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The Influence of C(sp<sup>3</sup>)H–Selenium Interactions on the <sup>77</sup>Se NMR Quantification of the π‐Accepting Properties of Carbenes

Glen P. Junor, Jan Lorkowski, Cory M. Weinstein, Rodolphe Jazzar, Cezary Pietraszuk, Guy Bertrand

2020Angewandte Chemie37 citationsDOIOpen Access PDF

Abstract

Abstract Selenium NMR has become a standard tool for scaling the π‐accepting character of carbenes. Herein, we highlight that non‐classical hydrogen bonding (NCHB), likely resulting from hyperconjugation, can play a significant role in the carbene–selenium 77 Se NMR chemical shift, thus triggering a non‐linear behavior of the Se‐Scale.

Topics & Concepts

SeleniumHyperconjugationChemistryCarbeneScalingComputational chemistryHydrogen bondMoleculeOrganic chemistryCatalysisMathematicsGeometryCyclopropane Reaction MechanismsN-Heterocyclic Carbenes in Organic and Inorganic ChemistryCoordination Chemistry and Organometallics
The Influence of C(sp<sup>3</sup>)H–Selenium Interactions on the <sup>77</sup>Se NMR Quantification of the π‐Accepting Properties of Carbenes | Litcius