Items 11 to 20 of 38 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Triphenylborane - Triphenylphosphine Complex | 3053-68-7 | sc-296642 sc-296642A | 5 g 25 g | $110.00 $295.00 | ||
Triphenylborane - Triphenylphosphine Complex serves as a versatile phosphine ligand characterized by its strong π-acceptor capabilities and significant steric hindrance. The presence of three phenyl groups allows for effective π-backbonding with transition metals, enhancing electronic interactions. This complex exhibits unique coordination geometries, influencing the stability and reactivity of metal complexes. Its ability to modulate electronic properties makes it a key player in various catalytic pathways, impacting reaction dynamics and selectivity. | ||||||
1,3-Bis(diphenylphosphino)propane | 6737-42-4 | sc-222926 sc-222926A sc-222926B sc-222926C sc-222926D | 1 g 5 g 100 g 500 g 1 kg | $26.00 $46.00 $82.00 $271.00 $437.00 | ||
1,3-Bis(diphenylphosphino)propane is a bidentate phosphine ligand known for its chelating ability, which enhances metal coordination through dual phosphorus donor sites. This ligand exhibits remarkable steric bulk due to its diphenyl groups, influencing the geometry of metal complexes and promoting unique reactivity patterns. Its electron-donating properties facilitate strong metal-ligand interactions, significantly affecting catalytic efficiency and selectivity in various reactions. | ||||||
1,2-Bis(diphenylphosphino)benzene | 13991-08-7 | sc-222795 | 1 g | $71.00 | ||
1,2-Bis(diphenylphosphino)benzene is a versatile bidentate phosphine ligand characterized by its rigid, planar structure, which allows for effective coordination with transition metals. The presence of two diphenylphosphino groups enhances its ability to stabilize low oxidation states of metals, promoting unique electronic environments. This ligand's steric and electronic properties can significantly influence reaction pathways, enhancing selectivity and reactivity in catalytic processes. | ||||||
1,6-Bis(diphenylphosphino)hexane | 19845-69-3 | sc-223099 | 5 g | $106.00 | ||
1,6-Bis(diphenylphosphino)hexane is a flexible bidentate phosphine ligand notable for its ability to form stable chelate complexes with transition metals. Its extended aliphatic chain provides a unique spatial arrangement, facilitating diverse coordination geometries. This ligand's steric bulk and electronic characteristics can modulate metal reactivity, influencing catalytic efficiency and selectivity in various reactions, particularly in cross-coupling and hydrogenation processes. | ||||||
1,2-Bis(dicyclohexylphosphino)ethane | 23743-26-2 | sc-222793 sc-222793A | 1 g 5 g | $101.00 $398.00 | ||
1,2-Bis(dicyclohexylphosphino)ethane is a versatile bidentate phosphine ligand characterized by its robust steric hindrance and unique electronic properties. The dicyclohexyl groups enhance its ability to stabilize low-valent metal complexes, promoting distinct coordination modes. This ligand's structural rigidity allows for effective metal-ligand interactions, influencing reaction pathways and kinetics in catalytic processes, particularly in asymmetric synthesis and organometallic transformations. | ||||||
1,2-Bis(dichlorophosphino)ethane | 28240-69-9 | sc-222792 sc-222792A | 1 g 5 g | $75.00 $219.00 | ||
1,2-Bis(dichlorophosphino)ethane is a bidentate phosphine ligand notable for its strong electron-withdrawing dichlorophosphino groups, which enhance its ability to stabilize transition metal complexes. This ligand exhibits unique coordination geometries, facilitating diverse metal-ligand interactions. Its distinct electronic characteristics can significantly influence reaction kinetics and selectivity in catalytic cycles, making it a key player in various organometallic reactions and catalysis. | ||||||
1,4-Bis(dicyclohexylphosphino)butane | 65038-36-0 | sc-223015 | 1 g | $128.00 | ||
1,4-Bis(dicyclohexylphosphino)butane is a versatile bidentate phosphine ligand characterized by its bulky dicyclohexyl groups, which provide steric hindrance and enhance metal-ligand interactions. This ligand promotes unique coordination modes, allowing for the stabilization of low-valent transition metal complexes. Its electron-donating properties can modulate the electronic environment of the metal center, influencing catalytic activity and selectivity in various organometallic transformations. | ||||||
1,2-Bis[bis(pentafluorophenyl)phosphino]ethane | 76858-94-1 | sc-222810 | 1 g | $204.00 | ||
1,2-Bis[bis(pentafluorophenyl)phosphino]ethane is a highly specialized bidentate phosphine ligand known for its exceptional electron-withdrawing pentafluorophenyl groups. This unique structure enhances metal coordination by stabilizing high oxidation states and facilitating strong π-acceptor interactions. Its distinctive steric and electronic properties enable fine-tuning of reaction kinetics, making it effective in promoting selectivity and reactivity in organometallic catalysis. | ||||||
1,3-Bis(diphenylphosphino)propane monooxide | 85685-99-0 | sc-222927 | 5 g | $286.00 | ||
1,3-Bis(diphenylphosphino)propane monooxide is a versatile bidentate phosphine ligand characterized by its ability to form stable complexes with transition metals. The presence of the monooxide group introduces unique electronic effects, enhancing the ligand's donor properties. This compound exhibits remarkable steric hindrance, which influences the geometry of metal complexes, thereby modulating catalytic pathways and improving selectivity in various reactions. Its distinct interactions with metal centers facilitate the activation of substrates, making it a key player in organometallic chemistry. | ||||||
1-Diphenylphosphino-1′-(di-tert-butylphosphino)ferrocene | 95408-38-1 | sc-222690 | 1 g | $134.00 | ||
1-Diphenylphosphino-1'-(di-tert-butylphosphino)ferrocene is a versatile phosphine ligand characterized by its unique ferrocene backbone, which imparts significant stability and electronic properties. The sterically demanding di-tert-butylphosphino groups enhance its ability to stabilize metal centers, promoting favorable coordination geometries. This ligand exhibits remarkable electronic communication between the metal and the ferrocene unit, influencing catalytic activity and selectivity in various reactions. Its distinct steric and electronic features enable tailored interactions with transition metals, facilitating innovative pathways in organometallic chemistry. | ||||||