Chemistry:Dimethylcadmium
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3D model (JSmol)
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| Properties | |
| C2H6Cd | |
| Molar mass | 142.484 g·mol−1 |
| Appearance | Colorless liquid |
| Odor | Foul; unpleasant; metallic; disagreeable; characteristic |
| Density | 1.985 g/mL |
| Melting point | −4.5 °C (23.9 °F; 268.6 K) |
| Boiling point | 106 °C (223 °F; 379 K) |
| Reacts with water | |
| Hazards | |
| Main hazards | Extremely toxic, reacts with water to release methane |
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| GHS Signal word | Danger |
| H225, H250, H252, H260, H301, H330, H350, H360 | |
| P101, P102, P103, P231, P222, P301+310, P303+361+353, P305+351+338, P403+233, P422, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | 18 °C (64 °F; 291 K) |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Dimethylcadmium is the organocadmium compound with the formula Cd(CH
3)
2. It is a colorless, highly toxic liquid that fumes in air. It is a linear molecule with C-Cd bond lengths of 213 pm.[1] The compound finds limited use as a reagent in organic synthesis and in metalorganic chemical vapor deposition (MOCVD). It has also been used in the synthesis of cadmium selenide nanoparticles, although efforts have been made to replace it in this capacity due to its toxicity.[2]
Dimethylcadmium is prepared by treating cadmium dihalides with methyl Grignard reagents or methyllithium.[3]
- CdBr
2 + 2 CH
3MgBr → Cd(CH
3)
2 + 2 MgBr
2
The same method was used in the first preparation of this compound.[4]
Dimethylcadmium is a weak Lewis acid, forming a labile adduct with diethyl ether. A yellow, air-sensitive adduct is formed with 2,2'-bipyridine.[3]
References
- ↑ Felix Hanke; Sarah Hindley; Anthony C. Jones; Alexander Steiner (2016). "The Solid State Structures of the High and Low Temperature Phases of Dimethylcadmium". Chemical Communications 52 (66): 10144–10146. doi:10.1039/c6cc05851e. PMID 27457504.
- ↑ Julia Hambrock; Alexander Birkner; Roland A. Fischer (2001). "Synthesis of CdSe nanoparticles using various organometallic cadmium precursors". Journal of Materials Chemistry 11 (12): 3197–3201. doi:10.1039/B104231A.
- ↑ 3.0 3.1 Douglas F. Foster; David J. Cole-Hamilton (1997). "Electronic Grade Alkyls of Group 12 and 13 Elements". Inorganic Syntheses. 31. pp. 21–66. doi:10.1002/9780470132623.ch7. ISBN 9780470132623.
- ↑ Erich Krause (1917). "Einfache Cadmiumdialkyle (I. Mitteilung über organische Cadmium-Verbindungen)". Berichte der deutschen chemischen Gesellschaft 50 (2): 1813–1822. doi:10.1002/cber.19170500292. https://zenodo.org/record/1426625.
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