299204-64-1

Upstream product

• 622-97-9 1-ethenyl-4-methylbenzene 
• 15164-44-0 p-(iodophenyl)carboxaldehyde 
• 175614-52-5 (E)-1-(4-formyl)phenyl-2-(4-methyl)phenylethene 
• 117241-34-6 (E)-N-phenyl-3,4,5-tris(dodecyloxy)benzaldimine 
• 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 
• 224966-39-6 (E)-1-[4-(4,4-dimethyl-2,6-dioxan-1-yl)phenyl]-2-(4-methylphenyl)ethene 
• 299204-61-8 4-((E)-2-{4-[(E)-2-(3,4,5-Tris-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-benzaldehyde 

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 
• 920966-73-0 C₆₃H₁₀₁O₆P 

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.

Photoinduced processes in fullerenopyrrolidine and fullerenopyrazoline derivatives substituted with an oligophenylenevinylene moiety

Fullerene derivatives A-3PV and B-3PV in which an oligophenylenevinylene trimeric subunit (3PV) is attached to C60 through, respectively, a pyrrolidine or a pyrazoline ring have been prepared. The electrochemical and excited-state properties of

Columnar order in thermotropic mesophases of oligophenylenevinylene derivatives

Oligophenylenevinylene derivatives substituted with long alkyl chains on one end and a carboxylic acid function on the other end have been prepared and the dimeric polycatenar calamitic supramolecules resulting from hydrogen bonding of their acid function