Abstract
The dynamic (radial and rotational) couplings between diatomic molecular states are considered for the case that these states are 'dressed' by a strong, external magnetic field. The explicit form of the dynamic coupling operator is derived within the classical-trajectory approximation to the internuclear motion. The radial and rotational coupling matrix elements are expressed in a form suitable for efficient numerical evaluation.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Journal of Physics B: Atomic, Molecular and Optical Physics
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
