(4,8-Bis(5-(2-butyloctyl)-4-fluorothiophen-2-yl)benzo[1,2-b:4,5-b']dithiophene-2,6-diyl)bis(trimethylstannane)
98%
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Used primarily in organic electronics, this compound serves as a key intermediate in the synthesis of conjugated polymers for high-performance organic semiconductors. It is especially valuable in the preparation of donor-acceptor copolymers used in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The presence of fluorinated thiophene units enhances electron affinity and improves charge carrier mobility, while the trimethylstannane groups enable efficient Stille coupling reactions during polymerization. Its branched alkyl side chains contribute to good solubility in organic solvents, facilitating solution-processing techniques like spin-coating and inkjet printing. This makes the material suitable for flexible, large-area electronic devices.
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