McNair Olivia D, Brent Davis P, Sparks Bradley J, Patton Derek L, Savin Daniel A
School of Polymers and High Performance Materials, University of Southern Mississippi , 118 College Drive #5050, Hattiesburg, Mississippi 39406, United States.
ACS Appl Mater Interfaces. 2014 May 14;6(9):6088-97. doi: 10.1021/am405138e. Epub 2014 Feb 26.
We report the physical properties of thiol-ene networks modified with thiourethane or urethane linkages, either along the main chain or as a branched component in the network, respectively. Because of the robust and orthogonal nature of thiol-isocyanate and thiol-ene reactions, these networks can be formed in a two-step, one-pot synthesis. Resultant networks were characterized using dynamic mechanical analysis, mechanical testing and other complementary techniques. It was found that incorporating (thio)urethanes into the networks increased Tg, but also increased strain at break and toughness while decreasing cross-link density. The changes in physical properties are discussed in terms of a proposed dual network morphology. These facile modifications to thiol-ene networks demonstrate how molecular-level, nanoscale changes can have a profound influence on the macroscale properties through hierarchical development of network morphology.
我们分别报道了用硫代聚氨酯或聚氨酯键修饰的硫醇-烯网络的物理性质,这些修饰分别沿着主链或作为网络中的支链成分。由于硫醇-异氰酸酯和硫醇-烯反应具有稳健性和正交性,这些网络可以通过两步一锅法合成。使用动态力学分析、力学测试和其他补充技术对所得网络进行了表征。结果发现,将(硫代)聚氨酯引入网络中会提高玻璃化转变温度(Tg),但同时也会增加断裂应变和韧性,同时降低交联密度。根据所提出的双网络形态对物理性质的变化进行了讨论。对硫醇-烯网络的这些简便修饰表明,分子水平、纳米尺度的变化如何通过网络形态的分级发展对宏观性质产生深远影响。