Organogallium chemistry

Organogallium chemistry is the chemistry of organometallic compounds containing a carbon to gallium (Ga) chemical bond. Despite their high toxicity, organogallium compounds have some use in organic synthesis. The compound trimethylgallium is of some relevance to MOCVD as a precursor to gallium arsenide via its reaction with arsine at 700 °C:

Ga(CH3)3 + AsH3 → GaAs + 3CH4

Gallium trichloride is an important reagent for the introduction of gallium into organic compounds.

The main gallium oxidation state is Ga(III), as in all lower group 13 elements (such as aluminium).[1][2]

Organogallium(III) chemistry

Compounds of the type R3Ga are monomeric. Lewis acidity decreases in the order Al > Ga > In and as a result organogallium compounds do not form bridged dimers as organoaluminum compounds do. Organogallium compounds are also less reactive than organoaluminum compounds. They do form stable peroxides.[3]

Organogallium compounds can be synthesized by transmetallation, for example the reaction of gallium metal with dimethylmercury:

2Ga + 3Me2Hg → 2Me3Ga + 3 Hg

or via organolithium compounds or Grignards:

GaCl3 + 3MeMgBr → Me3Ga + 3MgBrCl

The electron-deficient nature of gallium can be removed by complex formation, for example

Me2GaCl + NH3 → [Me2Ga(NH3)Cl]+Cl−

Pi complex formation with alkynes is also known.

Organogallium compounds are reagents or intermediates in several classes of organic reactions:

Higher group 13 organometallic chemistry

The chemistry of organoindium (In) and organothallium (Tl) compounds parallel that of organogallium in many regards. Indium and thallium in oxidation state +1 are more common, for example the metallocenes cyclopentadienylindium(I) and cyclopentadienylthallium. Trimethylindium is important in the semiconductor industry. A special thallium feature is electrophilic thallation of arene compounds, reminiscent of mercuration (the group 12 neighbor). A common reagent for this purpose is thallium(III) trifluoroacetate. The intermediate arylthallium bisfluoroacetate can be isolated and converted to an aryl halide, aryl cyanide, aryl thiol or nitroarene. An example is the iodation of para-xylene.[5]

:

A specific niche indium research topic is indium mediated allylation.

See also

CH He
CLi CBe CB CC CN CO CF Ne
CNa CMg CAl CSi CP CS CCl CAr
CK CCa CSc CTi CV CCr CMn CFe CCo CNi CCu CZn CGa CGe CAs CSe CBr CKr
CRb CSr CY CZr CNb CMo CTc CRu CRh CPd CAg CCd CIn CSn CSb CTe CI CXe
CCs CBa CHf CTa CW CRe COs CIr CPt CAu CHg CTl CPb CBi CPo CAt Rn
Fr CRa Rf Db CSg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
↓
CLa CCe CPr CNd CPm CSm CEu CGd CTb CDy CHo CEr CTm CYb CLu
Ac CTh CPa CU CNp CPu CAm CCm CBk CCf CEs Fm Md No Lr
Chemical bonds to carbon
Core organic chemistry Many uses in chemistry
Academic research, but no widespread use Bond unknown

References

  1. ↑ C. Elschenbroich, A. Salzer Organometallics : A Concise Introduction (2nd Ed) (1992) from Wiley-VCH: Weinheim. ISBN 3-527-28165-7
  2. ↑ Chemistry of aluminium, gallium, indium, and thallium Anthony John Downs (Ed.) ISBN 978-0-7514-0103-5, 1993
  3. ↑ W, Uhl and M. R. Halvagar; et al. (2009). "Reducing Ga-H and Ga-C Bonds in Close Proximity to Oxidizing Peroxo Groups: Conflicting Properties in Single Molecules". Chemistry: A European Journal. 15 (42): 11298–11306. doi:10.1002/chem.200900746.
  4. ↑ GaCl3 in Organic Synthesis Ryo Amemiya and Masahiko Yamaguchi Eur. J. Org. Chem. 2005, 5145–5150 doi:10.1002/ejoc.200500512
  5. ↑ Organic Syntheses, Coll. Vol. 6, p.709 (1988); Vol. 55, p.70 (1976). Link
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