Remote Functionalization of Carbon-Hydrogen and Carbon-Carbon Bonds by Bare Transition Metal Ions in the Gas Phase
- 1 January 1989
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- The coordination of bare iron(I) ion (Fe+) to aliphatic isonitriles differs from that of Fe+ and nitrilesJournal of the American Chemical Society, 1988
- The reaction of linear nitriles with transition metal ions M+ (M = Fe, Co, Ni) in the gas phase. Does the back-bonding ability of the metal ions govern the geometry of the RCN/M+ complexes and what is the effect on the oxidative addition of internal CH bonds?International Journal of Mass Spectrometry and Ion Processes, 1987
- Only the copper(I) ion coordinated to the .pi.-system of the nitrile group activates upon collision carbon-hydrogen and carbon-carbon bonds of nitrilesOrganometallics, 1987
- Deceptive similarities in the reactions of iron(I) and cobalt(I) with linear nitriles in the gas phaseJournal of the American Chemical Society, 1987
- Fast atom bombardment as a convenient means to generate metal ion complexes in the gas phaseInternational Journal of Mass Spectrometry and Ion Processes, 1987
- On the mechanism of Fe+-induced hydrogen migrations in gaseous octyne/iron(I) complexesJournal of the American Chemical Society, 1987
- Reaction of nitriles and iron(1+) in the gas phase. A case of remote functionalizationJournal of the American Chemical Society, 1987
- Carbon-hydrogen and hydrogen-hydrogen activation in transition metal complexes and on surfacesJournal of the American Chemical Society, 1984
- .beta.-Alkyl transfer in a lanthanide model for chain terminationJournal of the American Chemical Society, 1982
- Collision SpectroscopyPublished by Springer Nature ,1978