299204-61-8

Upstream product

• 622-97-9 1-ethenyl-4-methylbenzene 
• 175614-52-5 (E)-1-(4-formyl)phenyl-2-(4-methyl)phenylethene 
• 117241-34-6 (E)-N-phenyl-3,4,5-tris(dodecyloxy)benzaldimine 
• 15164-44-0 p-(iodophenyl)carboxaldehyde 
• 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 

Downstream Products

• 299204-64-1 [4-((E)-2-{4-[(E)-2-(3,4,5-Tris-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-methanol 
• 370104-68-0 1,2,3-Tris-dodecyloxy-5-((E)-2-{4-[(E)-2-(4-vinyl-phenyl)-vinyl]-phenyl}-vinyl)-benzene 
• 950608-78-3 5,5-Dimethyl-2-(4-{(E)-2-[4-((E)-2-{4-[(E)-2-(3,4,5-tris-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-vinyl}-phenyl)-[1,3]dioxane 
• 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 
• 479499-97-3 N-(4-Nitro-phenyl)-N'-[1-[4-((E)-2-{4-[(E)-2-(3,4,5-tris-dodecyloxy-phenyl)-vinyl]-phenyl}-vinyl)-phenyl]-meth-(E)-ylidene]-hydrazine 

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

Synthesis and electronic properties of covalent assemblies of oligophenylenevinylene units arising from a calix[4]arene core

Assemblies of four oligophenylenevinylene moieties arising from a calix[4]arene core, i.e., calix[4]-oligophenylenevinylenes, have been prepared by Heck-type cross-coupling reactions of styrene derivatives with a tetraiodinated cone-calix[4]arene precursor. Photophysical studies in solution have revealed that there are electronic ground state interactions between the covalently bonded OPV moieties. The absorption spectra of the calix[4]oligophenylenevinylenes are significantly different from those obtained by summing the spectra of four model units and their emission is red-shifted when compared to the corresponding model compounds. Electrochemical studies have shown that the redox processes of the four OPV subunits do not take place at the same potentials indicating also a strong electronic interaction among them in the calix[4]oligophenylenevinylenes.

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