首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Dynamic NMR properties of DOTA ligand: variable pH and temperature ~1H NMR study on [K(H_xDOTA)]~((3-x)-) species
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Dynamic NMR properties of DOTA ligand: variable pH and temperature ~1H NMR study on [K(H_xDOTA)]~((3-x)-) species

机译:DOTA配体的动态NMR特性:在[K(H_xDOTA)]〜((3-x)-)物种上变化的pH和温度〜1H NMR研究

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摘要

The ~1H NMR spectra of [H_xDOTA]~((4-x)-) species are reported as a function of pH and temperature in aqueous solution. The spectra show line broadening both in ligand proton signals and also in the water proton signal by titration with KOH solution. The formation of different [K(H_xDOTA)]~((3-x)-) complexes is found to be responsible for this behaviour. At high pH the usual fluxional motions, i.e. the ring inversion and the change in the acetate arms' helicity, which are also characteristic for other but inert metal-DOTA complexes, have been detected. However, because of the kinetic lability of K~+-O and K~+-N coordinative bonds a new type of rearrangement appears. This new motion requires breaking of coordinative bonds in the complex and can be described as a certain type of ring slewing around the ring C-C bonds. At low temperature (about 270 K) the ring slewing slows down and becomes negligible compared with the ring inversion and the change in the arms' helicity. These two latter processes have the same rate. When the temperature is higher (about 320 K) the ring slewing accelerates and its rate exceeds the rate of ring inversion. At this temperature the change in the acetate arms' helicity has the same rate as the ring slewing. Additionally, in the pH range 4-5 a slow intermolecular proton exchange process has been observed between the water and the dissociable protons of [K(H_xDOTA)]~((3-x)-). A water-assisted proton exchange mechanism is proposed on the basis of the activation parameters. This finding supports the previously suggested slow proton motion hypothesis for the formation of DOTA complexes.
机译:据报道,[H_xDOTA]〜((4-x)-)物种的〜1H NMR光谱是水溶液中pH和温度的函数。光谱显示通过用KOH溶液滴定,配体质子信号和水质子信号中的线变宽。发现不同的[K(H_xDOTA)]〜((3-x)-)配合物的形成是这种行为的原因。在高pH下,已检测到通常的通量运动,即环反转和乙酸酯臂螺旋度的变化,这对于其他但惰性的金属-DOTA配合物也是特征。然而,由于K〜+ -O和K〜+ -N配位键的动力学不稳定性,出现了一种新型的重排。这种新的运动需要破坏复合物中的配位键,并且可以被描述为围绕环C-C键的某种特定类型的环。在低温(约270 K)下,与环形反转和手臂螺旋度的变化相比,环形回转的速度变慢并且可以忽略不计。后两个过程的速率相同。当温度较高时(约320 K),环形回转加速,其速度超过环形反转的速度。在此温度下,醋酸酯臂的螺旋度变化与环回转的速率相同。另外,在pH范围4-5中,在水和[K(H_xDOTA)]〜((3-x)-)的可解离质子之间观察到缓慢的分子间质子交换过程。根据活化参数,提出了一种水辅助质子交换机理。该发现支持了先前提出的用于形成DOTA复合物的慢质子运动假说。

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