224966-39-6

Upstream product

• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 175614-52-5 (E)-1-(4-formyl)phenyl-2-(4-methyl)phenylethene 
• 106456-88-6 4-(5,5-dimethyl-1,3-dioxan-2-yl)benzaldehyde 
• 1530-37-6 (4-methylbenzyl)triphenylphosphonium chloride 
• 15164-44-0 p-(iodophenyl)carboxaldehyde 
• 622-97-9 1-ethenyl-4-methylbenzene 
• 299927-09-6 (Z)-1-[4-(4,4-dimethyl-2,6-dioxan-1-yl)phenyl]-2-(4-methylphenyl)ethene 
• 299927-05-2 5,5-dimethyl-2-[4-(2-p-tolyl-vinyl)-phenyl]-[1,3]dioxane 
• 1122-91-4 4-bromo-benzaldehyde 
• 105114-53-2 1-bromo-4-(5,5-dimethyl-1,3-dioxan-2-yl)benzene 

Downstream Products

• 299204-65-2 4-[4-((E)-2-{4-[(E)-2-(3,4,5-Tris-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-benzyloxy]-benzoic acid methyl ester 
• 299204-66-3 4-[4-((E)-2-{4-[(E)-2-(3,5-Bis-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-benzyloxy]-benzoic acid methyl ester 
• 272787-98-1 [4-((E)-2-{4-[(E)-2-(3,5-Bis-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-methanol 
• 299927-07-4 4-{(E)-2-[4-((E)-2-{4-[(E)-2-(3,5-Bis-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-vinyl}-benzaldehyde 
• 299927-06-3 1,3-Bis-dodecyloxy-5-((E)-2-{4-[(E)-2-(4-vinyl-phenyl)-vinyl]-phenyl}-vinyl)-benzene 
• 224966-54-5 4-((E)-2-{4-[(E)-2-(3,5-Bis-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-benzaldehyde 
• 299204-64-1 [4-((E)-2-{4-[(E)-2-(3,4,5-Tris-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-methanol 
• 299204-61-8 4-((E)-2-{4-[(E)-2-(3,4,5-Tris-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-benzaldehyde 
• 920966-73-0 C₆₃H₁₀₁O₆P 
• 299204-60-7 5,5-Dimethyl-2-[4-((E)-2-{4-[(E)-2-(3,4,5-tris-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-[1,3]dioxane 
• 224966-51-2 2-[4-((E)-2-{4-[(E)-2-(3,5-Bis-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-5,5-dimethyl-[1,3]dioxane 

Relevant academic research and scientific papers

Synthesis and excited-state properties of an oligophenylenevinylene heptamer substituted with two fullerene moieties

An oligophenylenevinylene (OPV) derivative substituted with two fullerene subunits has been prepared starting from a fullerene carboxylic acid derivative and an OPV heptamer bearing two alcohol functions. Photophysical investigations have revealed the occurrence of intramolecular photoinduced energy- and electron-transfer processes in this hybrid compound. Georg Thieme Verlag Stuttgart.

Fullerene - Oligophenylenevinylene hybrids: Synthesis, electronic properties, and incorporation in photovoltaic devices

Fullerene derivatives in which an oligophenylenevinylene (OPV) group is attached to C60 through a pyrrolidine ring have been prepared by 1,3-dipolar cycloaddition of the azomethine ylides generated in situ from the corresponding aldehydes and s

Synthesis of a C60-oligophenylenevinylene hybrid and its incorporation in a photovoltaic device

A fullefopyrrolidine derivative bearing an oligophenylenevinylene substituent has been prepared by 1,3-dipolar cycloaddition of an azomethine ylide to C60 and incorporated in a photovoltaic device.