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• 2. An alkynylboronatecycloaddition strategy to functionalised benzyne derivatives?
  James D. Kirkham,Patrick M. Delaney,George J. Ellames,Eleanor C. Row,Joseph P. A. Harrity Chem. Commun., 2010,46, 5154-5156
• 3. An integrated microfluidic platform for sensitive and rapid detection of biological toxins?
  Robert J. Meagher,Anson V. Hatch,Ronald F. Renzi,Anup K. Singh Lab Chip, 2008,8, 2046-2053
• 4. An assessment of strategies for the development of solid-state adsorbents for vehicular hydrogen storage
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• 5. Acetylcholinesterase amperometric detection system based on a cobalt(II) tetraphenylporphyrin-modified electrode
  Analyst, 1996,121, 1123-1126

• Solvents and Organic Chemicals Organic Compounds Phenylpropanoids and polyketides Diarylheptanoids Linear diarylheptanoids

Introduction to 1,3,5-Tris(4-Phenylphenyl)benzene (CAS No. 6326-64-3)

1,3,5-Tris(4-Phenylphenyl)benzene, also known by its CAS number 6326-64-3, is a high-performance organic compound that has garnered significant attention in the fields of materials science and organic chemistry. This compound is characterized by its unique molecular structure, which consists of a central benzene ring substituted with three 4-phenylphenyl groups. The symmetrical and rigid nature of this molecule makes it an excellent candidate for various applications, particularly in the development of advanced materials and optoelectronic devices.

The molecular formula of 1,3,5-Tris(4-Phenylphenyl)benzene is C₃₇H₂₈, and its molecular weight is approximately 480.62 g/mol. The compound exhibits excellent thermal stability and a high glass transition temperature (Tg), which are crucial properties for its use in high-performance polymers and coatings. These characteristics make it a valuable component in the formulation of materials that require robust mechanical and thermal properties.

Recent research has highlighted the potential of 1,3,5-Tris(4-Phenylphenyl)benzene in the development of organic light-emitting diodes (OLEDs). OLEDs are widely used in display technologies due to their high efficiency, low power consumption, and excellent color quality. The unique electronic properties of 1,3,5-Tris(4-Phenylphenyl)benzene, including its high electron mobility and excellent hole transport capabilities, make it an ideal material for enhancing the performance of OLEDs. Studies have shown that incorporating this compound into OLED structures can significantly improve device efficiency and stability.

In addition to its applications in OLEDs, 1,3,5-Tris(4-Phenylphenyl)benzene has also been explored for use in organic photovoltaic (OPV) cells. OPVs are a promising technology for renewable energy generation due to their lightweight and flexible nature. The compound's ability to absorb light efficiently across a broad spectrum makes it a suitable candidate for improving the power conversion efficiency of OPVs. Recent advancements in the synthesis and characterization of 1,3,5-Tris(4-Phenylphenyl)benzene-based materials have paved the way for more efficient and cost-effective OPV devices.

The synthesis of 1,3,5-Tris(4-Phenylphenyl)benzene typically involves multi-step reactions, including Suzuki coupling and Friedel-Crafts alkylation. These reactions require precise control over reaction conditions to ensure high yields and purity. Advances in catalytic methods have significantly improved the efficiency and scalability of these synthetic processes. For instance, the use of palladium-based catalysts has been shown to enhance the yield and selectivity of the Suzuki coupling reaction, making it more feasible for large-scale production.

The physical properties of 1,3,5-Tris(4-Phenylphenyl)benzene, such as its melting point (approximately 270°C), solubility in common organic solvents like toluene and chloroform, and its crystalline structure, have been extensively studied. These properties are crucial for optimizing its performance in various applications. For example, the high melting point and crystallinity contribute to its stability under harsh conditions, making it suitable for use in high-temperature environments.

Beyond its applications in electronics and materials science, 1,3,5-Tris(4-Phenylphenyl)benzene has also been investigated for its potential biological activities. Preliminary studies have suggested that this compound may exhibit anti-inflammatory properties due to its ability to modulate certain signaling pathways involved in inflammation. While more research is needed to fully understand its biological effects, these findings open up new avenues for exploring its use in pharmaceuticals.

In conclusion, 1,3,5-Tris(4-Phenylphenyl)benzene (CAS No. 6326-64-3) is a versatile organic compound with a wide range of applications in advanced materials and optoelectronic devices. Its unique molecular structure and excellent physical properties make it an attractive candidate for various industrial and scientific uses. Ongoing research continues to uncover new potential applications and improve our understanding of this fascinating compound.

• 92-06-8(M-Terphenyl)
• 3073-05-0(p-Quinquephenyl)
• 25570-02-9(3,3',5,5'-Tetramethylbiphenyl)
• 1166-18-3(m,m-Quaterphenyl)
• 4499-83-6(p-Sexiphenylene)
• 1594-86-1(BIPHENYL-UL-14C)
• 17057-88-4(3,5-Dimethyl-biphenyl (>85%))
• 16716-13-5(1,1':3',1'':3'',1''':3''',1''''-Quinquephenyl)
• 15039-46-0(1,1':3',1'':3'',1''':4''',1'''':3'''',1'''''-Sexiphenyl(6CI,7CI,8CI,9CI))
• 17714-84-0(m-Terphenyl-d14)