1286685-45-7

Upstream product

• 1286685-39-9 trans-4,4,5,5-tetramethyl-2-(4-styryl-phenyl)[1,3]dioxolane 
• 1286685-12-8 triphenyl-[4-(4,4,5,5-tetramethyl[1,3]dioxolan-2-yl)benzyl]phosphonium bromide 
• 32555-96-7 4-styrylbenzaldehyde 
• 51359-78-5 4-(bromomethyl)benzaldehyde 
• 17201-43-3 4-cyanobenzyl bromide 
• 771577-73-2 2-(4-bromomethylphenyl)-4,4,5,5-tetramethyl-[1,3]dioxolane 

Relevant academic research and scientific papers

Harnessing "click"-type chemistry for the preparation of novel electronic materials

Sequence-independent or "click"-type chemistry is applied for the preparation of novel π-conjugated oligomers. A variety of bi-functional monomers for Wittig-Horner olefination are developed and applied in a sequential protection-deprotection process for the preparation of structurally similar π-conjugated oligomers. Selected oligomers are incorporated as the organic semiconductors in light-emitting diodes and a field-effect transistor, demonstrating the potential of the approach. Sequence-independent or "click"-type chemistry is applied for the preparation of novel π-conjugated oligomers. A variety of bi-functional monomers for Wittig-Horner olefination are developed and applied in a sequential protection-deprotection process for the preparation of structurally similar π-conjugated oligomers. Selected oligomers are incorporated as the organic semiconductors in light-emitting diodes and a field-effect transistor, demonstrating the potential of the approach.