1286685-34-4

Upstream product

• 198964-46-4 2,7-dibromo-9,9-dioctylfluorene 
• 534600-14-1 2-bromo-9,9-di-n-octylfluorene-7-carboxaldehyde 

Downstream Products

• 1286685-67-3 [4-(2-{4-[7-(2-{4-[7-(5,5-dimethyl-[1,3]dioxan-2-yl)-9,9-dioctyl-9H-fluorene-2-yl]-phenyl}-vinyl)-2,3-dihydro-thieno[3,4-b][1,4]dioxin-5-yl]-phenyl}-vinyl)-phenyl]-diphenylamine 
• 1286685-62-8 [4-(2-{4-[7-(5,5-dimethyl-[1,3]dioxan-2-yl)-9,9-dioctyl-9H-fluoren-2-yl]phenyl}-vinyl)-phenyl]-diphenylamine 

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.