Abstract
The zinc complex Zn(C6F5)2(toluene) (1) behaves as a very active and selective catalyst in cyclohexene oxide (CHO) polymerization to produce poly(cyclohexene oxide) (PCHO) by the trans-ring-opening of CHO with remarkable TOF values at room temperature. The ring-opening copolymerization (ROCOP) of CO2 with CHO catalysed by 1 yields poly(cyclohexene carbonate) (PCHC) when using benzyl alcohol (BnOH) as an initiator at 120 °C. The 1H NMR monitoring of the in situ reaction of 1 with BnOH highlighted the formation of the dinuclear species [(C6F5)2Zn2(BnO)2 (2) that was isolated and found an active catalyst in the ROCOP of CO2 with CHO in the absence of initiators. Interestingly, PCHCs by 2 in solventless conditions show polydispersity index (Mw/Mn) values close to 2, corresponding to those expected for a single-site catalyst; on the contrary, a broader polydispersity index of the polymer products was found in toluene solution, suggesting the formation of new zinc catalysts during the polymerization reaction.
Subject
Physical and Theoretical Chemistry,Catalysis,General Environmental Science
Cited by
2 articles.
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