4,8-Bis-(5-hexyl-thiophen-2-yl)-2,6-bis-trimethylstannanyl-1,5-dithia-s-indacene
98%
- Product Code: 93978
CAS:
1403984-36-0
Molecular Weight: | 848.46 g./mol | Molecular Formula: | C₃₆H₅₀S₄Sn₂ |
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Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This chemical is primarily utilized in the field of organic electronics, particularly in the synthesis of conjugated polymers and small molecules for use in organic photovoltaic (OPV) devices. Its structure, featuring thiophene units and stannanyl groups, makes it a valuable building block for creating materials with desirable electronic properties. It is often employed in Stille coupling reactions, a key method for constructing π-conjugated systems, which are essential for efficient light absorption and charge transport in solar cells. Additionally, its incorporation into donor-acceptor copolymers can enhance the performance of organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs) by optimizing energy levels and improving charge carrier mobility. Its application contributes to the development of lightweight, flexible, and cost-effective electronic devices.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $322.08 |
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4,8-Bis-(5-hexyl-thiophen-2-yl)-2,6-bis-trimethylstannanyl-1,5-dithia-s-indacene
This chemical is primarily utilized in the field of organic electronics, particularly in the synthesis of conjugated polymers and small molecules for use in organic photovoltaic (OPV) devices. Its structure, featuring thiophene units and stannanyl groups, makes it a valuable building block for creating materials with desirable electronic properties. It is often employed in Stille coupling reactions, a key method for constructing π-conjugated systems, which are essential for efficient light absorption and charge transport in solar cells. Additionally, its incorporation into donor-acceptor copolymers can enhance the performance of organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs) by optimizing energy levels and improving charge carrier mobility. Its application contributes to the development of lightweight, flexible, and cost-effective electronic devices.
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