Force-induced activation of covalent bonds in mechanoresponsive polymeric materials

被引:0
作者
Douglas A. Davis
Andrew Hamilton
Jinglei Yang
Lee D. Cremar
Dara Van Gough
Stephanie L. Potisek
Mitchell T. Ong
Paul V. Braun
Todd J. Martínez
Scott R. White
Jeffrey S. Moore
Nancy R. Sottos
机构
[1] Department of Chemistry,Department of Aerospace Engineering
[2] ,undefined
[3] Department of Mechanical Science and Engineering,undefined
[4] ,undefined
[5] The Beckman Institute,undefined
[6] ,undefined
[7] Department of Materials Science and Engineering,undefined
[8] ,undefined
[9] University of Illinois at Urbana-Champaign,undefined
[10] Illinois 61801,undefined
[11] USA,undefined
[12] Present addresses: School of Mechanical and Aerospace Engineering,undefined
[13] Nanyang Technological University,undefined
[14] Singapore (J.Y.); Department of Chemistry,undefined
[15] Stanford University,undefined
[16] Stanford,undefined
[17] California,undefined
[18] USA (T.J.M.).,undefined
来源
Nature | 2009年 / 459卷
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摘要
Biology is replete with materials systems that actively and functionally respond to mechanical stimuli and thereby enable physiological processes such as the sense of touch, hearing or the growth of tissue and bone. In contrast, exposing polymers to large stresses tends to result in covalent bond rupture and hence damage or failure. Davis et al. now demonstrate that synthetic materials can be rationally designed to ensure that mechanical stress alters their properties in a useful manner. This is realized by incorporating a chemical group that responds to mechanical stress by changing its colour to red as it undergoes a ring-opening reaction, enabling the team to directly monitor the accumulation of plastic deformation. The principles underpinning this work should enable the development of other force-responsive chemical groups that could impart synthetic materials with desirable functionalities ranging from damage sensing to fully regenerative self-healing.
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页码:68 / 72
页数:4
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