Department of Chemistry, Katholieke Universiteit Leuven, Leuven, Belgium.
Chemphyschem. 2001 Dec 17;2(12):767-9. doi: 10.1002/1439-7641(20011217)2:12<767::AID-CPHC767>3.0.CO;2-E.
Chiroptical properties and absolute configuration have been correlated for a series of Ln(oda)3 complexes in aqueous solution (Ln=Pr, Nd, Sm, Eu, Tb, Dy, Ho, Er, or Tm; oda=2,2'-oxydiacetic acid). Addition of the chiral probe L-proline (L-Pro) to a series of the racemic complexes resulted in an excess of the Λ-enantiomer.
手性光学性质和绝对构型已经被关联到一系列Ln(oda)3配合物在水溶液中(Ln=Pr, Nd, Sm, Eu, Tb, Dy, Ho, Er, 或 Tm;oda=2,2'-氧二乙酸)。向一系列外消旋配合物中加入手性探针 L-脯氨酸(L-Pro),导致过量的 Λ-对映体。