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经验公式(希尔记法):
C8H4Br2S2
化学文摘社编号:
分子量:
324.06
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
InChI
1S/C8H4Br2S2/c9-5-1-3-11-7(5)8-6(10)2-4-12-8/h1-4H
SMILES string
Brc1ccsc1-c2sccc2Br
InChI key
KBRZCEVRNLKHAZ-UHFFFAOYSA-N
assay
97%
form
powder
mp
97-101 °C
Quality Level
Application
3,3′-Dibromo-2,2′-bithiophene can potentially be used in the designing and synthesis of a variety of optoelectronic and electronic devices, which include organic solar cells, thin film transistors, chemical sensors and photovoltaic cells.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Transistor Paint: Environmentally Stable N-alkyldithienopyrrole and Bithiazole-Based Copolymer Thin-Film Transistors Show Reproducible High Mobilities without Annealing
Liu J, et al.
Advances in Functional Materials, 19(21), 3427-3434 (2009)
Beyond efficiency: scalability of molecular donor materials for organic photovoltaics
Po R and Roncali J
Journal of Material Chemistry C, 4(17), 3677-3685 (2016)
Highly crystalline low-bandgap polymer nanowires towards high-performance thick-film organic solar cells exceeding 10% power conversion efficiency
Lee J, et al.
Energy & Environmental Science, 10(1), 247-257 (2017)
Quaterthiophene-Benzobisazole Copolymers for Photovoltaic Cells: Effect of Heteroatom Placement and Substitution on the Optical and Electronic Properties
Bhuwalka A, et al.
Macromolecules, 44(24), 9611-9617 (2011)
商品
Oligothiophenes are important organic electronic materials which can be produced using synthetic intermediates and Suzuki coupling.
Organic electronics promise renewable energy solutions surpassing silicon-based tech.
Professor Rivnay (Northwestern University, USA) discusses using organic mixed conductors as an alternative to efficiently bridge the ionic world of biology with contemporary microelectronics.
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