Diphenyl ditelluride
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| Names | |
|---|---|
|  IUPAC name
 Diphenylditelluide  | |
|  Other names
 Phenylditelluride  | |
| Identifiers | |
|  32294-60-3  | |
| ChemSpider |  90943  | 
| Jmol interactive 3D |  Image Image  | 
| PubChem | 100657 | 
 
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| Properties | |
| C12H10Te2 | |
| Molar mass | 409.42 g/mol | 
| Appearance | Orange powder | 
| Density | 2.23 g/cm3 | 
| Melting point | 66 to 67 °C (151 to 153 °F; 339 to 340 K) | 
| Boiling point | decomposes | 
| Insoluble | |
| Solubility in other solvents | Dichloromethane | 
| Structure | |
|  90° at Se C2 symmetry  | |
| 0 D | |
| Hazards | |
| Main hazards | Toxic | 
| R-phrases | 20/21/22-36/37/38 | 
| S-phrases | 26-36 | 
| Related compounds | |
|   Related compounds  | 
 Ph2S2, Ph2Se2  | 
|   Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).  | |
|   | |
| Infobox references | |
Diphenylditelluride is the chemical compound with the formula (C6H5Te)2, abbreviated Ph2Te2 This orange-coloured solid is the oxidized derivative of the unstable benzenetellurol, PhTeH. Ph2Te2 is used as a source of the PhTe unit in organic synthesis.
Preparation
Ph2Te2 is prepared by the oxidation of tellurophenolate, which is generated via the Grignard reagent:[1]
- PhMgBr + Te → PhTeMgBr
 - 2PhTeMgBr + 0.5 O2 + H2O → Ph2Te2 + 2 MgBr(OH)
 
The molecule has C2 symmetry.
References
- ↑ Crich, D.; Yao, Q. "Diphenyl Ditelluride" in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. doi:10.1002/047084289.
 
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