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- URN to cite this document:
- urn:nbn:de:bvb:355-epub-354000
- DOI to cite this document:
- 10.5283/epub.35400
Abstract
Hydrogen bonding plays a crucial role in Bronsted acid catalysis. However, the hydrogen bond properties responsible for the activation of the substrate are still under debate. Here, we report an in depth study of the properties and geometries of the hydrogen bonds in (R)-TRIP imine complexes (TRIP: 3,3'-Bis(2,4,6-triisopropylphenyl)-1,1'-binaphthyl-2,2'-diylhydrogen phosphate). From NMR ...

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