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首页> 外文期刊>Inorganica Chimica Acta >INTERMOLECULAR INTERACTIONS OF HIGHLY STABLE PARAMAGNETIC LANTHANIDE(III) CHELATES AS STUDIED BY NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY
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INTERMOLECULAR INTERACTIONS OF HIGHLY STABLE PARAMAGNETIC LANTHANIDE(III) CHELATES AS STUDIED BY NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY

机译:核磁共振波谱研究的高度稳定的顺磁性镧系元素(Ⅲ)螯合物的分子间相互作用

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The paramagnetic C-13 NMR relaxation rate enhancements and the H-1 induced chemical shifts of a series of organic molecules, caused by various paramagnetic metal complexes and a nitroxide radical (TEMPOL), were measured in aqueous solution. These NMR perturbations were used to study and model the mechanisms of their non-covalent intel actions. The paramagnetic metal complexes showed a varying degree of binding specificity, in contrast to the non-specific interactions of the nitroxide radical. Weak and basically non-specific binding was observed for the neutral DTPA-bis(amide) complexes, possibly due to hydrophobic interactions, whereas the single negatively charged DOTA and DOTP-MB complexes showed weak specific interactions with ammonium functions. The strongest and most specific interactions occurred between the negatively charged Ln(DOTP) chelates and the protonated linear and macrocyclic amines. In the case of Ln(DOTP)-ADA, the H-1 induced shifts and C-13 spin-lattice relaxation rates were fitted to the theoretical equations, yielding a geometry for the adduct where the ammonium group interacts with the Ln-unbound negatively charged oxygen(s) of one phosphonate group. Two Ln( DOTP) molecules appear to be able to sandwich the diprotonated tetraazamacrocyclic amine CY. In the polyhydroxyammonium compound MEG, the strong electrostatic interaction is assisted by hydrogen bonding of hydroxyl groups to the Ln-unbound phosphonate oxygens of DOTP. A comparison of the strong pH dependences found for the paramagnetic NMR effects of the Ln(DOTP) chelates on the H-1 and C-13 nuclei of CY and MEG clearly indicated the dominance of the electrostatic interactions in both cases. Considering the organic molecules used as good models of side-chains of amino-acid residues at the surface of proteins, the observed interactions allow specific probing of protein surfaces using NMR methods. [References: 55]
机译:在水溶液中测量了由各种顺磁性金属络合物和一氧化氮自由基(TEMPOL)引起的顺磁性C-13 NMR弛豫速率增强和一系列有机分子的H-1诱导化学位移。这些NMR扰动用于研究和模拟其非共价智力作用的机理。与氮氧化物自由基的非特异性相互作用相反,顺磁性金属配合物显示出不同程度的结合特异性。中性DTPA-双(酰胺)配合物观察到弱和基本上非特异性结合,可能是由于疏水相互作用,而单个带负电荷的DOTA和DOTP-MB配合物显示出弱的与铵功能的特异性相互作用。带负电荷的Ln(DOTP)螯合物与质子化的线性和大环胺之间发生了最强和最特定的相互作用。在Ln(DOTP)-ADA的情况下,将H-1诱导的位移和C-13自旋晶格弛豫速率与理论方程式拟合,得出加合物的几何形状,其中铵基团与Ln-未结合的负离子相互作用一个膦酸酯基团的带电氧。两个Ln(DOTP)分子似乎能够将双质子化的四氮杂大环胺CY夹在中间。在多羟基铵化合物MEG中,强大的静电相互作用是通过羟基与DOTP的Ln-未结合的膦酸酯氧的氢键键合来辅助的。对Ln(DOTP)螯合物对CY和MEG的H-1和C-13核的顺磁性NMR效应发现的强pH依赖性的比较清楚地表明,在两种情况下,静电相互作用均占优势。考虑到将有机分子用作蛋白质表面氨基酸残基侧链的良好模型,观察到的相互作用使得可以使用NMR方法对蛋白质表面进行特异性探测。 [参考:55]

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