IDTB6-2Sn has a structure of four hexylphenyl groups attached to an indaceno[1,2-b:5,6-b']dithiophene (IDT) core. IDTB6-2Sn has trimethylstannyl end functional groups for Stille coupling reaction to further extend its conjugation and enable absorption into the near-infrared region.
Part of our range of non-fullerene acceptor monomers, we stock high purity (>98%) IDTB6-2Sn for priority dispatch (lead times may apply for large quantities, please contact us for details). Qualifying orders ship free.
|Molecular weight||1233.03 g/mol|
|Classification / Family||Indaceno[1,2-b:5,6-b']dithiophene (IDT), Monomer and intermediates, None-fullerene acceptors (NFAs), NFA-OSCs, printing electronics|
|Purity||>98% (by NMR)|
|Appearance||Yellow crystalline powder|
Literature and Reviews
- Indacenodithiophene-Based Wide Bandgap Copolymers for High Performance Single-Junction and Tandem Polymer Solar Cells. Y.Ma et al., Nano Energy, 33, 313-324 (2017); DOI: 10.1016/j.nanoen.2017.01.050.
- A cyclopentadithiophene-bridged small molecule acceptor with near-infrared light absorption for efficient organic solar cells, Y. Yi et al, J. Mater. Chem. C, 7, 4013-4019 (2019); DOI: 10.1039/c9tc00162j.
- Efficient Semitransparent Solar Cells with High NIR Responsiveness Enabled by a Small-Bandgap Electron Acceptor, F. Liu et al., 29 (21), 1606574 (2017); DOI: 10.1002/adma.201606574.
- HOMO Energy Level Regulation of Novel Conjugated Copolymers for Polymer Solar Cells, J. Zhang et al., New J. Chem., 39, 6548-6554 (2015); DOI: 10.1039/C5NJ01105A.
- Solution-processed, indacenodithiophene-based, small-molecule organic field-effect transistors and solar cells, D. Liu et al., J. Mater. Chem. C, 2, 7523 (2014); DOI: 10.1039/c4tc00721b.
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