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Supported Ru olefin metathesis catalysts via a thiolate tether.
Renom-Carrasco, Marc; Mania, Philipp; Sayah, Reine; Veyre, Laurent; Occhipinti, Giovanni; Gajan, David; Lesage, Anne; Jensen, Vidar R; Thieuleux, Chloé.
Affiliation
  • Renom-Carrasco M; University of Lyon, Institute of Chemistry of Lyon, Laboratory C2P2 UMR 5265-CNRS-University Lyon 1-CPE Lyon, 43 Bd du 11 Novembre 1918, 69616 Villeurbanne, France. thieuleux@cpe.fr.
Dalton Trans ; 48(9): 2886-2890, 2019 Feb 26.
Article in En | MEDLINE | ID: mdl-30734797
Thiolate-coordinated ruthenium alkylidene complexes can give high Z-selectivity and stereoretentivity in olefin metathesis. To investigate their applicability as heterogeneous catalysts, we have successfully developed a methodology to easily immobilize prototype ruthenium alkylidenes onto hybrid mesostructured silica via a thiolate tether. In contrast, the preparation of the corresponding molecular complexes appeared very challenging in solution. These prototype supported complexes contain small thiolates but still, they are slightly more Z-selective than their molecular analogues. These results open the door to more active and selective heterogeneous catalysts by supporting more advanced thiolate Ru-complexes.

Full text: 1 Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2019 Type: Article Affiliation country: France

Full text: 1 Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2019 Type: Article Affiliation country: France