11,12-Dihydro-11-phenylindolo[2,3-a]carbazole
11,12-Dihydro-11-phenylindolo[2,3-A]carbazole
CAS: 1024598-06-8
Molecular Formula: C24H16N2
11,12-Dihydro-11-phenylindolo[2,3-a]carbazole - Names and Identifiers
11,12-Dihydro-11-phenylindolo[2,3-a]carbazole - Physico-chemical Properties
| Molecular Formula | C24H16N2 |
| Molar Mass | 332.4 |
| Density | 1.26 |
| Boling Point | 598.8±32.0 °C(Predicted) |
| Appearance | powder to crystal |
| Color | White to Light yellow to Light orange |
| pKa | 16.78±0.30(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
11,12-Dihydro-11-phenylindolo[2,3-a]carbazole - Introduction
11-Phenyl -11, 12-indoline [2,3-a] arocarbazole is an organic compound, often abbreviated as DBT. The following is a description of its nature, use, preparation and safety information:
Nature:
1. Appearance: DBT is a colorless crystalline solid.
2. melting point: about 180-187 degrees Celsius.
3. Solubility: DBT is soluble in common organic solvents.
Use:
1. Transition metal complexes: DBT can be used as a ligand to form stable complexes with transition metals, which are used in catalysts, photosensitizers and other related fields.
2. Photoelectric materials: DBT has good photoelectric properties and can be used in the preparation of organic optoelectronic devices, such as organic photodiodes (OLED) and photovoltaic cells.
3. curve structure: because of its special molecular structure, DBT can be used to build surface network structure and electronic structures.
Preparation Method:
DBT can be prepared in a variety of ways, common methods include:
1. Chemical synthesis: DBT is obtained by organic synthesis reaction, for example, reaction with anisole and acrolein, and then cyclization reaction.
2. Metal catalysis: DBT is obtained by coupling reaction of diphenyl imine and pyrrole acetal in the presence of a metal catalyst.
Safety Information:
1. DBT has no obvious harm to human health under ordinary operating conditions.
2. When handling DBT, follow routine laboratory practices, such as wearing personal protective equipment such as protective gloves, glasses, and laboratory coats.
3. DBT should be stored in a cool and dry place, and away from fire and oxidizing agents.
Nature:
1. Appearance: DBT is a colorless crystalline solid.
2. melting point: about 180-187 degrees Celsius.
3. Solubility: DBT is soluble in common organic solvents.
Use:
1. Transition metal complexes: DBT can be used as a ligand to form stable complexes with transition metals, which are used in catalysts, photosensitizers and other related fields.
2. Photoelectric materials: DBT has good photoelectric properties and can be used in the preparation of organic optoelectronic devices, such as organic photodiodes (OLED) and photovoltaic cells.
3. curve structure: because of its special molecular structure, DBT can be used to build surface network structure and electronic structures.
Preparation Method:
DBT can be prepared in a variety of ways, common methods include:
1. Chemical synthesis: DBT is obtained by organic synthesis reaction, for example, reaction with anisole and acrolein, and then cyclization reaction.
2. Metal catalysis: DBT is obtained by coupling reaction of diphenyl imine and pyrrole acetal in the presence of a metal catalyst.
Safety Information:
1. DBT has no obvious harm to human health under ordinary operating conditions.
2. When handling DBT, follow routine laboratory practices, such as wearing personal protective equipment such as protective gloves, glasses, and laboratory coats.
3. DBT should be stored in a cool and dry place, and away from fire and oxidizing agents.
Last Update：2024-04-09 21:04:16
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