Comparison of structural dynamics and coherence of d-d and MLCT light-induced spin state trapping

被引:47
|
作者
Zerdane, S. [1 ]
Wilbraham, L. [2 ]
Cammarata, M. [1 ]
Iasco, O. [3 ]
Riviere, E. [3 ]
Boillot, M-L. [3 ]
Ciofini, I. [2 ]
Collet, E. [1 ]
机构
[1] Univ Rennes 1, Inst Phys Rennes, UMR 6251, UBL, F-35042 Rennes, France
[2] PSL Res Univ, Inst Rech Chim Paris, CNRS, Chim ParisTech, 11 Rue Pierre & Marie Curie, F-75005 Paris, France
[3] Univ Paris Saclay, Univ Paris Sud, CNRS, Inst Chim Mol & Mat Orsay,UMR 8182, Orsay, France
基金
欧洲研究理事会;
关键词
RAY-ABSORPTION SPECTROSCOPY; ROOM-TEMPERATURE; LASER-PULSE; CROSSOVER COMPLEXES; RELAXATION; CRYSTAL; PHOTOMAGNETISM; BISTABILITY; COMPOUND; SYSTEMS;
D O I
10.1039/c6sc05624e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Light-induced excited spin state trapping (LIESST) in Fe-II spin-crossover systems is a process that involves the switching of molecules from low (LS, S = 0) to high spin (HS, S = 2) states. The direct LS-to-HS conversion is forbidden by selection rules, and LIESST involves intermediate states such as (MLCT)-M-1,3 or T-1,T-3. The intersystem crossing sequence results in an HS state, structurally trapped by metal-ligand bond elongation through the coherent activation and damping of molecular breathing. The ultrafast dynamics of this process has been investigated in FeN6 ligand field systems, under MLCT excitation. Herein, we studied LIESST in an (FeN4O2)-N-II spin-crossover material of lower symmetry, which allowed for quite intense and low-energy shifted d-d bands. By combining ab initio DFT and TD-DFT calculations and fs optical absorption measurements, we demonstrated that shorter intermediates enhanced coherent structural dynamics, and d-d excitation induced faster LS-to-HS switching, compared to MLCT.
引用
收藏
页码:4978 / 4986
页数:9
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