Di Bari Lorenzo, Pescitelli Gennaro, Sherry A Dean, Woods Mark
Dipartimento di Chimica e Chimica Industriale, Università di Pisa, via Risorgimento 35, 56126 Pisa, Italy.
Inorg Chem. 2005 Nov 14;44(23):8391-8. doi: 10.1021/ic0511118.
Studies of the structural, physical, and chemical properties of the lanthanide(III) complexes of DOTA (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)NO2BnDOTMA and S(SSSS)NO2BnDOTMA 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.
对DOTA(1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸)及相关配体的镧系元素(III)配合物的结构、物理和化学性质进行研究时,溶液中存在的两种配位异构体常常使研究变得复杂。由于这些配位异构体相互交换且无法分离,许多技术提供的信息仅关于这两种异构体的加权平均值。与配体S(RRRR)NO2BnDOTMA和S(SSSS)NO2BnDOTMA形成的镧系离子配合物在溶液中优先仅采用两种常见配位异构体中的一种,因此这些配体的镱配合物为单独研究每种配位几何结构的近红外圆二色性(NIR-CD)特征提供了独特的机会。获得的光谱支持了先前研究的许多结论和假设,并表明这种光谱对配位多面体的畸变特别敏感。在研究与(手性)主体和受体形成不稳定加合物的非手性YbDOTA类体系时,这将产生特别相关的结果。