Related Experiment Video
Updated: Jul 11, 2025

Temperature-Controlled Assembly and Characterization of a Droplet Interface Bilayer
Published on: April 19, 2021
Stereodynamical Control of D3+ Formation from the Bimolecular Photoreaction in the D2-D2 Dimer
Lianrong Zhou1, Junjie Qiang2, Hao Huang1
1State Key Laboratory of Precision Spectroscopy, East China Normal University, Shanghai 200241, China.
Abstract:
We report the stereodynamic control of D3+ formation from the laser-induced bimolecular reaction in a weakly bound D2-D2 dimer via impulsive molecular alignment. Using a linearly polarized moderately intense femtosecond pump pulse, the D2 molecules in the dimer were prealigned prior to the bimolecular reaction triggered by a delayed probe pulse. The rotationally excited D2 in the dimer was observed to rotate freely as if it were a monomer. It was demonstrated that the yield of photoreaction product D3+ is increased or decreased when the molecular axis of D2 is parallel or perpendicular to the probe laser polarization, respectively. The underlying physics of this steric effect is the alignment-dependent bond cleavage of D2+ in the dimer induced by a photon-coupled parallel transition.
More Related Videos
08:22Calibration-free In Vitro Quantification of Protein Homo-oligomerization Using Commercial Instrumentation and Free, Open Source Brightness Analysis Software
Published on: July 17, 2018
07:36Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
Related Concept Videos
Diels–Alder Reaction Forming Cyclic Products: Stereochemistry
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Diels–Alder Reaction: Characteristics of Dienes
Characteristics of the diene
Conformation
The simplest example of a diene is 1,3-butadiene, an acyclic conjugated π system. At room temperature, the molecule exists as a mixture of s-cis and s-trans conformers by virtue of rotation around the carbon–carbon single bond. Although the s-trans isomer is...
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry