Covalently immobilized tris(triazolyl) methanol-Cu(I) complexes: highly active and recyclable catalysts for CuAAC reactions

Date

2012-01-01

Author

ÖZKAL, Erhan
Özçubukçu, Salih
JİMENO, Ciril
Pericas, Miquel A.

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Tris(1-benzyl-1H-1,2,3-triazol-4-yl)methanol (3), a highly efficient ligand for CuAAC reactions, has been immobilized onto Merrifield resins through different strategies. The S(N)2-supported Cu complex (8) is stable in water and under air; it is active at low catalyst loadings (1 mol%) and at low concentration (down to 0.125 M) in both aqueous and purely organic media. Resin 8 can be repeatedly reused in 1 : 1 MeOH-water for short reaction times (4 h) with the only precaution of Cu(I) reloading every five cycles.

Subject Keywords

Azide-alkyne cycloaddition, Click chemistry, 1,3-dipolar cycloadditions, Huisgen cycloaddition, Ligands, Polymer, Organocatalyst, Ligation

URI

https://hdl.handle.net/11511/37953

Journal

CATALYSIS SCIENCE & TECHNOLOGY

DOI

https://doi.org/10.1039/c1cy00297j

Collections

Department of Chemistry, Article

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Citation Formats

E. ÖZKAL, S. Özçubukçu, C. JİMENO, and M. A. Pericas, “Covalently immobilized tris(triazolyl) methanol-Cu(I) complexes: highly active and recyclable catalysts for CuAAC reactions,” CATALYSIS SCIENCE & TECHNOLOGY, pp. 195–200, 2012, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/37953.