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901228

Sigma-Aldrich

2-Ethylhexyl 4,6-dibromo-3-fluorothieno[3,4-b]thiophene-2-carboxylate

Synonym(s):

2-Ethylhexyl-4,6-dibromo-3-fluorothieno[3,2-c]thiophene-2-carboxylate

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About This Item

Empirical Formula (Hill Notation):
C15H17Br2FO2S2
CAS Number:
Molecular Weight:
472.23
MDL number:
UNSPSC Code:
12352101

assay

≥97%

form

powder

InChI

1S/C15H17Br2FO2S2/c1-3-5-6-8(4-2)7-20-15(19)12-10(18)9-11(21-12)14(17)22-13(9)16/h8H,3-7H2,1-2H3

InChI key

SOEJTOAKIMQIGL-UHFFFAOYSA-N

Application

2-Ethylhexyl 4,6-dibromo-3-fluorothieno[3,4-b]thiophene-2-carboxylate (TTF) can be used in the synthesis of diketopyrrolopyrrole (DPP) based low band polymers for the fabrication of organic field-effect transistors (OFETs). It can also be used in the synthesis of narrow band-gap polymers like PBDTT-OS-TT-EF (1.52 eV) and PBDTT-OS-TT-CF (1.56 eV) for polymeric solar cells.[1][2]

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Fine Tuning of Open-Circuit Voltage by Chlorination in Thieno[3,4-b]thiophene-Benzodithiophene Terpolymers toward Enhanced Solar Energy Conversion.
Qu S, et al.
Macromolecules, 50(13), 4962-4971 (2017)
PBDT-TSR: a highly efficient conjugated polymer for polymer solar cells with a regioregular structure.
Yao H, et al.
Journal of Material Chemistry A, 4(5), 1708-1713 (2016)
Toward high open-circuit voltage by smart chain engineering in 2D-conjugated polymer for polymer solar cells
Cheng X, et al.
Solar Energy Materials and Solar Cells, 149(82), 162-169 (2016)
An ultra-low bandgap diketopyrrolopyrrole (DPP)-based polymer with balanced ambipolar charge transport for organic field-effect transistors
Jiang T, et al.
Royal Society of Chemistry Advances, 6(82), 78720-78726 (2016)

Articles

Professor Chen (Nankai University, China) and his team explain the strategies behind their recent record-breaking organic solar cells, reaching a power conversion efficiency of 17.3%.

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