| Identification | Back Directory | [Name]
2,5-Di(HD)-3,6-di(5-broMothiophen)diketopyrrolopyrrole | [CAS]
1000623-98-2 | [Synonyms]
DPP610-2Br
DPP-HD-2ThBr
2,5-Di(HD)-3,6-di(5-broMothiophen)diketopyrrolopyrrole
3,6-Bis(5-broMo-2-thienyl)-2,5-bis(2-hexyldecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione
3,6-bis(5-bromothiophen-2-yl)-2,5-bis(2-hexyldecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione
3,6-bis(5-bromo-2-thienyl)-2,5-dihydro-2,5-di(2'-hexyldecyl)-pyrrolo[3,4c]pyrrolo-1,4-dione
Pyrrolo[3,4-c]pyrrole-1,4-dione,3,6-bis(5-bromo-2-thienyl)-2-5-bis(2-hexyldecyl)-2,5-dihydro-
3,6-Bis(5-bromo-2-thienyl)-2,5-bis(2-hexyldecyl)-2,5-dihydro-pyrrolo[3,4-c]pyrrole-1,4-dione 98%
3,6-bis(5-broMo-2-thienyl)-2,5-bis(2-hexyldecyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione
DPP-iC16 | [Molecular Formula]
C46H70Br2N2O2S2 | [MDL Number]
MFCD28098664 | [MOL File]
1000623-98-2.mol | [Molecular Weight]
907 |
| Chemical Properties | Back Directory | [Melting point ]
110-115°C | [Boiling point ]
865.4±65.0 °C(Predicted) | [density ]
1.24±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [pka]
-5.29±0.60(Predicted) | [Odor]
Dark red/purple solid |
| Hazard Information | Back Directory | [Description]
3,6-bis(5-bromothiophen-2-yl)-2,5-bis(2-hexyldecyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione (DPP-HD-2ThBr) is a family member of?pyrrolopyrrole-dione (DPP). This monomer has been used for the synthesis of?PDPP3T, which is a low band-gap polymer semiconductor?commonly used?as i) a polymer donor material for OPV, and ii) hole-transport layer (HTL) for perovskite solar cells. | [Uses]
DDP-Br2 can be used in the fabrication of a variety of opto-electronic devices such as organic field effect transistors (OFETs), perovskite based solar cells, non-fullerene organic solar cells. | [General Description]
3,6-Bis(5-bromo-2-thienyl)-2,5-bis(2-hexyldecyl)-2,5-dihydro-pyrrolo[3,4-c]pyrrole-1,4-dione (DDP-Br2) belongs to the series of diketopyrrolopyrrole (DPP) based materials which show hole or ambipolar transport behavior with mobilities of charge carriers in the range of 0.1-1 cm2V-1 s-1. It has an electron deficient core that forms a low LUMO energy level which facilitates better air-stability for n-type organic semiconductors. |
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