Journal
NEW JOURNAL OF CHEMISTRY
Volume 41, Issue 15, Pages 6995-7006Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7nj01079f
Keywords
-
Categories
Funding
- German research foundation DFG within the transregional collaborative research centre [SFB/TRR 88]
- state research centre OPTIMAS
- research college MAGNENZ
- state research unit NanoKat
- Carl Zeiss Stiftung
Ask authors/readers for more resources
A set of cationic group IX metal complexes of the type [(eta(5)-Cp*) M(Cl)(N,N ')](+) bearing N,N '-coordinating ligands structurally related to 2,2 '-bipyridine were synthesized and characterized by means of elemental analysis, spectroscopy and single crystal X-ray diffraction. These complexes can undergo two different modes of CH activation in the gas phase, which were examined by CID ESI-MS spectrometry and by DFT calculations. On one hand, a roll-over cyclometallation can occur at one of the aromatic rings of the N,N '-coordinated ligands. On the other hand, a deprotonation of one of the Cp* methyl groups can take place, leading to complexes in the oxidation state +I with a tetramethylfulvene ligand coordinated. In both cases, the chlorido ligand acts as an internal base in the ESI-MS CID experiment.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available