1402411-12-4

Basic information

• Product Name: 4,4'-(5',5'''-(5-fluorobenzo[c][1,2,5]thiadiazole-4,7-diyl)bis([2'',2'''-bithiophene]-5'',5'-diyl))bis(N,N-diphenylaniline)
• CAS NO: 1402411-12-4
• Molecular Weight: 969.287
• Mol File: 1402411-12-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4,4'-(5',5'''-(5-fluorobenzo[c][1,2,5]thiadiazole-4,7-diyl)bis([2'',2'''-bithiophene]-5'',5'-diyl))bis(N,N-diphenylaniline)(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-(5',5'''-(5-fluorobenzo[c][1,2,5]thiadiazole-4,7-diyl)bis([2'',2'''-bithiophene]-5'',5'-diyl))bis(N,N-diphenylaniline)(1402411-12-4)
• EPA Substance Registry System: 4,4'-(5',5'''-(5-fluorobenzo[c][1,2,5]thiadiazole-4,7-diyl)bis([2'',2'''-bithiophene]-5'',5'-diyl))bis(N,N-diphenylaniline)(1402411-12-4)

Safety Data

• Hazardous Substances Data: 1402411-12-4(Hazardous Substances Data)

Upstream product

• 17821-75-9 5-fluorobenzo[c][1,2,5]thiadiazole 
• 367-31-7 4-fluoro-1,2-phenylenediamine 
• 36809-26-4 4-N,N-diphenylamino-1-bromobenzene 
• 1352921-50-6 4,7-bis(5-bromothiophen-2-yl)-5-fluorobenzo[c][1,2,5]thiadiazole 
• 1402411-14-6 5-{5-[4-(diphenylamino)phenyl]thiophen-2-yl}-2-(trimethylstannyl)pyrazine 
• 2369-11-1 5-fluoro-2-nitroaniline 
• 1352921-55-1 5-fluoro-4,7-di(thiophen-2-yl)benzo[c][1,2,5]thiadiazole 
• 1402411-11-3 5-fluoro-4,7-diiodobenzo[c][1,2,5]thiadiazole 

Relevant articles and documents

Facile synthesis of fluorine-substituted benzothiadiazole-based organic semiconductors and their use in solution-processed small-molecule organic solar cells

A facile new protocol for the synthesis of iodinated derivatives of fluorinated benzothiadiazoles is demonstrated for the production of p-type semiconducting materials. The newly synthesized small-molecule compounds bis[TPA-diTh]-MonoF-BT and bis[TPA-diTh]-DiF-BT exhibited a power conversion efficiency of 2.95 % and a high open-circuit voltage of 0.85 V in solution-processed small-molecule organic solar cells. A facile new protocol was developed for synthesis of iodinated derivatives of fluorinated benzothiadiazoles as precursors for fluorine-substituted benzothiadiazole-based organic semiconductors 2 and 3, which exhibit enhanced intramolecular charge transfer compared to unfluorinated analogue 1 and hence improved photovoltaic performance in small-molecule organic solar cells (see figure). Copyright