Your browser doesn't support javascript.
loading
Steric Engineering of Rotaxane Catalysts: Benefits and Limits of Using the Mechanical Bond in Catalyst Design.
Struth, F Robin; Jansen, Dennis; Pairault, Noël; Schumacher, Marcel; Uteschil, Florian; Linders, Jürgen; Mayer, Christian; Gröschel, André H; Goldup, Stephen M; Niemeyer, Jochen.
Affiliation
  • Struth FR; Faculty of Chemistry (Organic Chemistry) and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Universitätsstrasse 7, 45141, Essen, Germany.
  • Jansen D; Faculty of Chemistry (Organic Chemistry) and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Universitätsstrasse 7, 45141, Essen, Germany.
  • Pairault N; Institut des Sciences Moléculaires (ISM), CNRS UMR 5255, University of Bordeaux, 33400, Talence, France.
  • Schumacher M; Institute of Organic Chemistry and Center for Soft Nanoscience (SoN), University of Muenster, Busso-Peus-Strasse 10, 48149, Muenster, Germany.
  • Uteschil F; Faculty of Chemistry (Organic Chemistry) and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Universitätsstrasse 7, 45141, Essen, Germany.
  • Linders J; Faculty of Chemistry (Physical Chemistry) and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Universitätsstrasse 7, 45141, Essen, Germany.
  • Mayer C; Faculty of Chemistry (Physical Chemistry) and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Universitätsstrasse 7, 45141, Essen, Germany.
  • Gröschel AH; Macromolecular Chemistry and Bavarian Centre for Battery Technology (BayBatt), University of Bayreuth, Weiherstrasse 26, 95448, Bayreuth, Germany.
  • Goldup SM; School of Chemistry, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
  • Niemeyer J; Faculty of Chemistry (Organic Chemistry) and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Universitätsstrasse 7, 45141, Essen, Germany.
Chemistry ; : e202402717, 2024 Aug 14.
Article in En | MEDLINE | ID: mdl-39140421
ABSTRACT
The mechanical bond is emerging as a novel design element in catalyst development. Here, we report a series of 1,1'-binaphthyl-2,2'-diol (BINOL) based catalysts in which the number of interlocked macrocycles is varied. Unsurprisingly, the macrocycles have a profound steric influence on the catalytic performance of these molecules. However, in the enantioselective transformations examined, the macrocycles are detrimental to catalyst stereoselectivity whereas in lactide polymerization, they increase the molecular weight of the polymeric product.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2024 Document type: Article Affiliation country: Germany Country of publication: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2024 Document type: Article Affiliation country: Germany Country of publication: Germany