Deprotonation of indene–tricarbonylchromium with KH in tetrahydrofuran at –40 °C gives the η6-tricarbonylchromium–indenyl anion which reacts with [Rh(CI)COD]2(COD = cyclo-octa-1,5-diene) to form [η6-Cr(CO)3-indenyl-η3-rhodium-η4- COD]; the same bimetallic complex is obtained by reaction of the rhodium dimer with the isomeric η5-indenyl-tricarbonylchromium anion.
A. Ceccon, A. Gambaro, S. Santi, G. Valle and A. Venzo, J. Chem. Soc., Chem. Commun., 1989, 51 DOI: 10.1039/C39890000051
To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.
If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.
Read more about how to correctly acknowledge RSC content.
Please wait while we load your content...