Zsabka, Peter’s team published research in Solvent Extraction and Ion Exchange in 2020 | CAS: 510758-28-8

Tris((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)amine(cas: 510758-28-8) can stabilizes Cu(I) towards disproportionation and oxidation thus enhancing its catalytic effect in the azide-acetylene cycloaddition.Recommanded Product: 510758-28-8

《Solvent Extraction Studies for the Separation of Trivalent Actinides from Lanthanides with a Triazole-functionalized 1,10-phenanthroline Extractant》 was written by Zsabka, Peter; Opsomer, Tomas; Van Hecke, Karen; Dehaen, Wim; Wilden, Andreas; Modolo, Giuseppe; Verwerft, Marc; Binnemans, Koen; Cardinaels, Thomas. Recommanded Product: 510758-28-8 And the article was included in Solvent Extraction and Ion Exchange in 2020. The article conveys some information:

A new N-atom donor extractant 2,9-bis(1-(2-ethylhexyl)-1H-1,2,3-triazol-4-yl)-1,10-phenanthroline (EH-BTzPhen) was synthesized and used in solvent extraction studies to sep. the trivalent minor actinide americium(III) and curium(III) from europium(III), representing fission product lanthanides. The extractant was found to be soluble in 1-octanol and in the Aliquat-336 nitrate ([A336][NO3]) ionic liquid diluent, but insoluble in n-dodecane. The [A336][NO3] is a fully incinerable room temperature ionic liquid, and has a higher flash point than aliphatic diluents such as 1-octanol. The EH-BTzPhen proved to be effective for selective minor actinide extraction only in combination with 2-bromohexanoic acid synergist when 1-octanol was used as a diluent (SFAm/Eu > 200). The change of the diluent from 1-octanol to Aliquat-336 nitrate allowed selective An(III) extraction from low acidity feed solutions without the need of a synergist (SFAm/Eu ∼ 70 and SFAm/Cm ∼ 1.9-2.2). The phase transfer kinetics of the ligand-metal complexes is however very slow at 22°C in the case of both solvents. With this newly synthesized extractant, the achieved SFAm/Cm was comparable to the values achieved with the established CyMe4BTBP and CyMe4BTPhen extractants. After reading the article, we found that the author used Tris((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)amine(cas: 510758-28-8Recommanded Product: 510758-28-8)

Tris((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)amine(cas: 510758-28-8) can stabilizes Cu(I) towards disproportionation and oxidation thus enhancing its catalytic effect in the azide-acetylene cycloaddition.Recommanded Product: 510758-28-8

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics