| Literature DB >> 30758389 |
Pascal M Schäfer1, Paul McKeown, Martin Fuchs, Ruth D Rittinghaus, Alina Hermann, Johanna Henkel, Sebastian Seidel, Christoph Roitzheim, Agnieszka N Ksiazkiewicz, Alexander Hoffmann, Andrij Pich, Matthew D Jones, Sonja Herres-Pawlis.
Abstract
Non-toxic, highly active and robust complexes are the holy grail as ideal green catalysts for the polymerisation of biorenewable and biodegradable polylactide. Four new zinc guanidine complexes [ZnCl2(TMG4NMe2asme)], [ZnCl2(TMG5Clasme)], [ZnCl2(TMG5Measme)] and [ZnCl2(TMG5NMe2asme)] with different electron-donating and electron-withdrawing groups on the ligand's aromatic backbone have been synthesised. Ligands are derived from low-cost commercially available compounds and have been converted by a three- or four-step synthesis process into the desired ligand in good yields. The compounds have been fully characterised and tested in the ROP of rac-LA under industrially relevant conditions. The complexes are based on the recently published structure [ZnCl2(TMGasme)] which has shown high activity in the polymerisation of lactide at 150 °C. Different substituents in the para-position of the guanidine moiety significantly increase the polymerisation rate whereas positioning substituents in the meta-position causes no change in the reaction rate. With molecular weights over 71 000 g mol-1 being achievable, the best system produces polymers for multiple industrial applications and its polymerisation rate approaches that of Sn(Oct)2. The robust systems are able to polymerise non-purified lactide. The initiation of the polymerisation is suggested to occur due to impurities in the monomer.Entities:
Year: 2019 PMID: 30758389 DOI: 10.1039/c8dt04938f
Source DB: PubMed Journal: Dalton Trans ISSN: 1477-9226 Impact factor: 4.390