54842-92-1

Basic information

• Product Name: Anthracene, 9,10-bis(4-ethenylphenyl)-
• CAS NO: 54842-92-1
• Molecular Formula: C30H22
• Molecular Weight: 382.505
• Mol File: 54842-92-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Anthracene, 9,10-bis(4-ethenylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Anthracene, 9,10-bis(4-ethenylphenyl)-(54842-92-1)
• EPA Substance Registry System: Anthracene, 9,10-bis(4-ethenylphenyl)-(54842-92-1)

Safety Data

• Hazardous Substances Data: 54842-92-1(Hazardous Substances Data)

Upstream product

• 523-27-3 9,10-Dibromoanthracene 
• 2156-04-9 4-Vinylphenylboronic acid 

Downstream Products

• 1041774-04-2 9,10-bis(4-(2-(3-chloropropylthio)ethyl)phenyl)anthracene 
• 1606988-72-0 9,10-bis(4-((E)-2-(trimethylsilyl)vinyl)phenyl)anthracene 
• 1016987-16-8 C₅₂H₄₄N₂S₄ 

Relevant articles and documents

Unusual: Cis and trans architecture of dihydrofunctional double-decker shaped silsesquioxane and synthesis of its ethyl bridged π-conjugated arene derivatives

Double-decker silsesquioxanes have gained a high reputation in many branches of chemistry and process development. In particular, catalytic processes that convert double-decker silsesquioxanes into important functional classes of fine chemicals are a central topic of contemporary organosilicon chemistry. Although the 9,19-di(hydro)octaphenyl double-decker silsesquioxane (DDSQ-2SiH) is known, we report its cis and trans structure and X-ray structure for the first time. The combination of DDSQ-2SiH in a known hydrosilylation reaction protocol with precise reaction time control (FT-IR in situ apparatus) allowed us to selectively assemble a series of previously unreported molecular double-decker silsesquioxanes with ethyl bridged π-conjugated arenes. These compounds were used as a molecular model to obtain their respective macromolecular hybrid analogues. The obtained compounds were characterized spectroscopically and their thermal parameters were also verified.

Synthesis and properties of chromophore-functionalized monovinylsilsesquioxane derivatives

A facile and efficient Pd-based Suzuki-Miyaura coupling reaction leading to mixed chromophores with styryl fragments, enabling their further application, is presented. We also disclose their use in the formation of monofunctionalized silsesquioxanes with a chromophore group covalently bound to a T8 core that have been prepared via a cross-metathesis reaction. These new materials were studied in terms of their photophysical and also thermal properties.

Controlled release of singlet oxygen using diphenylanthracene functionalized polymer nanoparticles

Functionalized polymer nanoparticles react and store molecular oxygen for several weeks in the form of endoperoxides. On-demand controlled release of singlet oxygen by the particles is achieved by thermolysis. The Royal Society of Chemistry 2014.