757225
Thieno[3,2-b]thiophene-2,5-dicarboxaldehyde
96%
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About This Item
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Assay
96%
form
solid
mp
274-277 °C
storage temp.
2-8°C
SMILES string
O=Cc1cc2sc(C=O)cc2s1
InChI
1S/C8H4O2S2/c9-3-5-1-7-8(11-5)2-6(4-10)12-7/h1-4H
InChI key
UBKNFAFBINVTOP-UHFFFAOYSA-N
Application
This molecule has been used in the synthesis of novel metal-free organic dyes for Dye-Sensitized Solar Cells reaching conversion efficiencies of 6.23%.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Chemical communications (Cambridge, England), 26(26), 2792-2794 (2006-10-03)
Two novel metal-free organic dyes containing thienothiophene and thiophene segments have been synthesized. Nano-crystalline TiO2 dye-sensitized solar cells were fabricated using these dyes as light-harvesting sensitizers, and a high solar energy-to-electricity conversion efficiency of 6.23% was achieved.
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Covalent organic frameworks (COFs), consisting of covalently connected organic building units, combine attractive features such as crystallinity, open porosity and widely tunable physical properties. For optoelectronic applications, the incorporation of heteroatoms into a 2D COF has the potential to yield
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