Chemistry:Organoindium chemistry

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Short description: Chemistry of compounds with a carbon to indium bond

Organoindium chemistry is the chemistry of compounds containing In-C bonds. The main application of organoindium chemistry is in the preparation of semiconducting components for microelectronic applications. The area is also of some interest in organic synthesis. Most organoindium compounds feature the In(III) oxidation state, akin to its lighter congeners Ga(III) and B(III).[1]

thumb|166px|right|Trimethylindium

Organoindium(I)

Monovalent In is relatively more common than Ga(I) or B(I). One example is cyclopentadienylindium(I).

Structure of CpIn, which is a polymer (red = In)[2]
Structure of [InC(tms)3]4, an In(I) tetrahedrane (dark gray = In)[3]

Organoindium(III)

Trimethylindium is a colorless, volatile solid. It is the preferred source of indium for metalorganic vapour phase epitaxy (MOVPE) of indium-containing compound semiconductors, such as InP, InAs, AlInGaNP, etc. InMe3 is pyrophoric.

To obtain the trialkyl derivatives, alkylation of indium trihalides with organolithium reagents is typical.[4]

OrganoIn(III) compounds are also prepared by treating In metal with alkyl halides. This reaction gives mixed organoindium halides. Illustrative is the reaction of allyl bromide with a THF suspension of indium. Both monoallylindium dibromide and diallylindium bromide are produced.[5]

Two intermediates formed during IMA.svg

A variety of organoindium(III) species such as InRX3− and solvates of RXIn+, R2In+, and X2In+ are thought to rapidly interconvert at room temperature.[6]

Indium-mediated allylations (IMA)

IMAs proceed in two steps: first, indium reacts with the allyl halide, give an allyl-In(III) intermediate, second, this allyl indide reacts with an electrophile:
Two steps of the IMA reaction mechanism
The reaction is conducted under the conditions of a Barbier reaction where the indium, allyl halide, and electrophile are all mixed in a one-pot process. Indium alkylates more readily than other metals, such as Mg, Pb, Bi, or Zn and does not require a promoter or organic solvent. IMAs have advantages over other carbon bond forming reactions because of their ability to be carried out in water (see Green chemistry).[7] [8] Although indium mediated allylations can be carried out in aqueous media, a variety of other solvents may be used including THF (tetrahydrofuran), DMF (dimethylformamide), room temperature ionic liquids, NMF (n-methylformamide), and others. [9] [10] Solvent often affects the solubility, rate of the reaction, yield, stability, regioselectivity, and stereoselectivity. Indium mediates the allylation of a wide variety of electrophiles. The examples in the following scheme illustrate the breadth of applications of IMA.

A wide variety of IMA reactions.svg

Selectivity

Organoindium intermediates do not react with –OH or –CO2H groups. Reactions with carbonyls, however, give high yields. Research has shown that in reactions of an indium intermediate with an electrophilic compound of both aldehyde and ketone, the reaction proceeded with the aldehyde. The electrophilic compound is shown below.[11]

Updated chemoselective propargylation of aldehyde.svg

The regioselectivity of allylation mediated by indium in water is dependent on the steric effects of the substituents on both the intermediate and carbonyl. An α-attack from the nucleophile (at the position bearing the halogen) is distinguishable from a γ-attack (at the double bond) by inspecting the products. The scheme below gives an example of two different products formed from the same nucleophile under α-regioselectivity (α) and γ-regioselectivity (γ). This regioselectivity does not appear to depend on conjugation or the degree of substitution. [12]

Example of ima showing alpha vs gamma.svg

The addition of allylindium reagents to aldehydes substituted at α or β carbons can be very diastereoselective in aqueous systems. For example, if chelation control is present in an α-oxy aldehyde, the product is expected to be the syn diastereomer. A sample reaction of chelation versus non-chelation control is illustrated below.

