Femtosecond multidimensional imaging of a molecular dissociation

被引:158
作者
Gessner, O
Lee, AMD
Shaffer, JP
Reisler, H
Levchenko, SV
Krylov, AI
Underwood, JG
Shi, H
East, ALL
Wardlaw, DM
Chrysostom, ET
Hayden, CC
Stolow, A
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 Oklahoma, Dept Phys & Astron, Norman, OK 73019 USA
[4] Univ So Calif, Dept Chem, Los Angeles, CA 90089 USA
[5] Open Univ, Dept Phys & Astron, Milton Keynes MK7 6AA, Bucks, England
[6] Univ Regina, Dept Chem, Regina, SK S4S 0A2, Canada
[7] Sandia Natl Labs, Combust Res Facil, Livermore, CA 94551 USA
关键词
D O I
10.1126/science.1120779
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
The coupled electronic and vibrational motions governing chemical processes are best viewed from the molecule's point of view-the molecular frame. Measurements made in the laboratory frame often conceal information because of the random orientations the molecule can take. We used a combination of time-resolved photoelectron spectroscopy, multidimensional coincidence imaging spectroscopy, and ab initio computation to trace a complete reactant-to-product pathway-the photodissociation of the nitric oxide dimer-from the molecule's point of view, on the femtosecond time scale. This method revealed an elusive photochemical process involving intermediate electronic configurations.
引用
收藏
页码:219 / 222
页数:4
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