Abstract
The diyne complex [Cp*Ir(CO)(η2-ArC≡CC≡CAr)] reacts with two-electron donor ligands to form the iridacyclobutenone [Cp*Ir(L){C(C≡CAr)=C(Ar)C=O}]. Kinetic measurements and computational studies support the proposal that the reaction pathway involves alkyne insertion followed by coordination of the two-electron donor ligand.
Original language | English |
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Pages (from-to) | 4769-4773 |
Number of pages | 5 |
Journal | European Journal of Inorganic Chemistry |
Volume | 2016 |
Issue number | 29 |
DOIs | |
Publication status | Published - Oct 2016 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
ASJC Scopus Subject Areas
- Inorganic Chemistry
Keywords
- Cycloaddition
- Density functional calculations
- Diyne complexes
- Iridium
- Kinetics
- Metallacyclobutenone