dc.creator |
Yu, Baoyi |
|
dc.creator |
Hamad, Fatma B. |
|
dc.creator |
Sels, Bert |
|
dc.creator |
Van Hecke, Kristof |
|
dc.creator |
Verpoort, Francis |
|
dc.date |
2016-06-18T18:16:06Z |
|
dc.date |
2016-06-18T18:16:06Z |
|
dc.date |
2015 |
|
dc.date.accessioned |
2018-03-27T08:54:33Z |
|
dc.date.available |
2018-03-27T08:54:33Z |
|
dc.identifier |
Yu, B., Hamad, F.B., Sels, B., Van Hecke, K. and Verpoort, F., 2015. Ruthenium indenylidene complexes bearing N-alkyl/N-mesityl-substituted N-heterocyclic carbene ligands. Dalton Transactions, 44(26), pp.11835-11842. |
|
dc.identifier |
http://hdl.handle.net/20.500.11810/2585 |
|
dc.identifier |
10.1039/c5dt00967g |
|
dc.identifier.uri |
http://hdl.handle.net/20.500.11810/2585 |
|
dc.description |
We report on the synthesis and characterization of second generation ruthenium indenylidene catalysts bearing unsymmetrical N-heterocyclic carbene (NHC) ligands denoted as RuCl2(3-phenyl-1-indenylidene)(1-mesityl-3-R-4,5-dihydroimidazol-2-ylidene)(PCy3), in which R is methyl , octyl or cyclohexyl . The characterization of was performed by NMR spectroscopy, elemental analysis, IR, HRMS and single-crystal X-ray diffraction analysis. In addition, the catalytic activity of the obtained initiators was evaluated in various representative metathesis reactions. The results reveal that the complexes , bearing an N-alkyl side on the NHC, show a faster catalytic initiation than the reference complex . Complex , which performs the best among the investigated indenylidene complexes, exhibits slower initiation but better overall efficiency than its benzylidene analogue , especially in a low catalyst loading. |
|
dc.language |
en |
|
dc.title |
Ruthenium Indenylidene Complexes Bearing N-Alkyl/N-Mesityl-Substituted N-Heterocyclic Carbene Ligands |
|
dc.type |
Journal Article, Peer Reviewed |
|