Sandia National Laboratories, Livermore, California 94551, USA.
ACS Appl Mater Interfaces. 2010 Jun;2(6):1594-600. doi: 10.1021/am100050v.
A photochromic polymer exhibiting mechanochromic behavior is prepared by means of ring-opening polymerization (ROP) of epsilon-caprolactone by utilizing a difunctional indolinospiropyran as an initiator. The configuration of having the photochromic initiating species within the polymer backbone leads to a mechanochromic effect with deformation of polymer films leading to ring-opening of the spiro C-O bond to form the colored merocyanine. Active stress monitoring by dynamic mechanical analysis (DMA) in tension mode was used to probe the effects of UV irradiation on polymer films held under constant strain. Irradiation with UV light induces a negative change in the polymer stress of approximately 50 kPa. Finally, a model of the mechanochromic effect was performed using density functional theory (DFT) and time-dependent DFT (TDDFT) calculations. A sharp increase in the relative molecular energy and the absorption wavelength as well as a drastic decrease in the spiro-oxygen atom charge occurred at a molecular elongation of >39%.
通过利用双官能吲哚螺吡喃作为引发剂对ε-己内酯进行开环聚合(ROP),制备了一种表现出机械变色行为的光致变色聚合物。具有光致变色引发物种在聚合物主链内的结构导致机械变色效应,聚合物薄膜的变形导致螺 C-O 键的开环,形成有色的硫靛。通过拉伸模式的动态力学分析(DMA)进行主动应力监测,以探测在恒定应变下保持的聚合物薄膜中 UV 照射的影响。UV 光照射导致聚合物应力约降低 50 kPa。最后,使用密度泛函理论(DFT)和含时密度泛函理论(TDDFT)计算对机械变色效应进行了建模。在分子伸长>39%时,相对分子能量和吸收波长急剧增加,而螺氧原子电荷急剧下降。