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Identification of slow dynamic processes in poly(n-hexyl methacrylate) by solid-state 1D-MAS exchange NMR

机译:固态1D-MAS交换NMR鉴定聚甲基丙烯酸正己酯中的慢动力学过程

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摘要

The molecular dynamics of the different molecular subunits in the amorphous polymer poly-(n-hexyl methacrylate), PnHMA, was investigated by recently developed solid-state 1D-MAS exchange NMR methods at temperatures close to the glass transition temperature. The molecular mobility of main-chain, side-chain, and carboxyl carbons could be assigned to different relaxation processes as identified by dielectric and mechanical relaxation spectroscopy as well as caloric methods. Information about both the time constants as well as the geometry of the processes could be obtained. It was found that the side chain contributes in the dynamic window of NMR exchange experiments (tau(c) approximate to 1 ms to 0.1 s) mainly to the beta process while the main chain and carboxyl group are found to contribute to both the beta and alpha processes. The data suggest that the contributions of side and main chain to the beta process are qualitatively different. All dynamic processes exhibit a wide distribution of correlation times. The proper separation of spin-exchange processes from the molecular dynamics is demonstrated. [References: 55]
机译:通过最近开发的固态1D-MAS交换NMR方法,在接近玻璃化转变温度的温度下研究了非晶态聚合物聚(甲基丙烯酸正己酯)PnHMA中不同分子亚基的分子动力学。主链碳原子,侧链碳原子和羧基碳原子的分子迁移率可以分配给不同的弛豫过程,这可以通过介电和机械弛豫谱以及热量方法来确定。可以获得有关时间常数以及过程的几何形状的信息。发现侧链在NMR交换实验的动态窗口中起作用(tau(c)大约为1 ms至0.1 s),主要影响β过程,而发现主链和羧基对β和β均起作用。 alpha进程。数据表明,侧链和主链对β过程的贡献在质量上是不同的。所有动态过程都显示出相关时间的广泛分布。证明了自旋交换过程与分子动力学的正确分离。 [参考:55]

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