Diphenyl diselenide
| |
| |
| Names | |
|---|---|
| IUPAC name
1,1′-Diselanediyldibenzene
| |
| Other names
Phenyl diselenide
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
| ECHA InfoCard | 100.015.256 |
| EC Number |
|
PubChem CID
|
|
| RTECS number |
|
| UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
| Properties | |
| C12H10Se2 | |
| Molar mass | 312.154 g·mol−1 |
| Appearance | Yellow crystals |
| Density | 1.84 g/cm3 |
| Melting point | 59 to 61 °C (138 to 142 °F; 332 to 334 K) |
| Insoluble | |
| Solubility in other solvents | Dichloromethane, THF, hot Hexane |
| Structure | |
| 90° at Se[citation needed] C2 symmetry[citation needed] | |
| 0 D | |
| Hazards | |
| GHS labelling: | |
  
| |
| Danger | |
| H301, H331, H373, H410 | |
| P260, P261, P264, P270, P271, P273, P301+P310, P304+P340, P311, P314, P321, P330, P391, P403+P233, P405, P501 | |
| Related compounds | |
Related compounds
|
Ph2S2, C6H5SeH |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Diphenyl diselenide is the chemical compound with the formula (C6H5)2Se2, abbreviated Ph2Se2. This yellow-coloured solid is the oxidized derivative of benzeneselenol. It is used as a source of the PhSe unit in organic synthesis.
Preparation and properties
[edit]Ph2Se2 is prepared by the oxidation of benzeneselenoate, the conjugate base of benzeneselenol which is generated via the Grignard reagent:[1]
The molecule has idealized C2-symmetry, like hydrogen peroxide and related molecules. The Se-Se bond length of 2.29 Å the C-Se-Se-C dihedral angle is 82° and the C-Se-Se angles are near 110°.[2]
Medical applications
[edit]Diphenyl diselenide alleviates methylmercury poisoning in grass carp.[3]
Reactions
[edit]A reaction characteristic of Ph2Se2 is its reduction:
- Ph2Se2 + 2 Na → 2 PhSeNa
PhSeNa is a useful nucleophile used to introduce the phenylselenyl group by nucleophilic substitution of alkyl halides, alkyl sulfonates (mesylates or tosylates) and epoxides. The example below was taken from a synthesis of morphine.[4]
Another characteristic reaction is chlorination:
- Ph2Se2 + Cl2 → 2 PhSeCl
PhSeCl is a powerful electrophile, used to introduce PhSe groups by reaction with a variety of nucleophiles, including enolates, enol silyl ethers, Grignard reagents, organolithium reagents, alkenes and amines. In the sequence below (early steps in the synthesis of Strychnofoline), a PhSe group is introduced by reaction of a lactam enolate with PhSeCl.[5] This sequence is a powerful method for the conversion of carbonyl compounds to their α,β-unsaturated analogs.[6]
Diphenyl diselenide itself is also a source of a weakly electrophilic PhSe group in reactions with relatively powerful nucleophiles like Grignard reagents, lithium reagents and ester enolates (but not ketone enolates or weaker nucleophiles). PhSeCl is both more reactive, and more efficient, since with Ph2Se2 half of the selenium is wasted.
- Ph2Se2 + Nu− → PhSeNu + PhSe−
N-Phenylselenophthalimide (N-PSP) can be used if PhSeCl is too strong and diphenyl diselenide is too weak or wasteful.[7]
References
[edit]- ^ Reich, H. J.; Cohen, M. L.; Clark, P. S. (1979). "Reagents for Synthesis of Organoselenium Compounds: Diphenyl Diselenide and Benzeneselenenyl Chloride". Organic Syntheses. 59: 141; Collected Volumes, vol. 6, p. 533.
- ^ Marsh, R. E. (1952). "The Crystal Structure of Diphenyl Diselenide". Acta Crystallographica. 5 (4): 458–462. doi:10.1107/S0365110X52001349.
- ^ Baldissera, Matheus D.; Souza, Carine F.; da Silva, Aleksandro S.; Henn, Alessandra S.; Flores, Erico M. M.; Baldisserotto, Bernardo (2020). "Diphenyl diselenide dietary supplementation alleviates behavior impairment and brain damage in grass carp (Ctenopharyngodon idella) exposed to methylmercury chloride". Comparative Biochemistry and Physiology. Toxicology & Pharmacology. 229: 108674. doi:10.1016/j.cbpc.2019.108674. ISSN 1532-0456. PMID 31760078. S2CID 208274623.
- ^ Taber, D. F.; Neubert, T. D.; Rheingold, A. L. (2002). "Synthesis of (−)-Morphine". Journal of the American Chemical Society. 124 (42): 12416–12417. doi:10.1021/ja027882h. PMID 12381175.
- ^ Lerchner, A.; Carreira, E. M. (2002). "First Total Synthesis of (±)-Strychnofoline via a Highly Selective Ring-Expansion Reaction". Journal of the American Chemical Society. 124 (50): 14826–14827. doi:10.1021/ja027906k. PMID 12475306.
- ^ Reich, H. J.; Wollowitz, S. (1993). "Preparation of α,β-Unsaturated Carbonyl Compounds and Nitriles by Selenoxide Elimination". Organic Reactions. 44: 1–296. doi:10.1002/0471264180.or044.01. ISBN 0471264180.
- ^ Barrero, A. F.; Alvarez-Manzaneda, E. J.; Chahboun, R.; Corttés, M.; Armstrong, V. (1999). "Synthesis and Antitumor Activity of Puupehedione and Related Compounds". Tetrahedron. 55 (52): 15181–15208. doi:10.1016/S0040-4020(99)00992-8.