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New bis(triazinyl) pyridines for selective extraction of americium(iii)

New Journal of Chemistry · 2006 · Vol. 30(8) · pp. 1171–1171
Michael J. HudsonCarole BoucherDamien BraekersJean F. DesreuxMichael G. B. DrewM.R.St.J. ForemanLaurence M. HarwoodCl ment HillC. MadicFrank MarkenTristan G. A. Youngs

Abstract

New hydrophobic, tridentate nitrogen heterocyclic reagents (BATPs) such as 2,6-bis(5,5,8,8-tetramethyl-5,6,7,8-tetrahydrobenzo[1,2,4]triazin-3-yl) pyridine (1) and 2,6-bis(9,9,10,10-tetramethyl-9,10-dihydro-1,2,4-triaza-anthrane-3-yl) pyridine (2) have been studied. 1 is resistant to hydrolysis in 3 M nitric acid, whereas 2 is resistant to both acid hydrolysis and radiolysis. The molecules are able to give significantly enhanced separations of americium(III) from an excess of europium(III) in nitric acid. Typically, for 1DAm = 500 and SFAm/Eu = 5000 compared with DAm = 30 and SFAm/Eu = 400 with the reference molecule 2,6-bis(isopropyl[1,2,4]triazin-3-yl) pyridine (7). In order to increase the stability of 1 and 2, the labile α-benzylic hydrogens that are present in 7 have been replaced by alkyl groups. Three molecules of 1 are able to enclose completely the coordination sphere of the M(III) in the crystal structure of [Y(1)3][Y(NO3)5]·NO3·2.5H2O.

Radioactive element chemistry and processingLanthanide and Transition Metal ComplexesChemical Synthesis and CharacterizationChemistryAmericiumPyridineNitric acidEuropiumMoleculeMedicinal chemistryAlkylHydrolysisReagent

Funding

  • European Commission
  • University of Reading
  • Engineering and Physical Sciences Research Council
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