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ChemicalBook--->CAS DataBase List--->109005-10-9

109005-10-9

109005-10-9 Structure

109005-10-9 Structure
IdentificationBack Directory
[Name]

10,15-Dihydro-5H-diindolo[3,2-a:3',2'-c]carbazole
[CAS]

109005-10-9
[Synonyms]

1',2'-c]fluorene
3',2'-c]carbazole
10,15-Dihydro-5H-diindolo[3,2-a
10,15-Dihydro-5H-5,10,15-triazaindeno[1,2-a
10,15-Dihydro-5H-diindolo[3,2-a:3',2'-c]...
10,15-Dihydro-5H-5,10,15-triaza-diindeno[1,2-
10,15-Dihydro-5H-diindolo[3,2-a:3',2'-c]carbazole
5H-Diindolo[3,2-a:3',2'-c]carbazole, 10,15-dihydro-
10,15-Dihydro-5H-5,10,15-triaza-diindeno[1,2-a:1,2-c]fluorene
[Molecular Formula]

C24H15N3
[MDL Number]

MFCD21609440
[MOL File]

109005-10-9.mol
[Molecular Weight]

345.396
Chemical PropertiesBack Directory
[Melting point ]

350°C(lit.)
[Boiling point ]

747.2±40.0 °C(Predicted)
[density ]

1.507±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

16.52±0.30(Predicted)
[color ]

White to Yellow to Green
[λmax]

342nm(DMSO)(lit.)
Safety DataBack Directory
[HS Code ]

2933.99.8290
Hazard InformationBack Directory
[Uses]

10,15-Dihydro-5H-diindolo[3,2-a:3',2'-c]carbazole, also known as triazacycloheptene (TAT), is a rotameric structure formed by fusing three indoles in orthogonal positions to a single benzene ring, or it can be viewed as a carbazole structure formed by fusing two indoles. In contrast to the carbazole unit, it is a C3 symmetric planar π-extended conjugated structure with a strong electron-carrying capacity, and usually acts as an electron-carrying component either alone or as part of a more complex structure. The triazatriene structure is an indole cyclic trimer with an extended non-localised π-system in which the three indole units form an overlapping framework. Due to the disc-like core, triazatricyclic heptene is highly susceptible to extended π planes, forming a columnar supramolecular arrangement. Organic semiconductors based on triazatricycloheptene have high hole mobility and are most often used as hole transport layer materials due to their strong π-π stacking ability.
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