Conditional repair by locally switching the thermal healing capability of dynamic covalent polymers with light

被引:86
作者
Fuhrmann, Anne [1 ,2 ]
Goestl, Robert [1 ,2 ]
Wendt, Robert [1 ,2 ]
Koetteritzsch, Julia [3 ,4 ]
Hager, Martin D. [3 ,4 ]
Schubert, Ulrich S. [3 ,4 ]
Brademann-Jock, Kerstin [5 ]
Thuenemann, Andreas F. [5 ]
Noechel, Ulrich [6 ,7 ]
Behl, Marc [6 ,7 ]
Hecht, Stefan [1 ,2 ]
机构
[1] Humboldt Univ, Dept Chem, Brook Taylor Str 2, D-12489 Berlin, Germany
[2] Humboldt Univ, IRIS Adlershof, Brook Taylor Str 2, D-12489 Berlin, Germany
[3] Friedrich Schiller Univ, Lab Organ & Macromol Chem IOMC, Humboldtstr 10, D-07743 Jena, Germany
[4] Friedrich Schiller Univ, Jena Ctr Soft Matter, Philosophenweg 7, D-07743 Jena, Germany
[5] Fed Inst Mat Res & Testing, Unter Eichen 87, D-12205 Berlin, Germany
[6] Helmholtz Zentrum Geesthacht, Inst Biomat Sci, Kantstr 55, D-14513 Teltow, Germany
[7] Helmholtz Zentrum Geesthacht, Berlin Brandenburg Ctr Regenerat Therapies BCRT, Dept Act Polymers, Kantstr 55, D-14513 Teltow, Germany
来源
NATURE COMMUNICATIONS | 2016年 / 7卷
基金
欧洲研究理事会;
关键词
SUPRAMOLECULAR POLYMERS; MOLECULAR SWITCH; CHEMISTRY; COPOLYMER; HYDROGELS;
D O I
10.1038/ncomms13623
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Healable materials could play an important role in reducing the environmental footprint of our modern technological society through extending the life cycles of consumer products and constructions. However, as most healing processes are carried out by heat alone, the ability to heal damage generally kills the parent material's thermal and mechanical properties. Here we present a dynamic covalent polymer network whose thermal healing ability can be switched 'on' and 'off' on demand by light, thereby providing local control over repair while retaining the advantageous macroscopic properties of static polymer networks. We employ a photoswitchable furan-based crosslinker, which reacts with short and mobile maleimide-substituted poly(lauryl methacrylate) chains forming strong covalent bonds while simultaneously allowing the reversible, spatiotemporally resolved control over thermally induced de-and re-crosslinking. We reason that our system can be adapted to more complex materials and has the potential to impact applications in responsive coatings, photolithography and microfabrication.
引用
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页数:7
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