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Updated: Apr 25, 2026

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
Published on: October 18, 2019
N-heterocyclic carbene, high oxidation state molybdenum alkylidene complexes: functional-group-tolerant cationic
Michael R Buchmeiser1, Suman Sen, Jörg Unold
1Institut für Polymerchemie, Universität Stuttgart, Pfaffenwaldring 55, 70550 Stuttgart (Germany) http://www.uni-stuttgart.de/ipoc/msf/index_en.html. michael.buchmeiser@ipoc.uni-stuttgart.de.
Abstract:
We synthesized the first N-heterocyclic carbene (NHC) complexes of Schrock's molybdenum imido alkylidene bis(triflate) complexes. Unlike existing bis(triflate) complexes, the novel 16-electron complexes represent metathesis active, functional-group-tolerant catalysts. Single-crystal X-ray structures of two representatives of this novel class of Schrock catalysts are presented and reactivity is discussed in view of their structural peculiarities. In the presence of monomer (substrate), these catalysts form cationic species and can be employed in ring-closing metathesis (RCM), ring-opening metathesis polymerization (ROMP), as well as in the cyclopolymerization of α,ω-diynes. Monomers containing functional groups, which are not tolerated by the existing variations of Schrock's catalyst, e.g., sec-amine, hydroxy, and carboxylic acid moieties, can be used. These catalysts therefore hold great promise in both organic and polymer chemistry, where they allow for the use of protic monomers.
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