach, chlorin 3 on reacting with bis-phosphonium salt of 4,4'-bischloromethylbiphenyl produced conjugated chlorin dimer 25. The spectroscopic data obtained from these dimers suggest that, in these compounds, the individual chromophores are not behaving as an individual molecule, but as a single macrocycle. To examine whether the π-π interaction exhibited by dimer 9 resembles the structural arrangement of bacteriochlorophylls in reaction center (RC), we investigated the geometrical parameters used to characterize the π-π interactions in tetrapyrrolic macrocycles. Starting from the crystallographic coordinates of 9, the molecular mechanics energy minimization was performed to obtain the model dimer structure. The geometrical parameters that measure the single pyrrole ring overlap were used to compare the model structure with the crystallographic coordinates of the special pair in photosynthetic reaction center. The results indicated that the ring A of spirochlorin and the ring C of chlorin in our model dimer 9 mimic the ring A-ring A interaction found in the crystallographic special pairs, which are strategically placed by the surrounding photosynthetic reaction center protein matrix.

VO(acac)2-catalyzed oxidative coupling reactions of phosphonium salts

A novel eco-safer protocol for the preparation of symmetric or unsymmetric olefins directly from phosphonium salts under oxygen atmosphere in the presence of VO(acac)2 (1.0 mol%) was developed.