推荐产品
![4,7-二溴苯并[c]-1,2,5-噻二唑 95%](/deepweb/assets/sigmaaldrich/product/structures/711/964/3fd3ffd1-5916-468e-a743-22f1611b5a33/640/3fd3ffd1-5916-468e-a743-22f1611b5a33.png)
![2-[(7-Bromo-2,1,3-benzothiadiazol-4-yl)methylene]malononitrile ≥97%](/deepweb/assets/sigmaaldrich/product/structures/284/951/2311af80-f182-4a47-962b-690f690f49aa/640/2311af80-f182-4a47-962b-690f690f49aa.png)
方案
>97%
表单
powder
mp
144-149 °C
SMILES字符串
BrC1=CN=C(Br)C2=NSN=C21
InChI
1S/C5HBr2N3S/c6-2-1-8-5(7)4-3(2)9-11-10-4/h1H
InChI key
LEHZIBSAFRVAJP-UHFFFAOYSA-N
一般描述
4,7-Dibromo-[1,2,5]thiadiazolo[3,4-c]pyridine is a thiadiazolo[3,4-c]pyridine based material that is used as an electron deficient group for organic electronic applications.
应用
4,7-Dibromo-[1,2,5]thiadiazolo[3,4-c]pyridine can be used in the synthesis of panchromatic organic for dye sensitized solar cells (DSSCs).
This product is used in the synthesis of photoactive acceptor part in low band gap conjugated polymers and oligomers for high performance OPV devices.
警示用语：
Danger
危险分类
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Chalcogenodiazolo [3, 4-c] pyridine based donor-acceptor-donor polymers for green and near-infrared electrochromics
Ming S, et al.
Polym. Chem., 6(48), 8248-8258 (2015)
Solution-processed small-molecule solar cells with 6.7% efficiency
Sun, Yanming; Welch, Gregory C.; Leong, Wei Lin; et al.
Nature Materials, 11(1), 44-48 (2012)
Regioregular pyridyl [2, 1, 3] thiadiazole-co-indacenodithiophene conjugated polymers
Wen W, et al.
Chemical Communications (Cambridge, England), 49(65), 7192-7194 (2013)
Nicolas Blouin et al.
Journal of the American Chemical Society, 130(2), 732-742 (2007-12-22)
On the basis of theoretical models and calculations, several alternating polymeric structures have been investigated to develop optimized poly(2,7-carbazole) derivatives for solar cell applications. Selected low band gap alternating copolymers have been obtained via a Suzuki coupling reaction. A good
Effects of various pi-conjugated spacers in thiadiazole [3, 4-c] pyridine-cored panchromatic organic dyes for dye-sensitized solar cells
Hua Y, et al.
Journal of Material Chemistry A, 3(6), 3103-3112 (2015)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门