Journal
CHEMISTRY-A EUROPEAN JOURNAL
Volume 16, Issue 13, Pages 3983-3993Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.200903275
Keywords
fluorescence; N-heterocyclic carbenes; olefin metathesis; ring-closing metathesis; ruthenium
Categories
Funding
- DFG
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Imidazolium salts (NHCewg center dot HCl) with electronically variable substituents in the 4,5-position (H,H or Cl,Cl or H,NO2 or CN,CN) and sterically variable substituents in the 1,3-position (Me,Me or Et,Et or iPr,iPr or Me,iPr) were synthesized and converted into the respective [AgI(NHC)(ewg)] complexes. The reactions of [(NHC)RuCl2(CHPh)(py)(2)] with the [AgI(NHCewg)] complexes provide the respective [(NHC)(NHCewg)RuCl2(CHPh)] complexes in excellent yields. The catalytic activity of such complexes in ring-closing metathesis (RCM) reactions leading to tetrasubstituted olefins was studied. To obtain quantitative substrate conversion, catalyst loadings of 0.2-0.5 mol% at 80 degrees C in toluene are sufficient. The complex with the best catalytic activity in such RCM reactions and the fastest initiation rate has an NHCewg group with 1,3-Me,iPr and 4,5-Cl,Cl substituents and can be synthesized in 95% isolated yield from the ruthenium precursor. To learn which one of the two NHC ligands acts as the leaving group in olefin metathesis reactions two complexes, [(FL-NHC)-(NHCewg)RuCl2(CHPh)] and [(FL-NHCewg)(NHC)RuCl2(CHPh)], with a dansyl fluorophore (FL)-tagged electron-rich NHC ligand (FL-NHC) and an electron-deficient NHC ligand (FL-NHC) were prepared. The fluorescence of the dansyl fluorophore is quenched as long as it is in close vicinity to ruthenium, but increases strongly upon dissociation of the respective fluorophore-tagged ligand. In this manner, it was shown for ring-opening metathesis ploymerization (ROMP) reactions at room temperature that the NHCewg ligand normally acts as the leaving group, whereas the other NHC ligand remains ligated to ruthenium.
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