Related Experiment Video
Updated: Apr 16, 2026

Coulomb Explosion Imaging as a Tool to Distinguish Between Stereoisomers
Published on: August 18, 2017
Perspective: Vibrational-induced steric effects in bimolecular reactions
1Institute of Atomic and Molecular Sciences (IAMS), Academia Sinica, P.O. Box 23-166, Taipei 10617, Taiwan.
Understanding collision geometry in bimolecular reactions is key. Studies on excited CHD3 with F, Cl, and O atoms reveal passive and active steric control, influencing chemical reactivity through anisotropic interactions and laser polarization.
Area of Science:
- Chemical Dynamics
- Molecular Reaction Mechanisms
- Spectroscopy
Background:
- Collision geometry significantly influences bimolecular reaction outcomes.
- Steric control is a critical factor in directing chemical reactivity.
- Understanding these effects is crucial for controlling chemical reactions.
Purpose of the Study:
- To investigate the role of preferred collision geometry in bimolecular reactions.
- To highlight two types of steric control: passive and active.
- To examine the influence of anisotropic interactions and laser polarization on reactivity.
Main Methods:
- Crossed molecular beam studies on C-H stretch-excited CHD3(v1 = 1) reactions.
- Investigated reactions with F, Cl, and O((3)P) atoms.
- Utilized infrared laser polarization for reactant alignment.
Main Results:
- Passive control observed in reactions with strong anisotropic entry valleys (F and O atoms).
- O((3)P) + CHD3(v1 = 1) showed enhanced reactivity due to funneling effects.
- Active control demonstrated in Cl + CHD3(v1 = 1) via laser-induced polarization.
Conclusions:
- Collision geometry and steric effects are crucial for controlling chemical reactivity.
- Anisotropic interactions can either inhibit (F) or enhance (O) reactions.
- Laser polarization offers a method for active steric control in reactions.
Related Concept Videos
Radical Reactivity: Steric Effects
Along with electronic...
Directing and Steric Effects in Disubstituted Benzene Derivatives
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Regioselectivity of Electrophilic Additions to Alkenes: Markovnikov's Rule
The hydrohalogenation of an unsymmetrical alkene can yield two haloalkane products, depending on which vinylic carbon takes up the halogen. However, one product usually predominates, where hydrogen adds to the vinylic carbon bearing the...
E1 Reaction: Stereochemistry and Regiochemistry

