Donor Monomers (38)

Donor monomers are molecules that contribute electrons, resulting in the formation of positively charged ions or cations within polymer or polymer semiconductor structures. These monomers play a critical role in adjusting the electronic properties of polymers, influencing their conductivity, luminescence, and charge transport behavior. Typically paired with acceptor monomers, donor monomers are used to create donor-acceptor copolymers with tailored electronic characteristics. Their applications span organic light-emitting diodes (OLEDs), solar cells, and transistors, where they enhance the efficiency, stability, and overall performance of these devices.

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

Total: 19

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Donor 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