Identification | Back Directory | [Name]
3,4-Dithia-7H-cyclopenta[a]pentalene | [CAS]
389-58-2 | [Synonyms]
DTCPP S1371 (389-58-2) 3,4-b']dithiophene 4H-Cyclopenta[2,1-b H-Cyclopenta[2,1-b:3,4-b 4H-Cyclopenta[2,1-b:3,4-b 3,4-Dithia-7H-cyclopenta[a]pentalene 4H-Cyclopenta[2,1-b:3,4-b']dithiophene 4H-cyclopenta[1,2-b:5,4-b']dithiophene 4H-cyclopenta[1,2-b:5,4-b']bisthiophene 4H-Cyclopenta[2,1-b:3,4-b']dithiophene > 2,6-Dibromo-4,4-dibutyl-4H-cyclopenta[2,1-b 2,6-Dibromo-4,4-bis-(6-bromo-hexyl)-4H-cyclopenta[2,1-b 4H-Cyclopenta[2,1-b:3,4-b']dithiophene 2,6-DIBROMO-4,4-DIBUTYL-4H-CYCLOPENTA[2,1-B;3,4-B']DITHIOPHENE | [EINECS(EC#)]
1592732-453-0 | [Molecular Formula]
C9H6S2 | [MDL Number]
MFCD20133900 | [MOL File]
389-58-2.mol | [Molecular Weight]
178.27 |
Chemical Properties | Back Directory | [Melting point ]
71.0 to 75.0 °C | [Boiling point ]
307.8±22.0 °C(Predicted) | [density ]
1.400 | [storage temp. ]
0-10°C | [solubility ]
soluble in Toluene | [form ]
powder to crystal | [color ]
White to Light yellow to Dark green | [λmax]
305nm(EtOH)(lit.) | [InChIKey]
UITASDKJJNYORO-UHFFFAOYSA-N | [CAS DataBase Reference]
389-58-2 | [Description]
4H-cyclopenta[2,1-b:3,4-b′]dithiophene, also known as CPDT, a rigid coplanar structure favouring π?π intermolecular interactions with good electron-donating properties, has been one of the most attractive building blocks for organic field effect transistors and organic electronics. The five-member ring in the middle also offer the function to have side-chain manipulation to enhance solubility in solutions for device fabrications, morphology and polymer processing. One of the intensively studied polymer for organic electrons, PCPDTBT, with the alternating CPDT and 2,1,3- benzothiadiazole (BT) units, has demonstrated device performance of PCE over 6% [5] | [Odor]
Off-white powder |
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