|Molecular weight||904.57 g/mol|
|Classification / Family||Thiophene, Fused thiophene, Benzo-dithiophene heterocylic aromatics, Five-membered ring, Semiconductor synthesis intermediates, Low band gap polymers, OFETs, Organic photovoltaics, Polymer solar cells|
|Purity||>99% (by HPLC)|
|Appearance||Light yellow crystals|
2,6-Bis(trimethytin)-4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b’]dithiophene has been used for the synthesis of small molecules and low band gap polymer semiconductors such as PTB-7, PCE10 (also called PTB7-Th or PBDTTT-EFT) and PBDB-T (PCE12) for OFETs, OLED, PLED, OPV applications.
Bearing two ethylhexyl alkyl side chains, with fused thiophenes and thiophenes as electron-rich pendants, 2,6-bis(trimethytin)-4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b’]dithiophene offers good solubility for synthesis of polymer chains.
Literature and Reviews
- Enhanced performance for organic bulk heterojunction solar cells by cooperative assembly of ter(ethylene oxide) pendants, L. Chen et al., Polym. Chem., 5, 4480-4487 (2014); DOI: 10.1039/C4PY00095A.
- Breaking the 10% Efficiency Barrier in Organic Photovoltaics: Morphology and Device Optimization of Well-Known PBDTTT Polymers, Adv. Energy Mater., 6, 1502529 (2016), S. Zhang et al., DOI: 10.1002/aenm.201502529.
- Study of Optical Properties and Molecular Aggregation of Conjugated Low Band Gap Copolymers: PTB7 and PTB7-Th, F. Bencheikh et al., J. Phys. Chem. C 2015, 119, 24643−24648 (2015); DOI: 10.1021/acs.jpcc.5b07803.
To the best of our knowledge the technical information provided here is accurate. However, Ossila assume no liability for the accuracy of this information. The values provided here are typical at the time of manufacture and may vary over time and from batch to batch.