http://www.cnr.it/ontology/cnr/individuo/prodotto/ID272694
Tethered ansa-bridged titanium complexes immobilized on 3-mercaptopropyl-functionalized silica gel and their application for the hydrosilylation of imines (Articolo in rivista)
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- Tethered ansa-bridged titanium complexes immobilized on 3-mercaptopropyl-functionalized silica gel and their application for the hydrosilylation of imines (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/c2dt31207g (literal)
- Alternative label
Gruber-Wölfler H., Neubauer C., Lichtenegger G.J., Polo E., Khinast J. (2012)
Tethered ansa-bridged titanium complexes immobilized on 3-mercaptopropyl-functionalized silica gel and their application for the hydrosilylation of imines
in Dalton transactions (2003. Print); ROYAL SOC CHEMISTRY, THOMAS GRAHAM HOUSE,, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND (Regno Unito)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Gruber-Wölfler H., Neubauer C., Lichtenegger G.J., Polo E., Khinast J. (literal)
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- http://pubs.rsc.org/en/content/articlepdf/2012/DT/C2DT31207G (literal)
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Gruber-Wölfler H., Neubauer C., Lichtenegger G.J., Khinast J., Graz Univ Technol, Inst Proc & Particle Engn,
Polo E., ISOF - ISOF - Ferrara (literal)
- Titolo
- Tethered ansa-bridged titanium complexes immobilized on 3-mercaptopropyl-functionalized silica gel and their application for the hydrosilylation of imines (literal)
- Abstract
- Four tethered titanocene complexes were covalently immobilized onto 3-mercaptopropyl-functionalized silica gel. We have investigated the influence of the length of the tether and of the ansa-bridge on the activity in the heterogeneous hydrosilylation of the cyclic imine 2-phenylpyrroline, taken as an illustrative example. Possible metal leaching during the reaction was investigated using ICP/OES, recycling studies and the three-phase test. The novel immobilized catalysts exhibit an activity similar to their homogeneous analogues in the tested hydrosilylation reactions with a TOF of similar to 20 h(-1). Furthermore, our results indicate that metal leaching is negligible under the applied reaction conditions (literal)
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