Benzothiadiazoles and Analogs (965)

Benzothiadiazoles are heterocyclic compounds composed of a benzene ring fused with a thiadiazole ring. Known for their strong electron-accepting properties and excellent thermal stability, benzothiadiazoles and their derivatives can generate stable free radicals, making them valuable in semiconductor materials. In small-molecule semiconductors, they are commonly employed to enhance electron mobility and minimize recombination losses. Their adaptable chemistry enables the creation of diverse derivatives with customized properties.

2'-bromospiro[fluorene-9,9'-xanthene] structure diagram

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Benzothiadiazoles and Analogs (965)

2'-bromospiro[fluorene-9,9'-xanthene]

4-bromo-N,N-di-p-tolylaniline

3,7-dibromodibenzo[b,d]thiophene

dibenzo[b,d]furan-4-ylboronic acid

9-([1,1'-biphenyl]-4-yl)-3-(4-bromophenyl)-9H-carbazole

biphenylene

9H-fluorene-2,7-diamine

3,6-dibromophenanthrene-9,10-dione

N,N-diphenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline

thieno[2,3-c]furan-4,6-dione

1-(4-bromophenyl)-2-phenyl-1H-benzo[d]imidazole

anthracene-2-carboxylic acid

4-(4-bromophenyl)pyridine

anthracen-1-amine

1-iodonaphthalene

anthracen-9-ylboronic acid

1,1,2,2-tetraphenylethene

(9-ethyl-9H-carbazol-3-yl)boronic acid

9-bromo-7,7-dimethyl-7H-benzo[c]fluorene

naphthalen-1-ylboronic acid

4,4,5,5-tetramethyl-2-(4-(10-phenylanthracen-9-yl)phenyl)-1,3,2-dioxaborolane

2-iodonaphthalene

[1,1':4',1''-terphenyl]-2-ylboronic acid

1,4-dibromo-2,5-difluorobenzene

10-phenyl-10H-phenothiazine

3,5,6,8-tetrabromo-1,10-phenanthroline

N1,N1-bis(4-aminophenyl)benzene-1,4-diamine

(4-bromophenyl)diphenylphosphine oxide

5H-cyclopenta[2,1-b:3,4-b']dipyridin-5-one

5-chloro-1,10-phenanthroline