首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Cooperative Counterion-Polyion Interactions in Polyelectrolyte Chain Dynamics: NMR and Quantum-Chemical Study of Locally Collapsed State in Dilute Poly(N-diallyldimethylammonium chloride) in NaCl/D_2O Solutions
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Cooperative Counterion-Polyion Interactions in Polyelectrolyte Chain Dynamics: NMR and Quantum-Chemical Study of Locally Collapsed State in Dilute Poly(N-diallyldimethylammonium chloride) in NaCl/D_2O Solutions

机译:聚电解质链动力学中的协同抗衡离子-离子相互作用:NaCl / D_2O溶液中稀聚(N-二烯丙基二甲基氯化铵)的局部塌陷状态的NMR和量子化学研究

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Using ~1H and ~(35)Cl single- and double-quantum NMR spectra, relaxation and pulsed gradient spin echo (PGSE) diffusion experiments combined with quantum-chemical calculations, we studied the molecular dynamics of poly(N-diallyldimethylammonium chloride) (PDADMAC) and its copolymers with acrylamide in D_2O under conditions of various ionic strength determined by the concentration of the polyelectrolyte itself or an added salt or both. According to absolute signal intensity, only 12-15% of the DADMAC groups are in an actual mobile stage, giving rise to detectable signals. Transverse relaxation analysis shows a wide mobility distribution in the mobile groups. Double quantum ~1H NMR signals of N-methyl proton evidence motional anisotropy relative to the NMR time window and thus motional hindering in part of the visible DADMAC groups. Strong dependence of these phenomena on ionic strength, as well as quantum-chemical simulations, indicates that these phenomena are of an electrostatic nature. Probing of the counterion distribution and dynamics by ~(35)Cl NMR quadrupolar relaxation shows that a majority of counterions behave according to the Halle-Wennerstrom-Picullel model based on combined Poisson-Boltzmann and Smoluchowski equations, but relaxation of the T_2~3 coherence indicates that a smaller part of the counterions correlate with the polymer motion. Accordingly, the mobile part of the polymer is interpreted as a fluctuation consisting of a locally collapsed chain and condensed counterions. By three independent methods, namely, inversion-recovery, transverse relaxation, and in particular, saturation transfer experiments, the average lifetime of this fluctuation was estimated to be in the range 30-80 ms. Thus, the fluctuation is frozen, that is, it is stabilized by cooperative interaction between the collapsed part of the chain and the condensed counterions. Mutual exchange between group with different mobility, found by saturation transfer experiment, indicates that the fluctuation can move to-and-fro along the chain.
机译:使用〜1H和〜(35)Cl单和双量子NMR光谱,弛豫和脉冲梯度自旋回波(PGSE)扩散实验与量子化学计算相结合,我们研究了聚(N-二烯丙基二甲基氯化铵)的分子动力学( (PDADMAC)及其在D_2O中与丙烯酰胺的共聚物,其离子强度由聚电解质本身或添加的盐或两者的浓度决定,具有各种不同的离子强度。根据绝对信号强度,只有12-15%的DADMAC组处于实际的移动级,从而产生可检测的信号。横向弛豫分析显示了移动组中广泛的移动性分布。 N-甲基质子的双量子〜1H NMR信号证明相对于NMR时间窗的运动各向异性,因此在部分可见DADMAC基团中存在运动障碍。这些现象对离子强度的强烈依赖性以及量子化学模拟表明,这些现象具有静电性质。通过〜(35)Cl NMR四极弛豫探测抗衡离子分布和动力学,结果表明,大多数抗衡离子根据基于Poisson-Boltzmann和Smoluchowski方程组合的Halle-Wennerstrom-Picullel模型,但具有T_2〜3相干弛豫表示抗衡离子的较小部分与聚合物运动相关。因此,聚合物的可移动部分被解释为由局部塌陷的链和缩合的平衡离子组成的波动。通过三种独立的方法,即反演恢复,横向弛豫,尤其是饱和传递实验,该波动的平均寿命估计在30-80 ms的范围内。因此,波动被冻结,也就是说,通过链的塌陷部分与缩合的抗衡离子之间的协同相互作用来稳定波动。通过饱和转移实验发现,具有不同迁移率的群体之间的相互交换表明,波动可以沿着链条来回移动。

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