CIS/TRANS COORDINATION IN OLEFIN METATHESIS BY STATIC AND MOLECULAR DYNAMIC DFT CALCULATIONS

Abstract

In regard to [(N-heterocyclic carbene)Ru]-based catalysts, it is still a matter of debate if the substrate binding is preferentially cis or trans to the N-heterocyclic carbene ligand. By means of static and molecular dynamic DFT calculations a simple olefin, like ethylene, is shown to be prone to the trans binding. Bearing in mind the higher reactivity of trans isomers in olefin metathesis this insight helps to construct small alkene substrates with
increased reactivity.

How to Cite
Poater, A.; Correa, A.; Pump, E.; Cavallo, L. Chem. Heterocycl. Compd. 2014, 50, 389. [Khim. Geterotsikl. Soedin. 2014, 424.]

For this article in the English edition see DOI 10.1007/s10593-014-1491-6