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调节基于羟基吡啶酮的钆配合物的配位数:对磁共振成像造影剂的影响。

Tuning the coordination number of hydroxypyridonate-based gadolinium complexes: implications for MRI contrast agents.

作者信息

Pierre Valérie C, Botta Mauro, Aime Silvio, Raymond Kenneth N

机构信息

Department of Chemistry, University of California, Berkeley, California 94720-1460, USA.

出版信息

J Am Chem Soc. 2006 Apr 26;128(16):5344-5. doi: 10.1021/ja057805x.

DOI:10.1021/ja057805x
PMID:16620097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3188315/
Abstract

Eight-coordinate hydroxypyridinone/terephthalamide GdIII complexes display high relaxivities due to their two inner sphere water molecules. This relaxivity can be further increased by functionalizing the terephthalamide moiety with an amine. A significant hydrogen bonding interaction between the amine and another water molecule close to the GdIII apparently facilitates its coordination on the open site of the metal. The resulting nine-coordinate complex has three inner sphere water molecules, while maintaining high stability and fast ligand exchange rates.

摘要

八配位的羟基吡啶酮/对苯二甲酰胺钆(III)配合物由于其两个内界水分子而具有高弛豫率。通过用胺对苯二甲酰胺部分进行功能化,可以进一步提高这种弛豫率。胺与靠近钆(III)的另一个水分子之间存在显著的氢键相互作用,这显然促进了其在金属开放位点上的配位。所得的九配位配合物有三个内界水分子,同时保持高稳定性和快速的配体交换速率。

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