Items 41 to 50 of 112 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Molybdenum(IV) selenide | 12058-18-3 | sc-269613 | 5 g | $126.00 | ||
Molybdenum(IV) selenide is a notable material in electronics, characterized by its layered structure that allows for efficient charge transport. Its unique electronic properties arise from strong covalent bonding and the presence of d-electrons, which contribute to its semiconducting behavior. The compound exhibits high mobility of charge carriers, making it suitable for applications in field-effect transistors and photodetectors, where rapid response times are essential. | ||||||
D-102 Dye | 652145-28-3 | sc-214799 | 1 mg | $460.00 | ||
D-102 Dye is an innovative compound in electronics, distinguished by its vibrant color and ability to absorb specific wavelengths of light. Its unique molecular structure facilitates strong π-π stacking interactions, enhancing charge transfer efficiency. The dye exhibits remarkable photostability and tunable electronic properties, making it ideal for applications in organic light-emitting diodes (OLEDs) and solar cells, where efficient light absorption and emission are critical. | ||||||
4-Ethynyl-α,α,α-trifluorotoluene | 705-31-7 | sc-254660 | 5 g | $199.00 | ||
4-Ethynyl-α,α,α-trifluorotoluene is a notable compound in electronics, characterized by its unique trifluoromethyl group that enhances electron-withdrawing properties. This feature promotes strong dipole interactions, improving the stability of charge carriers. Its distinct alkyne functionality allows for versatile coupling reactions, facilitating the formation of complex electronic materials. Additionally, its low dielectric constant contributes to reduced signal loss in high-frequency applications, making it suitable for advanced electronic devices. | ||||||
1,5-Pentanedithiol | 928-98-3 | sc-237785 | 5 g | $57.00 | ||
1,5-Pentanedithiol is a versatile compound in electronics, notable for its ability to form robust thiol-based linkages. These linkages enhance molecular conductivity and facilitate charge transfer, making it ideal for creating stable interfaces in electronic components. Its unique bifunctional structure allows for effective self-assembly and integration into nanostructured materials, promoting enhanced electron mobility. Additionally, its strong affinity for metal surfaces aids in the development of reliable electronic contacts. | ||||||
1,4-Butanedithiol | 1191-08-8 | sc-253987 | 5 g | $106.00 | ||
1,4-Butanedithiol is a significant compound in electronics, characterized by its ability to form strong dithiol bonds that enhance molecular stability and conductivity. Its symmetrical structure promotes effective self-assembly, allowing for the creation of organized nanostructures. The compound's reactivity with metal surfaces facilitates the formation of reliable junctions, while its unique electronic properties contribute to improved charge transport in various electronic applications. | ||||||
1,6-Hexanedithiol | 1191-43-1 | sc-280254 | 5 g | $46.00 | ||
1,6-Hexanedithiol is a versatile compound in electronics, notable for its long-chain structure that enables enhanced flexibility and molecular alignment. Its terminal thiol groups engage in robust interactions with metal substrates, promoting effective adhesion and stability in electronic devices. The compound's ability to form self-assembled monolayers aids in tailoring surface properties, while its unique electron-donating characteristics improve charge transfer efficiency, making it ideal for advanced electronic applications. | ||||||
1,8-Octanedithiol | 1191-62-4 | sc-396714 | 1 g | $41.00 | ||
1,8-Octanedithiol is a significant compound in electronics, characterized by its extended carbon chain that facilitates unique molecular packing and orientation. The two thiol groups at each end enable strong coordination with metal surfaces, enhancing interfacial properties. Its capacity to form stable self-assembled monolayers allows for precise control over surface chemistry, while its distinct electron-rich nature contributes to improved conductivity and charge transport in electronic systems. | ||||||
1-Heptanethiol | 1639-09-4 | sc-224687 | 25 g | $66.00 | ||
1-Heptanethiol plays a pivotal role in electronics due to its unique structural properties, featuring a terminal thiol group that promotes strong interactions with metal substrates. This compound can form robust self-assembled monolayers, which enhance surface uniformity and stability. Its hydrophobic carbon chain aids in reducing surface energy, while the thiol functionality facilitates effective charge transfer, making it essential for optimizing electronic device performance. | ||||||
n-Tetradecyl mercaptan | 2079-95-0 | sc-269896 | 5 g | $58.00 | ||
n-Tetradecyl mercaptan is significant in electronics for its long hydrophobic carbon chain, which enhances surface adhesion and stability on conductive materials. The terminal thiol group enables the formation of self-assembled monolayers, promoting uniformity and reducing interfacial resistance. Its unique molecular interactions facilitate effective electron transfer, while the extended alkyl chain contributes to the overall dielectric properties, optimizing performance in various electronic applications. | ||||||
1,9-Nonanedithiol | 3489-28-9 | sc-265109 | 1 g | $58.00 | ||
1,9-Nonanedithiol is notable in electronics for its unique bifunctional structure, featuring two thiol groups that enable robust cross-linking and enhanced molecular interactions. This dual thiol functionality promotes the formation of stable networks on surfaces, improving adhesion and conductivity. Its ability to form strong bonds with metal substrates enhances charge transport efficiency, while its flexible chain contributes to tunable dielectric properties, making it ideal for advanced electronic applications. | ||||||