Interesting facts
Interesting Facts about Naphtho[2,3-b]benzothiophene
Naphtho[2,3-b]benzothiophene is a fascinating compound that belongs to a class of polycyclic aromatic compounds. This compound is particularly noteworthy for its unique structure and properties.
Structural Characteristics
- Polycyclic Structure: It consists of fused aromatic rings, which contribute to its interesting electronic properties.
- Sulfur Incorporation: The presence of a thiophene unit in its structure provides unique reactivity and electronic characteristics.
Applications and Uses
This compound has garnered attention in various fields:
- Organic Electronics: Naphtho[2,3-b]benzothiophene is studied for its potential use in organic semiconductors and photovoltaic devices.
- Material Science: Its properties make it suitable for creating materials with specific optical and electronic behaviors.
Research Insights
Ongoing research into naphtho[2,3-b]benzothiophene is uncovering more of its capabilities:
- Researchers are exploring its ability to act as a donor material in organic solar cells.
- Studies are focused on understanding its interaction with other compounds, which may lead to innovative applications in drug delivery systems.
Overall, naphtho[2,3-b]benzothiophene exemplifies how a complex molecular structure can bridge the gap between chemistry and practical applications, showcasing the significance of polycyclic aromatic compounds in modern science.
Synonyms
Benzo[b]naphtho[2,3-d]thiophene
243-46-9
BENZO(B)NAPHTHO(2,3-D)THIOPHENE
naphtho[2,3-b][1]benzothiole
Benzonaphthothiophene
EINECS 205-956-4
61523-34-0
Naphtho[2,3-b][1]benzothiophene
H53JV5C3NA
SCHEMBL2742087
DTXSID5075442
Naphtho[3,2-b][1]benzothiole
2,3-BNT
Naphtho[2,3-b][1]benzothiophene #
DB-244266
NS00027630
G91274
BENZO (b) NAPHTHO (2,3-d) THIOPHENE (purity)
Benzo[b]naphtho[2,3-d]thiophene, BCR(R) certified Reference Material
205-956-4
Solubility of Naphtho[2,3-b]benzothiophene
Naphtho[2,3-b]benzothiophene is a fascinating compound when it comes to its solubility characteristics. This polycyclic aromatic compound exhibits notable insolubility in water, which is a common trait among many organic compounds that feature extensive aromatic structures. The factors contributing to its limited aqueous solubility include:
In contrast, naphtho[2,3-b]benzothiophene may be more soluble in organic solvents, particularly those that can interact through π-π stacking or other non-polar interactions. For example:
In summary, the solubility of naphtho[2,3-b]benzothiophene is *substantially limited in polar solvents like water* but shows a propensity for solubility in non-polar organic solvents. This characteristic is essential to consider for applications in organic electronics and materials science, where solubility affects processing and performance.