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Updated: Jun 23, 2026

Direct Imaging of Laser-driven Ultrafast Molecular Rotation
Published on: February 4, 2017
Rotationally inelastic collisions of CN(A(2)Pi) with small molecules
Ani Khachatrian1, Paul J Dagdigian
1Department of Chemistry, The Johns Hopkins University, Baltimore, Maryland 21218-2685, USA.
Abstract:
An optical-optical double resonance technique has been utilized to investigate rotational energy transfer of selected rotational/fine-structure levels of CN(A(2)Pi, v = 3) in collisions with the molecular partners CO(2) and CH(4). Total removal rate constants for several rotational/fine-structure levels were measured for both collision partners. State-to-state relative rate constants were determined for several initial levels. These show a strikingly strong collisional propensity to conserve the fine-structure/Lambda-doublet label, akin to our previous observations with the N(2) collision partner. The possible origin of this propensity is discussed.
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