Structural and chiroptical properties of the two coordination isomers of YbDOTA-type complexes

被引:39
作者
Di Bari, L
Pescitelli, G
Sherry, AD
Woods, M
机构
[1] Univ Pisa, Dipartimento Chim & Chim Ind, I-56126 Pisa, Italy
[2] Univ Texas, Dept Chem, Richardson, TX 75080 USA
[3] Univ Texas, SW Med Ctr, Rogers Magnet Resonance Ctr, Dallas, TX 75235 USA
[4] Macrocyclics, Dallas, TX 75235 USA
关键词
D O I
10.1021/ic0511118
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Studies of the structural, physical, and chemical properties of the lanthanide(III) complexes of DCTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid) and related ligands are often complicated by the presence of two coordination isomers in solution. Since these coordination isomers are in exchange and cannot be separated, many techniques offer information only on the weighted average of the two isomers. Lanthanide ion complexes formed with the ligands S(RRRR)NO(2)BnDOTMA and S(SSSS)NO(2)BnDOTMA preferentially adopt only one of the two common coordination isomers in solution, so the ytterbium complexes of these ligands offer a unique opportunity to study the near-infrared circular dichroism (NIR-CD) characteristics of each coordination geometry in isolation. The spectra acquired support many of the conclusions and assumptions of previous studies and demonstrate that this spectroscopy is particularly sensitive to the distortion of the coordination polyhedron. This will have particularly relevant consequences when studying achiral YbDOTA-like systems forming labile adducts with (chiral) hosts and receptors.
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页码:8391 / 8398
页数:8
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