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Dimethylcadmium

From Wikipedia, the free encyclopedia
Dimethylcadmium
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard100.007.324Edit this at Wikidata
EC Number
  • 208-055-4
UNII
  • InChI=1S/2CH3.Cd/h2*1H3;
    Key: KVVGSXJGEUULNM-UHFFFAOYSA-N
  • C[Cd]C
Properties
C2H6Cd
Molar mass142.484 g·mol−1
AppearanceColorless liquid
OdorFoul; unpleasant; metallic; disagreeable; characteristic
Density1.985 g/mL
Melting point−4.5 °C (23.9 °F; 268.6 K)
Boiling point106 °C (223 °F; 379 K)
Reacts with water
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Extremely toxic, reacts with water to releasemethane
GHS labelling:
GHS02: FlammableGHS06: ToxicGHS08: Health hazard
Danger
H225,H250,H252,H260,H301,H330,H350,H360
P101,P102,P103,P222,P231,P301+P310,P303+P361+P353,P305+P351+P338,P403+P233,P422,P501
NFPA 704 (fire diamond)
Flash point18 °C (64 °F; 291 K)
Related compounds
Related compounds
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Dimethylcadmium is theorganocadmium compound with the formulaCd(CH3)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 inorganic synthesis and inmetalorganic chemical vapor deposition (MOCVD). It has also been used in the synthesis ofcadmium 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 methylGrignard reagents ormethyllithium.[3]

CdBr2 + 2 CH3MgBr → Cd(CH3)2 + 2 MgBr2

The same method was used in the first preparation of this compound.[4]

Dimethylcadmium is a weakLewis acid, forming a labile adduct withdiethyl ether. A yellow, air-sensitive adduct is formed with2,2'-bipyridine.[3]

References

[edit]
  1. ^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.
  2. ^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. ^abDouglas F. Foster; David J. Cole-Hamilton (1997). "Electronic Grade Alkyls of Group 12 and 13 Elements".Inorganic Syntheses. Vol. 31. pp. 21–66.doi:10.1002/9780470132623.ch7.ISBN 9780470132623.
  4. ^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.
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