tris-(Benzyltriazolylmethyl)amine

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Tris-(Benzyltriazolylmethyl)amine
Identifiers
PubChem 11203363
ChemSpider 9378431 YesY
Jmol-3D images Image 1
Properties
Molecular formula C30H30N10
Molar mass 530.63 g mol−1
 YesY (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

tris-(Benzyltriazolylmethyl)amine (TBTA) is a tertiary amine containing the 1,2,3-triazole moiety. When used as a ligand, complexed to copper(I), it allows for quantitative, regioselective formal Huisgen 1,3-dipolar cycloadditions between alkynes and azides, in a variety of aqueous and organic solvents.

It is believed that the ligand promotes catalysis through the stabilization of the copper(I)-oxidation state, while still allowing for the catalytic cycle of the CuAAC reaction to proceed.

X-ray analysis of the Cu(I) complex of tris(benzyltriazolylmethyl)amine revealed an unusual dinuclear dication with one triazole unit bridging two metal centers, and is an effective catalyst for the 'click' cycloaddition reaction. The X-ray structure of the complex of TBTA with Cu(II) is trigonal bipyramidal and can be reduced to the active 'click' catalyst form by sodium ascorbate, copper metal, or other reducing agents.

In the literature, it has been gaining widespread use as a biochemical tool for the tagging of proteins and enzymes. The compound is now commercially available through Sigma-Aldrich and Invitrogen. It may be prepared by the click reaction between tripropargylamine and benzyl azide:[1] [2]

Preparation of TBTA.png

[edit] References

  1. ^ Timothy R. Chan, Robert Hilgraf, K. Barry Sharpless, and Valery V. Fokin (2004). "Polytriazoles as Copper(I)-Stabilizing Ligands in Catalysis". Org. Lett. 6 (17): 2853–2855. doi:10.1021/ol0493094. PMID 15330631. 
  2. ^ Donnelly, P.S., Zanatta, S.D., Zammit, S.C., White, J.M., Williams, S.J. (2008). "‘“Click” Cycloaddition Catalysts: Copper(I) and Copper(II) tris-(Triazolylmethyl)amine Complexes’". Chem. Commun. (21): 2459–2461. doi:10.1039/b719724a. 
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