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Updated: Aug 14, 2026

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
New experiments on HNCSe and HCNSe radical cations
P Gerbaux1, N Dechamps, R Flammang
1Laboratory of Organic Chemistry and Center of Mass Spectrometry, University of Mons-Hainaut, Avenue Maistriau 19, B-7000 Mons, Belgium.
Dissociative ionization of selenourea produces isocyanoselenic acid radical cations. Their connectivity was confirmed using mass spectrometry and ion-molecule reactions.
Area of Science:
- Chemical Physics
- Mass Spectrometry
- Organic Chemistry
Background:
- Isocyanoselenic acid radical cations (HNCSe(.+)) are important reactive intermediates.
- Previous methods for generating and characterizing these species have limitations.
Purpose of the Study:
- To develop a convenient method for generating pure isocyanoselenic acid radical cations.
- To confirm the HNCSe(.+) connectivity using advanced mass spectrometry techniques.
Main Methods:
- Dissociative ionization of selenourea (Se=C(NH(2))(2)) was employed for ion generation.
- Collisional activation and associative ion-molecule reactions were utilized for structural elucidation.
- A large-scale hybrid mass spectrometer was used for the experiments.
Main Results:
- Beams of pure isocyanoselenic acid radical cations were successfully generated.
- The HNCSe(.+) connectivity was unequivocally established through the applied methods.
- Reactions with dimethyl sulfide and nitric oxide provided further confirmation.
Conclusions:
- Dissociative ionization of selenourea is an efficient route to HNCSe(.+) ions.
- The established connectivity provides a foundation for further studies of these selenium-containing species.
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