Xantphos
Chemical compound
From Wikipedia, the free encyclopedia
Xantphos is an organophosphorus compound derived from the heterocycle xanthene. It is used as a bidentate diphosphine ligand and is noteworthy for having a particularly wide bite angle (108°).[1] Such ligands are useful in the hydroformylation of alkenes.[2] Illustrative of its wide bite angle, it forms both cis and trans adducts of platinum(II) chloride. In the latter context, xantphos is classified as a trans-spanning ligand. A related bidentate ligand with a greater bite angle is spanphos.
Ph stands for phenyl | |
| Names | |
|---|---|
| Preferred IUPAC name
(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphane) | |
| Other names
Xantphos | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.118.008 |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C39H32OP2 | |
| Molar mass | 578.62 g/mol |
| Appearance | colorless solid |
| Density | 1.34 g/mL |
| Melting point | 224 to 228 °C (435 to 442 °F; 497 to 501 K) |
| organic solvents | |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards |
flammable |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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The ligand is prepared by double directed lithiation of 9,9-dimethylxanthene with sec-butyllithium followed by treatment with chlorodiphenylphosphine.[3]

