Institut de Physique de Rennes, UMR 6251 UR1-CNRS, Bat 11A Campus de Beaulieu, University Rennes 1, Rennes, France.
Phys Chem Chem Phys. 2012 May 14;14(18):6192-9. doi: 10.1039/c2cp23587k. Epub 2012 Jan 31.
We report the spin state photo-switching dynamics in two polymorphs of a spin-crossover molecular complex triggered by a femtosecond laser flash, as determined by combining femtosecond optical pump-probe spectroscopy and picosecond X-ray diffraction techniques. The light-driven transformations in the two polymorphs are compared. Combining both techniques and tracking how the X-ray data correlate with optical signals allow understanding of how electronic and structural degrees of freedom couple and play their role when the switchable molecules interact in the active crystalline medium. The study sheds light on crossing the border between femtochemistry at the molecular scale and femtoswitching at the material scale.
我们通过结合飞秒光泵浦探测光谱学和皮秒 X 射线衍射技术,报告了在飞秒激光脉冲触发下,两种螺旋-交叉分子配合物的多晶型体中自旋态光开关动力学的超快过程。我们比较了两种多晶型体的光驱动转变。结合这两种技术,并跟踪 X 射线数据与光学信号的相关性,有助于理解在可切换分子在活性晶态介质中相互作用时,电子和结构自由度如何耦合并发挥作用。该研究揭示了分子尺度上的飞秒化学和材料尺度上的飞秒开关之间的交叉。