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Complexation of Cm(<scp>iii</scp>) and Eu(<scp>iii</scp>) with CyMe<sub>4</sub>-BTPhen and CyMe<sub>4</sub>-BTBP studied by time resolved laser fluorescence spectroscopy

Antje BremerKarlsruher Institut für Technologie, Institut für Nukleare Entsorgung, P.O. Box 3640, 76021 Karlsruhe, Germany. [email protected]Daniel M. WhittakerCentre of Radiochemistry Research, School of Chemistry, The University of Manchester, Oxford Road, Manchester M13 9PL, UKClint A. SharradCentre of Radiochemistry Research, School of Chemistry, The University of Manchester, Oxford Road, Manchester M13 9PL, UKAndreas GeistKarlsruher Institut für Technologie, Institut für Nukleare Entsorgung, P.O. Box 3640, 76021 Karlsruhe, GermanyPetra J. PanakKarlsruher Institut für Technologie, Institut für Nukleare Entsorgung, P.O. Box 3640, 76021 Karlsruhe, Germany
2013en
ABI

Аннотация

The complexation of Cm(III) and Eu(III) with 2,9-bis(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-1,2,4-benzotriazin-3-yl)-1,10-phenanthroline (CyMe4-BTPhen) and 6,6'-bis(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-1,2,4-benzotriazin-3-yl)-2,2'-bipyridine (CyMe4-BTBP) in methanolic solution was investigated by TRLFS. For both ligands, the 1:2 complex with the particular metal ion is the only species observed in equilibrated samples. The species distribution for various ligand concentrations was determined and stability constants of the 1:2 complexes were derived (log β2 = 13.8 ± 0.2 (Cm(III)-CyMe4-BTPhen), log β2 = 11.6 ± 0.4 (Eu(III)-CyMe4-BTPhen), log β2 = 12.4 ± 0.3 (Cm(III)-CyMe4-BTBP) and log β2 = 11.3 ± 0.3 (Eu(III)-CyMe4-BTBP)). Biphasic experiments in combination with TRLFS studies on the organic phase revealed the formation of ternary complexes with two CyMe4-BTPhen or -BTBP molecules and additional coordination of a nitrate anion as species formed during the extraction process.

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