Department of Chemistry, Duke University, Durham, NC, 27708, USA.
Angew Chem Int Ed Engl. 2016 Oct 10;55(42):13086-13089. doi: 10.1002/anie.201606893.
Topological molecular connections and structures, including physical entanglements in polymer networks, knots along polymer chains, and rotaxanes in sliding ring gels, have important consequences for the physical properties of polymeric materials. Often these topologies contribute through their ability to bear mechanical stress, but experimental measures of their relative mechanical strength are rare. Here, we use sonochemical polymer mechanochemistry to assess the relative mechanical strength of a multicatenane copolymer relative to copolymers of cyclic and linear analogs. The relative mechanical strengths are obtained by comparing the limiting molecular weights (M ) and contour lengths (L ) of the polymers under pulsed ultrasound of their dilute solutions. The values of M and L , and thus the inferred mechanical strengths of the polymers, are effectively identical. The mechanical bonds of the catenanes are therefore as strong, or stronger, mechanically as the covalent bonds along the polymer backbone.
拓扑分子连接和结构,包括聚合物网络中的物理缠结、聚合物链上的纽结以及滑环凝胶中的轮烷,对聚合材料的物理性质有重要影响。这些拓扑结构通常通过承受机械应力的能力发挥作用,但它们的相对机械强度的实验测量却很少见。在这里,我们使用超声化学聚合物机械化学来评估多轮烷共聚物相对于环状和线性类似物共聚物的相对机械强度。通过比较其稀溶液在脉冲超声下的聚合物的极限分子量 (M) 和轮廓长度 (L) 来获得相对机械强度。聚合物的 M 和 L 值,以及由此推断出的机械强度,实际上是相同的。因此,轮烷的机械键与聚合物主链上的共价键一样坚固,或者更坚固。