Dipole-Resonance Assisted Isomerization in the Electronic Ground State Using Few-Cycle Infrared Pulses
Author:
Affiliation:
1. Institut für Theoretische Chemie, Universität Wien, Währinger Strasse 17, A-1090 Wien, Austria
2. Institut für Physik, Montanuniversität Leoben, Franz-Josef Strasse 18, 8700 Leoben, Austria
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jp112419z
Reference42 articles.
1. Intense few-cycle laser fields: Frontiers of nonlinear optics
2. X-ray Pulses Approaching the Attosecond Frontier
3. Generation of attosecond unidirectional half-cycle pulses: Inclusion of propagation effects
4. Carrier-envelope phase-sensitive inversion in two-level systems
5. Theory of ultrafast laser control of isomerization reactions in an environment: Picosecond cope rearrangement of substituted semibullvalenes
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1. On the quantum and classical control of laser-driven isomerization in the Wigner representation;The Journal of Chemical Physics;2021-05-07
2. Quantum control of isomerization by robust navigation in the energy spectrum;The Journal of Chemical Physics;2015-12-07
3. Coherent chemistry with THz pulses: Ultrafast field-driven isomerization of LiNC;Physical Review A;2015-05-18
4. Laser-Driven Isomerization of HCN → HNC: The Importance of Rotational Excitation;The Journal of Physical Chemistry A;2015-03-17
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