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New bis(triazinyl) pyridines for selective extraction of americium(iii)
183
Citations
31
References
2006
Year
New HydrophobicInorganic ChemistryChemical EngineeringCrystal StructureEngineeringHeterocyclicNew BisOrganic ChemistryBioorganometallic ChemistryChemistryHeterocycle ChemistrySynthetic ChemistryInorganic SynthesisReference Molecule
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 In order to increase the stability of 1 and 2, the labile α-benzylic hydrogens that are present in 7 have been replaced by alkyl groups.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.
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