1339098-85-9

Upstream product

• 1187422-99-6 2-bromo-4,9-dihydro-4,4,9,9-(p-hexoxyphenyl)-s-indaceno[1,2-b:5,6-b']dithiophene 
• 101-70-2 bis(4-methoxyphenyl)amine 
• 1187422-97-4 4,9-dihydro-4,4,9,9-(p-hexoxyphenyl)-s-indaceno[1,2-b:5,6-b']dithiophene 
• 1187422-93-0 2,5-bis-(5-trimethylsilanyl-thiophen-2-yl)-terephthalic acid diethyl ester 
• 915224-39-4 diethyl 1,4-bis(thiophen-2-yl)-2,5-benzenedicarboxylate 

Downstream Products

• 1339098-93-9 2-[N,N-bis(p-methoxyphenyl)amino]-4,9-dihydro-4,4,9,9-(p-hexoxyphen-yl)-7-formyl-s-indaceno[1,2-b:5,6-b']dithiophene 

Relevant academic research and scientific papers

Organic dyes containing a coplanar indacenodithiophene bridge for high-performance dye-sensitized solar cells

A series of new organic dyes exploiting coplanar indacenodithiophene as the central π-spacer of the classical donor-(π-spacer)-acceptor configuration were synthesized and characterized for dye-sensitized solar cells. The coplanarity of the indacenodithiophene core facilitates efficient donor to acceptor charge transfer, imparting the new organic dyes significant bathochromic shifts and remarkable power conversion efficiencies of up to 6.7% (DTInDT) under AM 1.5G radiation.