Department of Chemistry, The Pennsylvania State University, University Park, PA 16802 (USA) http://www.psu.edu/dept/phillipsgroup/index.html.
Angew Chem Int Ed Engl. 2015 Oct 26;54(44):13063-7. doi: 10.1002/anie.201506511. Epub 2015 Sep 8.
Adhesives that selectively debond from a surface by stimuli-induced head-to-tail continuous depolymerization of poly(benzyl ether) macro-cross-linkers within a poly(norbornene) matrix are described. Continuous head-to-tail depolymerization provides faster rates of response than can be achieved using a small-molecule cross-linker, as well as responses to lower stimulus concentrations. Shear-stress values for glass held together by the adhesive reach 0.51±0.10 MPa, whereas signal-induced depolymerization via quinone methide intermediates reduces the shear stress values to 0.05±0.02 MPa. Changing the length of the macro-cross-linkers alters the time required for debonding, and thus enables the programmed sequential release of specific layers in a glass composite material.
描述了一种通过刺激诱导的聚(苯醚)大分子交联剂的头尾连续解聚,从表面选择性解键合的粘合剂。与使用小分子交联剂相比,连续的头尾解聚提供了更快的响应速率,并且可以对更低的刺激浓度做出响应。通过粘合剂连接在一起的玻璃的剪切应力值达到 0.51±0.10 MPa,而通过醌甲叉中间体引发的信号诱导解聚将剪切应力值降低至 0.05±0.02 MPa。改变大分子交联剂的长度会改变解键合所需的时间,从而能够在玻璃复合材料中按程序顺序释放特定的层。