“…While the industrial catalysts are usually heterogenous, academic ROMP research has focused on molecular single-component catalysts with metal-carbene complexes featuring prominently. Examples are tungsten-(carbene) complexes [3][4][5][6][7][8][9][10], molybdenum-(carbene) complexes [11][12][13][14][15][16][17] and ruthenium-(carbene) complexes [18][19][20][21][22][23][24]. The possibility of a ring-opening metathesis polymerization of norbornene with catalyst systems based on titanium [25], zirconium and hafnium [26], vanadium [27,28], niobium [29], tantalum [29][30][31][32], osmium [33] and rhenium [34] has been reported.…”
“…While the industrial catalysts are usually heterogenous, academic ROMP research has focused on molecular single-component catalysts with metal-carbene complexes featuring prominently. Examples are tungsten-(carbene) complexes [3][4][5][6][7][8][9][10], molybdenum-(carbene) complexes [11][12][13][14][15][16][17] and ruthenium-(carbene) complexes [18][19][20][21][22][23][24]. The possibility of a ring-opening metathesis polymerization of norbornene with catalyst systems based on titanium [25], zirconium and hafnium [26], vanadium [27,28], niobium [29], tantalum [29][30][31][32], osmium [33] and rhenium [34] has been reported.…”
“…The Grubbs-class ruthenium metathesis catalysts, while less sensitive to oxygen or water than the group 6 systems, are nevertheless susceptible to deactivation through chelation of (e.g.) carbonyl functionalities [76][77][78][79]. Instances of sensitivity to alcohol or amine functionalities have also been reported [80,81] (see also Section 4.1.2).…”
Section: Limitations On Reversibility In Rcm Reactionsmentioning
Synthesis of medium-sized and macrocyclic rings by ring closing metathesis (RCM) reactions of dienes involves challenges not found in synthesis of the more common five-and six-membered rings. This review discusses factors that determine the probability and efficiency of cyclization, and experimental methods that have been used to increase selectivity for RCM products, with specific reference to the concentrations at which RCM can be achieved. These issues have important implications for the environmental and economic sustainability of large-scale synthetic processes utilizing RCM for assembly of rings larger than six members.
“…Although analysis of the 1 H NMR spectra for the kinetic studies of the ROMP reactions initiated by well-defined ruthenium catalysts was extensively discussed in many publications [28][29][30][31][32], there are only few reports concerning analogous research of alkyne polymerization reactions [19][20][21]. Investigation of polymerization of 1,6-heptadiynes containing hydroxymethyl and ester groups with well-defined Ru-based initiators, i.e.…”
Section: Polymerization Of Hydroxyacetylenes In Nmr Tubementioning
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