Nanosecond-Lived Excimer Observation in a Crystal of a Rhodium(I) Complex via Time-Resolved X-ray Laue Diffraction

被引:1
作者
Laski, Piotr [1 ]
Bosman, Lerato [2 ]
Drapala, Jakub [1 ,3 ]
Kaminski, Radoslaw [1 ]
Szarejko, Dariusz [1 ]
Borowski, Patryk [1 ]
Roodt, Andreas [2 ]
Henning, Robert [4 ]
Brink, Alice [2 ]
Jarzembska, Katarzyna N. [1 ]
机构
[1] Univ Warsaw, Dept Chem, PL-02089 Warsaw, Poland
[2] Univ Free State, Dept Chem, ZA-9301 Bloemfontein, South Africa
[3] Warsaw Univ Technol, Fac Chem, PL-00664 Warsaw, Poland
[4] Univ Chicago, Ctr Adv Radiat Sources, Chicago, IL 60637 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2024年
基金
芬兰科学院; 美国国家卫生研究院; 瑞士国家科学基金会; 新加坡国家研究基金会;
关键词
METALLOPHILIC INTERACTIONS; STRUCTURAL DYNAMICS; LIGHT; CRYSTALLOGRAPHY; PHOTOCHEMISTRY; CARBONYLATION; PATHWAYS; TOOLKIT; PROTEIN; CU(I);
D O I
10.1021/acs.jpclett.4c02476
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
The rare observation of transient Rh<middle dot><middle dot><middle dot>Rh excimer formation in a single crystal is reported. The estimated excited-state lifetime at 100 K is 2 ns, which makes it the shortest-lived small-molecule species caught experimentally using the laser-pump/X-ray-probe time-resolved Laue method. Upon excitation with 390 nm laser light, the intermolecular Rh<middle dot><middle dot><middle dot>Rh distance decreases from 3.379(4) to 3.19(1) & Aring;, and the metal-metal contact gains more bonding character. On the basis of the experimental results and theoretical modeling, the structural changes determined with 100 ps time resolution reflect principally the S-0 -> S-1 electronic transition.
引用
收藏
页码:10301 / 10306
页数:6
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