• 1. Evolution of shape, size, and areal density of a single plane of Si nanocrystals embedded in SiO2 matrix studied by atom probe tomography
  Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzene and substituted derivatives
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives
• Catalysts and Inorganic Chemicals Inorganic Compounds Oxides
• Catalysts and Inorganic Chemicals Inorganic Compounds Salt
• Catalysts and Inorganic Chemicals Inorganic Compounds

Chemical Profile of Tetraphenylarsonium chloride (CAS No. 507-28-8)

Tetraphenylarsonium chloride, identified by the Chemical Abstracts Service Number (CAS No.) 507-28-8, is a significant organoarsenic compound widely utilized in the field of synthetic chemistry and material science. This compound, characterized by its tetraphenylarsonium cation and chloride anion, has garnered attention for its unique structural properties and versatile applications in modern chemical research.

The molecular structure of Tetraphenylarsonium chloride consists of a central arsenic atom coordinated to four phenyl groups, forming a highly stable and symmetric tetrahedral arrangement. This configuration imparts exceptional electronic and steric properties, making it a valuable reagent in various chemical transformations. The presence of the phenyl groups enhances the compound's solubility in organic solvents, facilitating its use in solution-phase reactions and as a catalyst or intermediate in organic synthesis.

In recent years, Tetraphenylarsonium chloride has found applications in the development of advanced materials, particularly in the synthesis of liquid crystals and conductive polymers. Its ability to act as a template or dopant allows for the precise control of molecular alignment and electronic conductivity, which is crucial for the fabrication of next-generation electronic devices. Researchers have leveraged its stability under various conditions to create novel materials with enhanced performance characteristics.

Additionally, Tetraphenylarsonium chloride has been explored in the realm of pharmaceutical chemistry. Its unique reactivity enables the formation of complex organic architectures, which are essential for drug discovery and development. Studies have demonstrated its role in constructing heterocyclic compounds that exhibit promising biological activities. The compound's ability to facilitate cross-coupling reactions has made it a valuable tool in medicinal chemistry, particularly for generating novel pharmacophores with therapeutic potential.

Recent advancements in synthetic methodologies have expanded the utility of Tetraphenylarsonium chloride beyond traditional applications. For instance, it has been employed in asymmetric synthesis to achieve enantioselective transformations, contributing to the efficient production of chiral compounds. This capability is particularly relevant in the pharmaceutical industry, where enantiopure drugs are often required for optimal biological activity and minimal side effects.

The compound's stability under thermal and photochemical conditions has also been investigated extensively. Researchers have utilized Tetraphenylarsonium chloride as a stabilizer in polymerization reactions, enhancing the durability and performance of resulting materials. Its role as a photoacid generator has further intrigued scientists, as it can facilitate polymerization under controlled light exposure, enabling precise control over material properties.

In summary, Tetraphenylarsonium chloride (CAS No. 507-28-8) is a multifaceted compound with broad applications across synthetic chemistry, materials science, and pharmaceutical research. Its unique structural and electronic properties continue to drive innovation in these fields, making it an indispensable tool for researchers seeking to develop advanced materials and novel therapeutics.

• 603-32-7(Triphenylarsine)
• 15912-80-8(Arsonium, tetraphenyl-)
• 16242-55-0(Platinum,dichlorobis(triphenylarsine)-)
• 696-26-4(Arsine, dimethylphenyl-)
• 507-27-7(Tetraphenylarsonium bromide)
• 1499-33-8(Methyltriphenylarsonium iodide)
• 123334-18-9(TetraphenylarsoniuM Chloride Hydrochloride Hydrate)
• 14126-26-2(Palladium,dichlorobis(triphenylarsine)-)
• 14973-92-3(Chlorotris(triphenylarsine)rhodium)
• 104170-16-3(Tetraphenylarsonium chloride monohydrate)