首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >Multinuclear and multifrequency NMR study of gadolinium(III) complexes with bis-amide derivatives of ethylenedioxydiethylene-dinitrilotetraacetic acid
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Multinuclear and multifrequency NMR study of gadolinium(III) complexes with bis-amide derivatives of ethylenedioxydiethylene-dinitrilotetraacetic acid

机译:III(III)与乙二氧基二乙烯-二三氟四乙酸双酰胺衍生物的配合物的多核和多频NMR研究

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New cationic gadolinium complexes have been synthesized and their ~1H and ~(17)O relaxometric properties investigated in view of their possible use as MRI contrast agents. The reaction of the bicyclic anhydride of ethylenedioxydiiethyl-enedinitrilotetraaacetic acid (H_4egta) with NH_3, isobutylamine and phenylpropylamine gave the octadentate bis-amide ligands 1-3 in high yields. The gadolinium(III) complexes were prepared from GdCl_3 and the acid form of the ligands. The stability constants of the complexes were obtained from potentiometric data and are about five orders of magnitude lower than for the parent [Gd(egta)]]~- complex. The magnetic field dependence of the proton relaxivity at 6.25 and 39 deg C was quantitatively analysed in order to obtain the relaxation parameters and indicated that one water molecule occupies a site of the co-ordination sphere of the complexes. The temperature dependence of the relaxivity, measured at 20 MHz, suggested that the water exchange rate, k_(ex) = 1/#tau#_M, is sensibly reduced compared to that of the parent compound. ~(17)O NMR data were acquired at 2.1 T and allowed an accurate estimation of #tau#_M which, at 298 K, resulted to be 230, 133 and 211 ns for Gd (centre dot) 1, Gd (centre dot) 2 and Gd (centre dot) 3 respectively. the two complexes bearing hydrophobic residues on the amide nitrogens form non-covalent adducts with serum albumin whose relaxivity is limited by the water exchange rate.
机译:已经合成了新的阳离子g络合物,并考虑到它们可能用作MRI造影剂,对它们的〜1H和〜(17)O弛豫特性进行了研究。乙二氧基二乙基-烯丙基三氯四乙酸(H_4egta)的双环酸酐与NH_3,异丁胺和苯丙胺的反应以高收率得到了八齿双酰胺配体1-3。 G(III)配合物是由GdCl_3和配体的酸形式制备的。配合物的稳定性常数是从电位数据中获得的,比母体[Gd(egta)]]-配合物低约五个数量级。为了获得弛豫参数,对6.25和39℃下质子弛豫的磁场依赖性进行了定量分析,结果表明一个水分子占据了配合物的配位球。在20 MHz下测得的弛豫率的温度依赖性表明,与母体化合物相比,水交换率k_(ex)= 1 /#tau#_M明显降低。在(2.1T)处获得〜(17)O NMR数据,并可以准确估计#tau#_M,在298 K时,Gd(中心点)1,Gd(中心点)分别为230、133和211 ns。 2和Gd(中心点)3。这两个在酰胺氮上带有疏水残基的配合物与血清白蛋白形成非共价加合物,其松弛度受水交换速率的限制。

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