Items 91 to 100 of 112 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Diphenyliodonium p-toluenesulfonate | 6293-66-9 | sc-396953 | 1 g | $114.00 | ||
Diphenyliodonium p-toluenesulfonate is a highly effective photoinitiator in electronic applications, known for its ability to generate cationic species upon UV irradiation. The presence of the p-toluenesulfonate group enhances its solubility in various solvents, promoting efficient light absorption and rapid initiation of polymerization processes. Its unique molecular structure allows for tailored reactivity, facilitating the formation of cross-linked networks essential for high-performance electronic materials. | ||||||
N-Hydroxynaphthalimide triflate | 85342-62-7 | sc-396955 | 1 g | $146.00 | ||
N-Hydroxynaphthalimide triflate serves as a versatile reagent in electronic applications, exhibiting remarkable electrophilic properties. Its triflate group enhances reactivity, enabling efficient nucleophilic substitutions and facilitating the formation of stable intermediates. The compound's unique naphthalimide moiety contributes to strong π-π stacking interactions, promoting effective charge transport in organic electronic devices. Additionally, its thermal stability and solubility in organic solvents make it ideal for various polymerization pathways, optimizing material performance. | ||||||
9,9′-Spirobifluorene | 159-66-0 | sc-396376 sc-396376A | 250 mg 1 g | $60.00 $80.00 | ||
9,9'-Spirobifluorene is a unique organic compound known for its exceptional charge transport properties in electronic applications. Its spiro structure allows for efficient π-π stacking, enhancing electron mobility and contributing to high-performance organic semiconductors. The compound exhibits strong photoluminescence, making it suitable for optoelectronic devices. Additionally, its robust thermal stability and low viscosity facilitate processing in thin-film applications, optimizing device efficiency. | ||||||
Allyltrimethoxysilane | 2551-83-9 | sc-239213 | 5 ml | $40.00 | ||
Allyltrimethoxysilane is a versatile silane compound that enhances adhesion and cross-linking in electronic materials. Its unique allyl group promotes radical polymerization, facilitating the formation of robust networks. The trimethoxysilane moiety enables effective bonding to various substrates, improving dielectric properties. This compound also exhibits hydrophobic characteristics, which can enhance moisture resistance in electronic applications, contributing to the longevity and reliability of devices. | ||||||
Lead(II) sulfide | 1314-87-0 | sc-397590 | 25 g | $70.00 | ||
Lead(II) sulfide is a semiconductor with notable photoconductive properties, making it valuable in optoelectronic applications. Its unique band structure allows for efficient charge carrier mobility, facilitating electron-hole pair generation under light exposure. The compound exhibits strong interactions with light, leading to significant changes in conductivity. Additionally, its high stability and low thermal conductivity make it suitable for use in infrared detectors and sensors, enhancing performance in electronic devices. | ||||||
m-Carborane | 16986-24-6 | sc-228425 | 1 g | $120.00 | ||
m-Carborane is a unique compound characterized by its robust three-dimensional structure, which enhances its thermal stability and resistance to chemical degradation. Its electron-rich nature allows for effective interactions with various substrates, facilitating charge transfer processes. The compound's distinctive cage-like geometry contributes to its low dielectric constant, making it an intriguing candidate for applications in high-performance electronic materials, particularly in insulating layers and as a filler in composites. | ||||||
Tri-p-tolylamine | 1159-53-1 | sc-396370 sc-396370A | 1 g 5 g | $40.00 $207.00 | ||
Tri-p-tolylamine exhibits remarkable electron-donating properties due to its aromatic amine structure, which enhances its conductivity in electronic applications. The compound's ability to form stable charge-transfer complexes with electron-accepting materials facilitates efficient energy transfer. Its high thermal stability and low volatility make it suitable for use in various electronic devices, where it can improve performance and reliability in conductive pathways and polymer matrices. | ||||||
2-(4-Methoxystyryl)-4,6-bis(trichloromethyl)-1,3,5-triazine | 42573-57-9 | sc-396959 | 5 g | $109.00 | ||
2-(4-Methoxystyryl)-4,6-bis(trichloromethyl)-1,3,5-triazine demonstrates unique electronic properties attributed to its triazine core, which allows for effective π-π stacking interactions. This compound exhibits strong electron-withdrawing characteristics due to the trichloromethyl groups, enhancing its role in charge transport mechanisms. Its robust thermal stability and ability to engage in diverse reaction pathways make it a promising candidate for advanced electronic materials, optimizing device efficiency and performance. | ||||||
Lithium sulfide | 12136-58-2 | sc-235518 sc-235518A | 5 g 10 g | $152.00 $270.00 | ||
Lithium sulfide is notable for its role in energy storage applications, particularly in lithium-ion batteries. Its ionic conductivity is enhanced by the presence of lithium ions, which facilitate rapid charge transport. The compound's ability to form stable sulfide networks allows for efficient lithium ion intercalation, optimizing battery performance. Additionally, its low density and high electrochemical stability contribute to improved cycle life and energy density in electronic devices. | ||||||
Tris(2,2′-bipyridine)dichlororuthenium(II) hexahydrate | 50525-27-4 | sc-253787 sc-253787A | 250 mg 1 g | $39.00 $95.00 | 1 | |
Tris(2,2'-bipyridine)dichlororuthenium(II) hexahydrate exhibits remarkable electronic characteristics due to its coordination complex structure. The bipyridine ligands facilitate strong π-π interactions, enhancing electron delocalization. This compound's unique redox properties enable efficient charge transfer, making it suitable for applications in electrochemical devices. Its stability in various environments and ability to participate in diverse electron transfer pathways further contribute to its potential in advanced electronic systems. | ||||||