![4,7-Dibromobenzo[c]-1,2,5-thiadiazole (CAS 15155-41-6) - chemical structure image](https://media.scbt.com/product/4-7-dibromobenzoc-1-2-5-thiadiazole-15155-41-6-structure_17_67_b_176711.jpg)
![4,7-Dibromobenzo[c]-1,2,5-thiadiazole (CAS 15155-41-6) - chemical structure image](https://media.scbt.com/product/4-7-dibromobenzoc-1-2-5-thiadiazole-15155-41-6-structure_17_67_t_176711.jpg "Molecular structure of 4,7-Dibromobenzo[c]-1,2,5-thiadiazole, CAS Number: 15155-41-6")
4,7-Dibromobenzo[c]-1,2,5-thiadiazole (CAS 15155-41-6)
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4,7-Dibromobenzo[c]-1,2,5-thiadiazole functions as an electron-accepting material in organic electronic devices. It acts as a p-type semiconductor, facilitating the transport of positive charge carriers within the device. 4,7-Dibromobenzo[c]-1,2,5-thiadiazole exhibit high electron mobility and good stability, making it suitable for use in organic field-effect transistors and organic photovoltaic devices. The mechanism of action of 4,7-Dibromobenzo[c]-1,2,5-thiadiazole involves its ability to form strong intermolecular interactions with other organic semiconductors, leading to efficient charge transport and improved device performance. At the molecular level, 4,7-Dibromobenzo[c]-1,2,5-thiadiazole interacts with neighboring molecules to facilitate the movement of charge carriers.
4,7-Dibromobenzo[c]-1,2,5-thiadiazole (CAS 15155-41-6) References
- Cooperative Action for Molecular Debromination Reaction on Cu(110). | Sarasola, A., et al. 2018. J Am Chem Soc. 140: 15631-15634. PMID: 30394739
- In Situ Generation of Red-Emissive AIEgens from Commercial Sources for Nondoped OLEDs. | Yu, Y., et al. 2018. ACS Omega. 3: 16347-16356. PMID: 31458270
- Empowering non-covalent hydrogen, halogen, and [S-N]2 bonds in synergistic molecular assemblies on Au(111). | Barragán, A., et al. 2022. Nanoscale. 14: 17895-17899. PMID: 36458674
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4,7-Dibromobenzo[c]-1,2,5-thiadiazole, 1 g | sc-238994 | 1 g | $29.00 |