Ima example showing diastereoselectivity.svg

Numerous investigations have found an explanation for this effect. The oxygens of the carbonyl and the hydroxyl group chelate the indium of the organoindium intermediate as illustrated below on the left by the two green bonds. The incipient C-C bond, illustrated in red, creates a six-member ring in a chair conformation. Under chelation control, the allyl group attacks the carbonyl carbon from the less hindered side opposite to that of the R group. Once the C-C bond is fully formed, the indium is released, producing the syn diol. A similar chelated structure is relevant to the allylation of β-oxy aldehydes results in anti diols.[13][14]

Explanation of diastereoselectivity of IMA.svg

The addition of allylindium reagents to electrophilic hydrazones, illustrated below, has been reported to synthesize only one enantiomer of the chiral product with up to 97% selectivity using binol as a chiral additive.[15] Similarly, a chiral amino alcohol allows for extremely high enantioselectivity in the allylation of ketones.[16] The indium-mediated allylation in water is especially useful in carbohydrate synthesis (such as sialic acids), without using protecting groups. [17]

Corrected example of enantioselective IMA.svg

Another example of enantioselective IMA.svg

See also

References

  1. ↑ Shen, Zhi-Liang; Wang, Shun-Yi; Chok, Yew-Keong; Xu, Yun-He; Loh, Teck-Peng (2013). "Organoindium Reagents: The Preparation and Application in Organic Synthesis". Chemical Reviews 113: 271–401. doi:10.1021/cr300051y. PMID 23110495. 
  2. ↑ Beachley O. T.; Pazik J. C.; Glassman T. E.; Churchill M. R.; Fettinger J.C.; Blom R. (1988). "Synthesis, characterization and structural studies of In(C5H4Me) by x-ray diffraction and electron diffraction techniques and a reinvestigation of the crystalline state of In(C5H5) by x-ray diffraction studies". Organometallics 7: 1051–1059. doi:10.1021/om00095a007. 
  3. ↑ Uhl, Werner; Graupner, Rene; Layh, Marcus; Schütz, Uwe (1995). "In4{C(SiMe3)3}4 mit In4-tetraeder und In4Se4{C(SiMe3)3}4 mit In4Se4-heterocubanstruktur". Journal of Organometallic Chemistry 493: C1–C5. doi:10.1016/0022-328X(95)05399-A. 
  4. ↑ Kopasz, J. P.; Hallock, R. B.; Beachley, O. T. (1986). "Tris[(Trimethylsilyl)Methyl]Indium". Inorganic Syntheses 24: 89–91. doi:10.1002/9780470132555.ch27. 
  5. ↑ Yasuda, M; Haga, M; Nagaoka, Y; Baba, A. Eur. J. Org. Chem. 2010, 5359–5363.
  6. ↑ Koszinowski, K. J. Am. Chem. Soc. 2010, 132, 6032–6040.
  7. ↑ Li, C.-J.; Chan, T.-H. Organic Reactions in Aqueous Media with Indium, Tetrahedron Lett. 1991, 32, 7017-7020 doi:10.1016/0040-4039(91)85028-4.
  8. ↑ Li, C.-J.; Chan, T. H. Organic Syntheses Using Indium-Mediated and Catalyzed Reactions In Aqueous Media, Tetrahedron 1999, 55, 11149-11176 doi:10.1016/S0040-4020(99)00641-9.
  9. ↑ Frimpong, K; Wzorek, J; Lawlor, C; Spencer, K; Mitzel. T; J. Org. Chem. 2009, 74, 5861–5870. doi:10.1021/jo900763u
  10. ↑ Law, M.C; Cheung, T.W; Wong, K.Y; Chan, T.H. J. Org. Chem. 2007, 72, 923–929.
  11. ↑ Haddad, T.D; Hirayama, L.C; Buckley, J.J; Singaram, B. J. Org. Chem. 2012, 77, 889–898.
  12. ↑ Isaac, M.B; Chan, T.H. Tetrahedron Lett. 1995, 36, 8957–8960.
  13. ↑ Paquette, L.A; Mitzel, T.M. J. Am. Chem. Soc. 1996, 118, 1931–1937.
  14. ↑ "Allylindation in Aqueous Media: Methyl 3-(Hydroxymethyl)-4-Methyl-2-Methylenepentanoate". Organic Syntheses 77: 107. 2000. doi:10.15227/orgsyn.077.0107. 
  15. ↑ Cook, G.R; Kargbo, R; Maity, B. Org. Lett. 2005, 7, 2767–2770.
  16. ↑ Haddad, T.D; Hirayama, L.C; Taynton, P; Singaram, B. Tetrahedron Lett. 2008, 49, 508–511.
  17. ↑ Chan, T.-H.; Li, C.-J. A Concise Chemical Synthesis of (+) 3-Deoxy-D-glycero-D-galacto-nonulsonic acid (KDN) J. Chem. Soc., Chem. Commun. 1992, 747-748.doi:10.1039/C39920000747



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