Names | |
---|---|
IUPAC name
Diphenylditelluide
|
|
Other names
Phenylditelluride
|
|
Identifiers | |
3D model (JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.046.332 |
PubChem CID
|
|
|
|
|
|
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R-phrases (outdated) | 20/21/22-36/37/38 |
S-phrases (outdated) | 26-36 |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).
|
|
what is ?) | (|
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.
Ph2Te2 is prepared by the oxidation of tellurophenolate, which is generated via the Grignard reagent:
The molecule has C2 symmetry.