Dedicated to Professor Thomas P. Fehlner on the occasion of his 65th birthday, in recognition of his outstanding contributions to organometallic and inorganic chemistry.
Research Article
Bi- and tri-metallic {Cp*RhCl} fragments partnered with carborane monoanions [CB11H6Y6]− (Y = H, Br): control of nuclearity by choice of anion†
Article first published online: 7 MAY 2003
DOI: 10.1002/aoc.440
Copyright © 2003 John Wiley & Sons, Ltd.
Issue
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Applied Organometallic Chemistry
Special Issue: Dedicated to Professor Thomas P. Fehlner on the occasion of his 65th birthday
Volume 17, Issue 6-7, pages 388–392, June - July 2003
Additional Information
How to Cite
Patmore, N. J., Mahon, M. F. and Weller, A. S. (2003), Bi- and tri-metallic {Cp*RhCl} fragments partnered with carborane monoanions [CB11H6Y6]− (Y = H, Br): control of nuclearity by choice of anion. Appl. Organometal. Chem., 17: 388–392. doi: 10.1002/aoc.440
- †
Publication History
- Issue published online: 7 MAY 2003
- Article first published online: 7 MAY 2003
- Manuscript Accepted: 24 JAN 2003
- Manuscript Revised: 6 JAN 2003
- Manuscript Received: 11 DEC 2002
Funded by
- Royal Society.
- Abstract
- References
- Cited By
Keywords:
- carborane;
- weakly coordinating;
- rhodium;
- hydrogen bond
Abstract
Reaction of [Cp*RhCl2]2 (Cp* = pentamethylcyclopentadienyl) with Ag[closo-CB11H12] affords the dinuclear salt [Cp*RhCl]2[CB11H12]2 (1), which in the solid state reveals a single carborane anion interacting with two {Cp*RhCl} fragments, via two B
H
Rh interactions. With Ag[closo-CB11H6Br6] the trimetallic complex [{Cp*Rh(µ2-Cl)} 3(µ3-Cl)][closo-CB11H6Br6]2 (2) results. In the solid state, three metal fragments and four chloride ligands form seven-corners of a cube, and the eighth vertex is completed by a cage C
H unit hydrogen bonded to three bridging chloride ligands. Copyright © 2003 John Wiley & Sons, Ltd.

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