Acceptors (38)

In polymer and polymer semiconductor building blocks, acceptor molecules are those capable of accepting electrons, leading to the formation of negatively charged ions or anions. These molecules are integral to the electronic characteristics of polymers and macromolecules, influencing their conductivity and semiconducting behavior. By incorporating acceptors into polymer semiconductors, the band gap can be adjusted, and charge transport properties improved. This makes them essential in applications such as organic solar cells, light-emitting diodes (LEDs), and transistors, where they contribute to enhancing device performance and efficiency.

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

Total: 19

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Acceptors (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