Structural Dynamics upon Photoexcitation in a Spin Crossover Crystal Probed with Femtosecond Electron Diffraction

被引:78
作者
Jiang, Yifeng [1 ]
Liu, Lai Chung [2 ,3 ]
Mueller-Werkmeister, Henrike M. [1 ]
Lu, Cheng [2 ,3 ]
Zhang, Dongfang [1 ]
Field, Ryan L. [2 ,3 ]
Sarracini, Antoine [2 ,3 ]
Moriena, Gustavo [2 ,3 ]
Collet, Eric [4 ]
Miller, R. J. Dwayne [1 ]
机构
[1] Max Planck Inst Struct & Dynam Matter, Luruper Chaussee 149, D-22607 Hamburg, Germany
[2] Univ Toronto, Dept Chem, 80 St George St, Toronto, ON M5S 3H6, Canada
[3] Univ Toronto, Dept Phys, 80 St George St, Toronto, ON M5S 3H6, Canada
[4] Univ Rennes 1, CNRS, Inst Phys Rennes, UMR 6251,UBL, F-35042 Rennes, France
基金
加拿大自然科学与工程研究理事会;
关键词
electron diffraction; N ligands; photochemistry; spin crossover; structure elucidation; HARD X-RAY; ABSORPTION-SPECTROSCOPY; IRON(II); PHASE; STATE; CRYSTALLOGRAPHY; TRANSITIONS; RELAXATION; CHARGE;
D O I
10.1002/anie.201702497
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photoexcitation of spin crossover (SCO) complexes can trigger extensive electronic spin transitions and transformation of molecular structure. However, the precise nature of the associated ultrafast structural dynamics remains elusive, especially in the solid state. Here, we studied a single-crystal SCO material with femtosecond electron diffraction (FED). The unique capability of FED allows us to directly probe atomic motions and to track ultrafast structural changes within a crystal lattice. By monitoring the time-dependent changes of the Bragg reflections, we observed the formation of a photoinduced structure similar to the thermally induced high-spin state. The data and refinement calculations indicate the global structural reorganization within 2.3 ps, as the metal-ligand bond distribution narrows during intramolecular vibrational energy redistribution (IVR) driving the intermolecular rearrangement. Three independent dynamical group are identified to model the structural dynamics upon photoinduced SCO.
引用
收藏
页码:7130 / 7134
页数:5
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