Jakobi Bruno, Bichler Karin J, Juranyi Fanni, Schneider Gerald J
Department of Chemistry, Louisiana State University, Baton Rouge, Louisiana 70803, USA.
Laboratory for Neutron Scattering, Paul Scherrer Institute, CH-5232 Villigen, Switzerland.
J Chem Phys. 2024 Feb 28;160(8). doi: 10.1063/5.0184429.
The segmental dynamics of bottlebrush polymers with a stiff backbone and flexible side chains has been studied. The segmental relaxation time of side chains attached to a flexible backbone follows the same trend as linear polymers, an increase with the increasing molecular weight, but is slowed down compared to their linear counterparts. Theoretical work predicts a reversal of the molecular weight dependence of the relaxation time for stiff backbones. As a model for a stiff-g-flexible system, bottlebrushes with poly(norbornene) backbone and poly(propylene oxide) side chains, PNB-g-PPO, at a uniform grafting density have been synthesized and characterized with quasi-elastic neutron scattering. Indeed, the anticipated reversed dynamics was found. Increasing the side chain length decreases the segmental relaxation time. This indicates the importance of the characteristics of the grafting site beyond a simplified picture of an attached side chain. The mean square displacement shows a similar trend with longer side chains exhibiting a larger displacement.
对具有刚性主链和柔性侧链的刷状聚合物的链段动力学进行了研究。连接在柔性主链上的侧链的链段弛豫时间与线性聚合物遵循相同的趋势,即随着分子量的增加而增加,但与线性对应物相比有所减慢。理论研究预测,刚性主链的弛豫时间对分子量的依赖性会发生反转。作为刚性 - g - 柔性体系的模型,已合成了具有聚(降冰片烯)主链和聚(环氧丙烷)侧链、接枝密度均匀的刷状聚合物PNB - g - PPO,并通过准弹性中子散射对其进行了表征。确实,发现了预期的反转动力学。增加侧链长度会缩短链段弛豫时间。这表明接枝位点特性的重要性,超出了连接侧链的简化图景。均方位移呈现出类似的趋势,较长的侧链表现出更大的位移。