1385014-52-7

Upstream product

• 100943-46-2 5-hexylthiophene-2-carbaldehyde 
• 1385014-51-6 (E,E)-3,5-bis[2-(5-hexylthiophen-2-yl)vinyl]benzoic acid 
• 1202493-19-3 methyl 3,5-bis[(diethoxyphosphoryl)methyl]benzoate 

Downstream Products

• 1385014-53-8 (E,E)-3,5-bis[2-(5-hexylthiophen-2-yl)vinyl]benzyl iodide 
• 1385014-54-9 diethyl (E,E)-3,5-bis[2-(5-hexylthiophen-2-yl)vinyl]benzylphosphonate 
• 1385014-60-7 (E,E,E,E,E,E)-2,5-bis{3,5-bis[2-(5-hexylthiophen-2-yl)vinyl]styryl}thiophene 

Relevant academic research and scientific papers

Layer-block dendrimers with alternating thienylenevinylene and phenylenevinylene units

A series of new hybrid, layer-block π-conjugated dendrons and dendrimers with alternating thienylenevinylene and phenylenevinylene units has been prepared by means of an orthogonal and convergent-growth methodology that made use of the Horner-Wadsworth-Emmons (HWE) reaction. The placement of the thiophene and benzene rings can be accurately controlled to afford a large variety of dendritic structures, although access to compounds of high generation proved difficult. The optical properties of the synthesized dendrimers were determined by UV/vis and fluorescence spectroscopy, and the influence of the generation and nature of the core on the behavior of these materials was evaluated.