Exploration of reactional parameters for palladium-catalyzed cross-coupling reaction with thermal
Min-Zong Huang1, Yan-Jyun Huang1, Wenjian Sun2
1Department of Chemistry, National Sun Yat-Sen University, 804, Kaohsiung, Taiwan.
Abstract:
Thermal desorption-electrospray ionization/mass spectrometry (TD-ESI/MS), an ambient ionization mass spectrometric technique, was used to explore reactional parameters of a palladium-catalyzed cross-coupling reaction. TD-ESI/MS employed a thermal desorption unit to convert analytes from solution to gas phase. After which, the desorbed analytes reacted with the charged solvent species in an electrospray plume to form analyte ions prior to mass spectrometric detection. Since analytes are separated from the matrix before ionization, the composition of sample matrix will not affect the ionization efficiency of the analyte. With its simple sampling, easy operation, minimal sample preparation requirements, and rapid analytical workflow, TD-ESI/MS shows significant promise for rapid qualitative analysis and characterization of chemical compounds in ongoing chemical reactions. The time-resolved mass spectra provided detailed insights into the changes of chemical species throughout the reaction. This approach enables comprehensive exploration of the parameters involved in the reaction mechanisms, including the impacts of various reactional factors such as solvent type, electron-withdrawing or electron-donating group on the reactants, and substituent position of the reactants.
More Related Videos
Related Concept Videos
Tandem Mass Spectrometry
Cycloaddition Reactions: MO Requirements for Thermal Activation
Electrospray Ionization (ESI) Mass Spectrometry
ESI utilizes electrical energy to transfer ions from the liquid phase of the sample into the...
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Mass Spectrometry: Cycloalkene Fragmentation
![Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F51444.jpg&w=3840&q=50)

