3,6-Bis(5-broMothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione
3,6-Bis(5-broMothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione Basic information
- Product Name:
- 3,6-Bis(5-broMothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione
- Synonyms:
-
- 3,6-Bis(5-broMothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione
- DPP‐iC20
- 2,5-Di(OD)-3,6-di(5-broMothiophen)diketopyrrolopyrrole
- Pyrrolo[3,4-c]pyrrole-1,4-dione, 3,6-bis(5-bromo-2-thienyl)-2,5-dihydro-2,5-bis(2-octyldodecyl)-
- 1,4-bis(5-bromothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-3,6-dione
- DPP812-2Br
- 3,6-bis(5-broMothiophen-2-yl)-2,5-bis(2-oct
- 3,6-bis(5-bromothiophen-2-yl)-2,5-bis(2-octyldodecyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione
- CAS:
- 1260685-63-9
- MF:
- C54H86Br2N2O2S2
- MW:
- 1019.21
- Mol File:
- 1260685-63-9.mol
3,6-Bis(5-broMothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione Chemical Properties
- Melting point:
- 95.0-96.9℃ (hexane toluene )
- Boiling point:
- 925.3±65.0 °C(Predicted)
- Density
- 1.19±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- form
- solid
- pka
- -5.37±0.60(Predicted)
- color
- Dark purple
3,6-Bis(5-broMothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione Usage And Synthesis
Description
3,6-Bis(5-broMothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione contains a DPP moiety. The DPP moiety exhibits a planar conjugated bicyclic structure, which leads to strong π – π interactions that can allow for optimization of the performance of organic semiconductors. Moreover, the introduction of branched long alkyl chains to the N-position of the lactam ring affords control over physical properties such as solubility, crystallization, and selfassembly capacity.
Uses
3,6-Bis(5-bromothien-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4-dione is an intermediate in the synthesis of DPPT-TT which are organic thin-film transistors.
References
1.Effect of Selenophene in a DPP Copolymer Incorporating a Vinyl Group for High-Performance Organic Field-Effect Transistors, I. Kang et al., Adv. Mater., 25, 524-528 (2013).
3,6-Bis(5-broMothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dioneSupplier
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3,6-Bis(5-broMothiophen-2-yl)-2,5-bis(2-octyldodecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione(1260685-63-9)Related Product Information
- Pyrrolo[3,4-c]pyrrole-1,4-dione, 3,6-bis(5-bromo-2-thienyl)-2,5-dihydro-
- 3,6-Di(2-thienyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione
- 3,4-Dimethoxythiophene
- 2,5-Di(HD)-3,6-di(5-broMothiophen)diketopyrrolopyrrole
- 3,6-DIBROMOTHIENO[3,2-B]THIOPHENE
- 3,6-Di(thieno[3,2-b]thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione
- 3,6-bis(5-broMo-4-(2-ethylhexyl)thiophen-2-yl)-1,2,4,5-tetrazine
- 3,6-Bis(5-bromo-2-thienyl)-2,5-dihydro-2,5-dioctylpyrrolo[3,4-c]pyrrole-1,4-dione
- 4,4'-Dibutoxy-2,2'-bis(trimethylstannyl)-5,5'-bithiazole
- DPP‐iC12
- 3,4-Dibromothiophene
- 3,6-Bis(5-bromo-2-thienyl)-2,5-bis(2-ethylhexyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione