Control of a chemical reaction far from the Franck-Condon point by single-pulse resonant and non-resonant light-matter interaction.
(2007) In Journal of the American Chemical Society 129(43). p.13014-13021- Abstract
- Using optimal control as a spectroscopic tool we decipher the details of the molecular dynamics of the essential multidimensional excited-state photoisomerization - a fundamental chemical reaction of key importance in biology. Two distinct nuclear motions are identified in addition to the overall bond-twisting motion: Initially, the reaction is dominated by motion perpendicular to the torsion coordinate. At later times, a second optically active vibration drives the system along the reaction path to the bottom of the excited-state potential. The time scales of the wavepacket motion on a different part of the excited-state potential are detailed by pump-shaped dump optimal control. This technique offers new means to control a chemical... (More)
- Using optimal control as a spectroscopic tool we decipher the details of the molecular dynamics of the essential multidimensional excited-state photoisomerization - a fundamental chemical reaction of key importance in biology. Two distinct nuclear motions are identified in addition to the overall bond-twisting motion: Initially, the reaction is dominated by motion perpendicular to the torsion coordinate. At later times, a second optically active vibration drives the system along the reaction path to the bottom of the excited-state potential. The time scales of the wavepacket motion on a different part of the excited-state potential are detailed by pump-shaped dump optimal control. This technique offers new means to control a chemical reaction far from the Franck-Condon point of absorption and to map details of excited-state reaction pathways revealing unique insights into the underlying reaction mechanism. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/938899
- author
- Dietzek, Benjamin LU ; Brüggemann, Ben LU ; Pascher, Torbjörn LU and Yartsev, Arkady LU
- organization
- publishing date
- 2007
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- PROBE SPECTROSCOPY, POPULATION TRANSFER, PHOTO ISOMERIZATION, QUANTUM CONTROL, PHOTOISOMERIZATION, RETINAL ISOMERIZATION, GAS-PHASE, PULSE, CHEMICAL-REACTIONS, LASER CONTROL
- in
- Journal of the American Chemical Society
- volume
- 129
- issue
- 43
- pages
- 13014 - 13021
- publisher
- The American Chemical Society (ACS)
- external identifiers
-
- wos:000250818900035
- scopus:35848938505
- ISSN
- 1520-5126
- DOI
- 10.1021/ja072639+
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Chemical Physics (S) (011001060)
- id
- 31ae669c-d3d3-44d7-a37c-d9bd55ac6f30 (old id 938899)
- date added to LUP
- 2016-04-01 16:14:12
- date last changed
- 2022-03-14 23:08:20
@article{31ae669c-d3d3-44d7-a37c-d9bd55ac6f30, abstract = {{Using optimal control as a spectroscopic tool we decipher the details of the molecular dynamics of the essential multidimensional excited-state photoisomerization - a fundamental chemical reaction of key importance in biology. Two distinct nuclear motions are identified in addition to the overall bond-twisting motion: Initially, the reaction is dominated by motion perpendicular to the torsion coordinate. At later times, a second optically active vibration drives the system along the reaction path to the bottom of the excited-state potential. The time scales of the wavepacket motion on a different part of the excited-state potential are detailed by pump-shaped dump optimal control. This technique offers new means to control a chemical reaction far from the Franck-Condon point of absorption and to map details of excited-state reaction pathways revealing unique insights into the underlying reaction mechanism.}}, author = {{Dietzek, Benjamin and Brüggemann, Ben and Pascher, Torbjörn and Yartsev, Arkady}}, issn = {{1520-5126}}, keywords = {{PROBE SPECTROSCOPY; POPULATION TRANSFER; PHOTO ISOMERIZATION; QUANTUM CONTROL; PHOTOISOMERIZATION; RETINAL ISOMERIZATION; GAS-PHASE; PULSE; CHEMICAL-REACTIONS; LASER CONTROL}}, language = {{eng}}, number = {{43}}, pages = {{13014--13021}}, publisher = {{The American Chemical Society (ACS)}}, series = {{Journal of the American Chemical Society}}, title = {{Control of a chemical reaction far from the Franck-Condon point by single-pulse resonant and non-resonant light-matter interaction.}}, url = {{http://dx.doi.org/10.1021/ja072639+}}, doi = {{10.1021/ja072639+}}, volume = {{129}}, year = {{2007}}, }