Aime S, Botta M, Terreno E, Anelli P L, Uggeri F
Departimento di Chimica Inorganica, Chimica Fisica E Chimica dei Materiali, Università di Torino, Italy.
Magn Reson Med. 1993 Nov;30(5):583-91. doi: 10.1002/mrm.1910300509.
The relaxation properties of Gd(DOTP)5- (1, 4, 7, 10-tetra-azacyclododecane- N,N',N'',N'''-tetrakis(methylenephosphonic acid)) have been investigated as a function of pH, temperature, concentration, and magnetic field strength. We have found that the complex has one exchangeable water molecule in its inner coordination sphere, at a distance of 3.26 A from the metal ion, and it does not form oligomers in solution in the concentration range 0.2 to 10 mM. The possible presence of two species in solution with an average fractional hydration number is also taken into accounts. The NMRD profiles were recorded at 5 degrees C, 25 degrees C, and 35 degrees C and quantitatively analyzed in terms of the paramagnetic relaxation equations. Interestingly the addition to a solution of the Gd(III)-complex of nitrogen bases results in a marked relaxation enhancement, which shows a strong pH dependence with a maximum around pH = 9. The relaxivity gain has been shown to depend on outer-sphere effects originating from multiple electrostatic interactions between the anionic complex and the organic cations that bring the exchangeable protons of the substrate molecules in to close proximity with the paramagnetic center. High resolution NMR relaxation data for N-methyl-D(-)-glucamine suggest that the hydroxyl group on the beta-carbon plays a role in stabilizing the interaction, presumably through a hydrogen bond with an uncoordinated oxygen atom of the complex.
已研究了钆(DOTP)5-(1,4,7,10-四氮杂环十二烷-N,N',N'',N'''-四(亚甲基膦酸))的弛豫特性与pH值、温度、浓度和磁场强度的关系。我们发现该配合物在其内部配位球中有一个可交换水分子,距离金属离子3.26埃,并且在0.2至10 mM的浓度范围内在溶液中不形成低聚物。还考虑了溶液中可能存在的两种具有平均分数水合数的物种。在5℃、25℃和35℃下记录了NMRD谱,并根据顺磁弛豫方程进行了定量分析。有趣的是,向钆(III)配合物溶液中添加氮碱会导致弛豫显著增强,这显示出强烈的pH依赖性,在pH = 9左右达到最大值。已表明弛豫率增益取决于外层效应,该效应源于阴离子配合物与有机阳离子之间的多重静电相互作用,这些相互作用使底物分子的可交换质子与顺磁中心紧密接近。N-甲基-D(-)-葡甲胺的高分辨率NMR弛豫数据表明,β-碳上的羟基可能通过与配合物的未配位氧原子形成氢键,在稳定相互作用中发挥作用。