揭示排除体积对树状大分子取向弛豫动力学的影响

IF 2.9 3区 化学 Q3 CHEMISTRY, PHYSICAL
Shelly Bhardwaj, Amit Kumar
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引用次数: 0

摘要

本研究利用优化的劳斯-齐姆形式,研究了柔性枝状大分子的取向弛豫动力学,同时纳入了非键单体之间排除的体积相互作用。排除体积效应通过δ函数伪势建模为相邻非键单体之间的有效共体积,而流体动力相互作用则使用预平均Oseen张量。这项工作检查\( P_2^{(i)}(t) \)作为树状大分子生成的功能和最近的非键单体之间的排除体积相互作用的强度。理论框架建立在库马尔和比斯瓦斯(物理学家)的工作基础上。化学。化学。物理。[j], 2013, 15, 20294],该研究分析了半柔性枝状大分子的取向弛豫,但没有考虑排除的体积相互作用。在不同的排除体积参数\( v_\theta \)和\( v_\psi \)下,\( P_2^{(i)}(t) \)的时间衰减趋势与不同温度下的实验观测一致。\cite{yimer2012static}通过\( P_2^{(i)}(t) \)的傅立叶余弦变换得到的谱密度\( J(\omega) \)受排除的体积相互作用的显著影响。在高频状态下,\( J(\omega) \)随着频率的增加而减小,在中频范围内表现出一种交叉模式,因为排除的体积相互作用不同。谱密度曲线下的面积随着排除体积参数\( v_\theta \)和\( v_\psi \)的减小而增大。降低的自旋-晶格弛豫率\( [1/T_{1H}] \)在中频范围内遵循幂律缩放,其指数依赖于树状大分子的生成和排除的体积相互作用的强度。值得注意的是,对于生成\( G = 5 \),在\( v_\theta = 0.24 \)和\( v_\psi = 2.12 \)计算的缩放指数与实验数据精确对齐,\cite{yimer2012static}验证了理论模型。自旋-自旋弛豫率\( \left[ \frac{1}{T_{2H}} \right] \)受排除的体积相互作用的影响有明显的趋势。在中频区域,其标度行为与结构约束和节段运动密切相关,由于低频贡献的增强,在较低的相关时间偏离\( \left[ \frac{1}{T_{1H}} \right] \)。然而,对于\( G=5 \)代,\( \left[ \frac{1}{T_{2H}} \right] \)遵循与\( \left[ \frac{1}{T_{1H}} \right] \)相似的趋势,并且与实验观察结果很好地吻合。 \cite{yimer2012static}
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unraveling the Influence of Excluded Volume on Orientational Relaxation Dynamics in Dendrimers
This study investigates the orientational relaxation dynamics of flexible dendrimers while incorporating excluded volume interactions among non-bonded monomers using the optimized Rouse-Zimm formalism. Excluded volume effects are modeled as an effective co-volume between adjacent non-bonded monomers through a delta function pseudopotential, while hydrodynamic interactions are accounted for using the preaveraged Oseen tensor. This work examines \( P_2^{(i)}(t) \) as a function of dendrimer generation and the strength of excluded volume interactions between nearest non-bonded monomers. The theoretical framework builds upon the work of [Kumar and Biswas (Phys. Chem. Chem. Phys., 2013, 15, 20294)], which analyzed orientational relaxation in semiflexible dendrimers but did not consider excluded volume interactions. The temporal decay of \( P_2^{(i)}(t) \) at varying excluded volume parameters, \( v_\theta \) and \( v_\psi \), shows trends consistent with experimental observations under different temperatures.~\cite{yimer2012static} The spectral density, \( J(\omega) \), obtained via the Fourier cosine transform of \( P_2^{(i)}(t) \), is significantly influenced by excluded volume interactions. In the high-frequency regime, \( J(\omega) \) decreases with increasing frequency, exhibiting a crossover pattern as excluded volume interactions vary in the intermediate frequency range. The area under the spectral density curve increases as the excluded volume parameters \( v_\theta \) and \( v_\psi \) decrease. The reduced spin-lattice relaxation rate, \( [1/T_{1H}] \), follows a power-law scaling in the intermediate frequency regime, with exponents dependent on dendrimer generation and the strength of excluded volume interactions. Notably, for generation \( G = 5 \), the calculated scaling exponent at \( v_\theta = 0.24 \) and \( v_\psi = 2.12 \) aligns precisely with experimental data,~\cite{yimer2012static} validating the theoretical model. The spin-spin relaxation rate, \( \left[ \frac{1}{T_{2H}} \right] \), exhibits a distinct trend influenced by excluded volume interactions. In the intermediate frequency regime, its scaling behavior is closely linked to structural constraints and segmental motion, deviating from \( \left[ \frac{1}{T_{1H}} \right] \) at lower correlation times due to enhanced low-frequency contributions. However, for generation \( G=5 \), \( \left[ \frac{1}{T_{2H}} \right] \) follows a similar trend to \( \left[ \frac{1}{T_{1H}} \right] \) and aligns well with experimental observations.~\cite{yimer2012static}
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来源期刊
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
5.50
自引率
9.10%
发文量
2675
审稿时长
2.0 months
期刊介绍: Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
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