推荐产品
方案
≥97%
质量水平
表单
powder
SMILES字符串
[s]1c(ccc1c2[s]c(c4c2C(=O)c5c(c([s]c5CC(CCCC)CC)CC(CCCC)CC)C4=O)c3[s]c(cc3)Br)Br
InChI
1S/C34H38Br2O2S4/c1-5-9-11-19(7-3)17-23-27-28(24(39-23)18-20(8-4)12-10-6-2)32(38)30-29(31(27)37)33(21-13-15-25(35)40-21)42-34(30)22-14-16-26(36)41-22/h13-16,19-20H,5-12,17-18H2,1-4H3
InChI key
HETICFAGRUKZDA-UHFFFAOYSA-N
应用
1,3-Bis(5-bromo-2-thienyl)-5,7-bis(2-ethylhexyl)-4H,8H-benzo[1,2-c:4,5-c′]dithiophene-4,8-dione (BDD), a strong electron accepting molecule, can be used in the fabrication of non-fullerene polymeric solar cells. It can also be used in the synthesis of a new conjugated polymer, 5,7-bis(2- ethylhexyl)benzo[1,2-c:4,5-c′]dithiophene-4,8-dione (PBDTBDD).
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
High-efficiency non-fullerene polymer solar cell fabricated by a simple process using new conjugated terpolymers
Hoang MH, et al.
Journal of Material Chemistry C, 7(1), 111-118 (2019)
Wenchao Zhao et al.
Journal of the American Chemical Society, 139(21), 7148-7151 (2017-05-18)
A new polymer donor (PBDB-T-SF) and a new small molecule acceptor (IT-4F) for fullerene-free organic solar cells (OSCs) were designed and synthesized. The influences of fluorination on the absorption spectra, molecular energy levels, and charge mobilities of the donor and
Molecular Optimization Enables over 13% Efficiency in Organic Solar Cells.
Zhao W, et al.
Journal of the American Chemical Society, 139(21), 7148-7151 (2017)
Single-junction organic solar cells based on a novel wide-bandgap polymer with efficiency of 9.7%.
Lijun Huo et al.
Advanced materials (Deerfield Beach, Fla.), 27(18), 2938-2944 (2015-04-03)
Design, Application, and Morphology Study of a New Photovoltaic Polymer with Strong Aggregation in Solution State.
Qian D, et al.
Macromolecules, 45(24), 9611-9617 (2012)
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