期刊
DALTON TRANSACTIONS
卷 43, 期 6, 页码 2684-2694出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3dt52204k
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资金
- German Federal Ministry of Education and Research (BMBF) [02NUK020A, 02NUK020D]
- foundation of the Energie Baden-Wurttemberg (EnBW)
- Commission of the European Community (project ACTINET-I3)
- MBASE consortium
- EPSRC [EP/G037140/1]
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-tetrahydro1,2,4- 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 beta(2) = 13.8 +/- 0.2 (Cm(III)-CyMe4-BTPhen), log beta(2) = 11.6 +/- 0.4 (Eu(III)-CyMe4-BTPhen), log beta(2) = 12.4 +/- 0.3 (Cm(III)-CyMe4-BTBP) and log beta(2) = 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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