Difference between revisions of "1,2-Bis(dimethylarsino)benzene"
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Latest revision as of 19:15, 21 September 2010
| 1,2-Bis(dimethylarsino)benzene | |
|---|---|
| File:Diars.png | |
| 1,2-Bis(dimethylarsino)benzene | |
| Other names diars
o-Phenylenebis(dimethylarsine) DAS | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| CAS number | 13246-32-7 |
| ChemSpider | 75125 |
| SMILES | Script error: No such module "collapsible list". |
| InChI | Script error: No such module "collapsible list". |
| InChI key | HUBWRAMPQVYBRS-UHFFFAOYAM |
| style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
| Molecular formula | C10H16As2 |
| Molar mass | 286.08 |
| Appearance | colourless liquid |
| Density | 1.3992 g/cm3 |
| Boiling point |
97-101 °C (1.1 mm Hg) |
| style="background: #F8EABA; text-align: center;" colspan="2" | Hazards | |
| Main hazards | toxic |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
1,2-Bis(dimethylarsino)benzene is the organoarsenic compound with the formula C6H4(As(CH3)2)2. The molecule consists of two dimethylarsino groups attached to adjacent carbon centers of a benzene ring. It is a chelating ligand in coordination chemistry. This colourless oil is popularly abbreviated "diars."[1] Related, but non-chelating organoarsenic ligands include triphenylarsine and trimethylarsine. Work on diars led to the development of the chelating diphosphine ligands such as dppe, which are now prevalent in homogeneous catalysis.
Coordination chemistry
Diars is a bidentate ligand used in coordination chemistry. It was first described in 1939,[2] but was popularlized by R. S. Nyholm for its ability to stabilize metal complexes with unusual oxidation states and coordination numbers, e.g. TiCl4(diars)2. High coordination numbers arise because diars is fairly compact and the As-M bonds are long, which relieves crowding at the metal center. In terms of stabilizing unusual oxidation states, diars stabilizes Ni(III), as in [NiCl2(diars)2]Cl.
Of historical interest is the supposedly diamagnetic [Ni(diars)3](ClO4)2, obtained by heating nickel perchlorate with diars. Octahedral d8 complexes characteristically have triplet ground states, so the diamagnetism of this complex was puzzling. Later by X-ray crystallography, the complex was shown to be pentacoordinate with the formula [Ni(triars)(diars)](ClO4)2, where triars is the tridentate ligand [C6H4As(CH3]2As(CH3), arising from the elimination of trimethylarsine.[3][4]
Preparation and handling
Diars is prepared by the reaction of ortho-dichlorobenzene and sodium dimethylarsenide:[5]
- C6H4Cl2 + 2 NaAs(CH3)2 → C6H4(As(CH3)2)2 + 2 NaCl
It is a colorless liquid. Oxygen quickly converts diars to the dioxide, C6H4(As(CH3)2O)2.
References
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<references />, or <references group="..." />- ↑ Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5.
- ↑ Chatt, J.; Mann, F. G. "The Synthesis of Ditertiary Arsines. Meso- and Racemic Forms of Bis-4-Covalent-Arsenic Compounds" Journal of the Chemical Society, 1939, 610–615. doi:10.1039/JR9390000610
- ↑ B. Bosnich, R. S. Nyholm, P. J. Pauling, M. L. Tobe "A nickel(II)-catalyzed synthesis of a triarsine from a diarsine" J. Am. Chem. Soc. 1968, volume 90, pp 4741–4742. doi:10.1021/ja01019a049
- ↑ Anthony Nicholl Rail; Some new reactions of a ditertiary arsine ligand; Ph.D. Thesis; University College London; 1973
- ↑ Feltham, R. D.; Silverthorn, W. "o-Phenylenebis(dimethylarsine)" Inorganic Syntheses 1967, volume X, 159–164.
