A Unique Reaction Pathway of Fluorine-Substituted Ethyl Groups on Cu(111): Successive α,α-Fluoride Elimination
Author:
Affiliation:
1. Department of Chemistry, Center for Nanoscience and Nanotechnology, National Sun Yat-Sen University, Kaohsiung, Taiwan 80424, and National Synchrotron Radiation Research Center (NSRRC), Hsinchu, Taiwan 30077
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja047831f
Reference20 articles.
1. Structure, Reactivity, and Chemistry of Fluoroalkyl Radicals
2. Activation of Carbon-Fluorine Bonds by Metal Complexes
3. Fluorinated organometallics: Perfluoroalkyl and functionalized perfluoroalkyl organometallic reagents in organic synthesis
4. Preparation and reactivity of alkyl groups adsorbed on metal surfaces
5. Two-Dimensional Imaging of Reactively Desorbing CuF: State-Selective Angular and Velocity Distributions
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1. The Domino Multicomponent Allylation Reaction for the Stereoselective Synthesis of Homoallylic Alcohols;Accounts of Chemical Research;2009-01-20
2. Activation of Aromatic, Aliphatic, and Olefinic Carbon–Fluorine Bonds Using Cp* 2 HfH 2;European Journal of Inorganic Chemistry;2007-06
3. The chemistry of C2 perfluoroalkyl iodide on the Cu(111) single crystal surface;Surface Science;2007-01
4. Catalytic Activation of C–H and C–F Bonds in Alkyl Groups Adsorbed on Copper Surfaces: α- and β-Elimination Pathways;Science and Technology in Catalysis 2006;2007
5. Organic chemistry on solid surfaces;Surface Science Reports;2006-07
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