Environmental effects on mechanochemical activation of spiropyran in linear PMMA

被引:120
作者
Beiermann, Brett A. [1 ,2 ]
Davis, Douglas A. [1 ,3 ]
Kramer, Sharlotte L. B. [1 ,2 ]
Moore, Jeffrey S. [1 ,3 ]
Sottos, Nancy R. [1 ,2 ]
White, Scott R. [1 ,4 ]
机构
[1] Beckman Inst Adv Sci & Technol, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Mat Sci & Engn, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[4] Univ Illinois, Dept Aerosp Engn, Urbana, IL 61801 USA
关键词
TRANSFER RADICAL POLYMERIZATION; MECHANICAL FORCE; POLY(METHYL METHACRYLATE); POLYMERS; CATALYSTS; PATHWAYS; STRESS;
D O I
10.1039/c0jm03967e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Mechanophore-linked linear poly(methyl methacrylate) (PMMA) was synthesized using bisfunctionalized spiropyran (SP) as an atom transfer radical polymerization initiator. The resulting polymer had a T(g) of 127 degrees C and molecular weight greater than 250 kDa. SP-cleavage experiments confirmed the incorporation of SP molecules approximately into the center of the polymer chain. Force-induced reaction of the SP species into a colored, fluorescent merocyanine (MC) form was investigated over a range of environmental conditions by monitoring color change or full field fluorescence during tensile loading. Activation of this glassy polymer was observed in a temperature range of 90-105 degrees C. At higher temperatures, approaching T(g), deformation was dominated by viscous flow at very low applied stress with no activation. At lower temperatures, brittle failure preceded activation unless the polymer was plasticized by exposure to methanol. Mechanically induced activation of SP in plasticized PMMA at room temperature (22 degrees C) was achieved at a critical strain (ca. 10%) substantially below that required in previous systems.
引用
收藏
页码:8443 / 8447
页数:5
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