Donor-Acceptor (DA) Type Monomers (38)

Donor-acceptor (DA) type monomers serve as molecular building blocks that integrate electron donor and acceptor units within a single structure. These monomers play a vital role in the development of polymer semiconductors, as they enable precise tuning of electronic properties for targeted applications. The DA configuration promotes intramolecular charge transfer, leading to distinctive optical and electrical characteristics. Consequently, DA-type monomers are widely utilized in organic electronics, including organic photovoltaics, field-effect transistors, and sensors, where their unique properties improve device performance and functionality.

2,5-dibromothiophene 1,1-dioxide structure diagram

Total: 19

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Donor-Acceptor (DA) Type Monomers (38)

2,5-dibromothiophene 1,1-dioxide

4,7-dibromobenzo[c][1,2,5]selenadiazole

4,7-dibromo-5-fluorobenzo[c][1,2,5]thiadiazole

4,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazole

1,3-dibromo-5-(2-ethylhexyl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione

10,10'-dibromo-9,9'-bianthracene

naphtho[1,2-c:5,6-c']bis([1,2,5]thiadiazole)

4,7-bis(5-bromothiophen-2-yl)benzo[c][1,2,5]thiadiazole

2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9'-spirobi[fluorene]

2,5-Dibromo-3-hexadecylthiophene

2,2'-(9,9-dimethyl-9H-fluorene-2,7-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)

5,12-dibromoanthra[2,1,9-def:6,5,10-d'e'f']diisochromene-1,3,8,10-tetraone

(9,9-dimethyl-9H-fluorene-2,7-diyl)diboronic acid

4,7-dibromo-5,6-difluorobenzo[c][1,2,5]thiadiazole

4,9-dibromoisochromeno[6,5,4-def]isochromene-1,3,6,8-tetraone

(Z)-6,6'-dibromo-1,1'-bis(2-ethylhexyl)-[3,3'-biindolinylidene]-2,2'-dione

5-octyl-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione

spiro[fluorene-9,9'-xanthene]-3',6'-diol

4,7-di(thiophen-2-yl)benzo[c][1,2,5]thiadiazole