Time-Resolved Molecular Frame Dynamics of Fixed-in-Space CS2 Molecules

被引:278
作者
Bisgaard, Christer Z. [1 ]
Clarkin, Owen J. [1 ,2 ]
Wu, Guorong [1 ]
Lee, Anthony M. D. [1 ,2 ]
Gessner, Oliver [3 ]
Hayden, Carl C. [4 ]
Stolow, Albert [1 ,2 ]
机构
[1] Natl Res Council Canada, Steacie Inst Mol Sci, Ottawa, ON K1A 0R6, Canada
[2] Queens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
[3] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Chem Sci, Berkeley, CA 94720 USA
[4] Sandia Natl Labs, Combust Res Facil, Livermore, CA 94551 USA
基金
加拿大自然科学与工程研究理事会;
关键词
PHOTOELECTRON ANGULAR-DISTRIBUTIONS; LASER-PULSES; SPECTROSCOPY; STATE; PREDISSOCIATION; DIFFRACTION; DISSOCIATION; IONIZATION; NM;
D O I
10.1126/science.1169183
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Random orientation of molecules within a sample leads to blurred observations of chemical reactions studied from the laboratory perspective. Methods developed for the dynamic imaging of molecular structures and processes struggle with this, as measurements are optimally made in the molecular frame. We used laser alignment to transiently fix carbon disulfide molecules in space long enough to elucidate, in the molecular reference frame, details of ultrafast electronic-vibrational dynamics during a photochemical reaction. These three-dimensional photoelectron imaging results, combined with ongoing efforts in molecular alignment and orientation, presage a wide range of insights obtainable from time-resolved studies in the molecular frame.
引用
收藏
页码:1464 / 1468
页数:5
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