추천 제품
분석
≥97%
Quality Level
양식
powder
SMILES string
[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
애플리케이션
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).
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
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)
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
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)
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