scholarly journals Simple activation by acid of latent Ru-NHC-based metathesis initiators bearing 8-quinolinolate co-ligands

2016 ◽  
Vol 12 ◽  
pp. 154-165 ◽  
Author(s):  
Julia Wappel ◽  
Roland C Fischer ◽  
Luigi Cavallo ◽  
Christian Slugovc ◽  
Albert Poater

A straightforward synthesis utilizing the ring-opening metathesis polymerization (ROMP) reaction is described for acid-triggered N,O-chelating ruthenium-based pre-catalysts bearing one or two 8-quinolinolate ligands. The innovative pre-catalysts were tested regarding their behavior in ROMP and especially for their use in the synthesis of poly(dicyclopentadiene) (pDCPD). Bearing either the common phosphine leaving ligand in the first and second Grubbs olefin metathesis catalysts, or the Ru–O bond cleavage for the next Hoveyda-type catalysts, this work is a step forward towards the control of polymer functionalization and living or switchable polymerizations.

2007 ◽  
Vol 26 (26) ◽  
pp. 6515-6518 ◽  
Author(s):  
Adam N. Roberts ◽  
Alison C. Cochran ◽  
David A. Rankin ◽  
Andrew B. Lowe ◽  
Hans-Jörg Schanz

2013 ◽  
Vol 135 (27) ◽  
pp. 10032-10035 ◽  
Author(s):  
Lauren E. Rosebrugh ◽  
Vanessa M. Marx ◽  
Benjamin K. Keitz ◽  
Robert H. Grubbs

2019 ◽  
Vol 15 ◽  
pp. 310-332 ◽  
Author(s):  
Patrycja Żak ◽  
Cezary Pietraszuk

This mini-review summarizes the applications of olefin metathesis in synthesis and functionalization of polyhedral oligomeric silsesquioxanes (POSS) and POSS-containing polymeric materials. Three types of processes, i.e., cross metathesis (CM) of vinyl-substituted POSS with terminal olefins, acyclic diene metathesis (ADMET) copolymerization of divinyl-substituted POSS with α,ω-dienes and ring-opening metathesis polymerization (ROMP) of POSS-substituted norbornene (or other ROMP susceptible cycloolefins) are discussed. Emphasis was put on the synthetic and catalytic aspects rather than on the properties and applications of synthesized materials.


2021 ◽  
Vol 2131 (4) ◽  
pp. 042055
Author(s):  
Huanhuan Zhao ◽  
Yanwu Zhang

Abstract The tri-block copolymer is used as a carrier to simultaneously immobilize the N-heterocyclic and benzylidene ligands precursor of the Ru-based catalyst to form a dual-site immobilized catalyst. The dual-site immobilized catalyst can catalyze ring-opening metathesis polymerization, ring-closing metathesis and self-metathesis. The dual-site immobilized catalyst shows good heterogeneity in dichloromethane, which simplifies the purification of product and recovery of catalyst. The dual-site immobilized catalyst exhibits excellent activity and recycling performance. The excellent recyclability can be attributed to the capture of ruthenium by the excess ligands precursor on carrier. Importantly, ruthenium residues are not detected in product.


2015 ◽  
Vol 44 (4) ◽  
pp. 1724-1733 ◽  
Author(s):  
Fatme Dahcheh ◽  
Douglas W. Stephan

A series of bis-carbene Ru-hydride species were prepared and subsequently shown to react with aryl-vinyl-sulfides to give the corresponding biscarbene-alkylidene complexes. The activities of these species for ring-opening metathesis polymerization, ring-closing and cross-metathesis are reported. While these systems are shown to exhibit modest metathesis activities, the reactivity is enhanced in the presence of BCl3.


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