Cyclic polylactide synthesis initiated by a lithium anthraquinoid: understanding the selectivity through DFT and diffusion NMR

• Published in: Polymer chemistry 2021-07, Vol.12 (28), p.483-492
• Main Authors: Martínez, Cristina Ruiz, Pérez, Juana M, Arrabal-Campos, Francisco M, Batuecas, María, Ortuño, Manuel A, Fernández, Ignacio
• Format: Article
• Language: English
• Subjects: Algorithms; Catalysts; Diffusion; Dispersion; Drift; Ions; Laplace transforms; Lithium; Mass spectrometry; NMR; Nuclear magnetic resonance; Polylactic acid; Polymer chemistry; Room temperature; Selectivity; Spectra
• ISSN: 1759-9954; 1759-9962
• DOI: 10.1039/d1py00547b

We report herein the first lithium anthraquinoid catalyst able to produce polylactide at room temperature starting from both l - and rac -lactide in the absence of any other initiator. The new lithium-based system is selective towards cyclic polymers, having narrow dispersity and weight-average molecular weights ranging from 49.5 to 137.6 kDa. The cyclic structure of the PLA generated from the lithium catalyst has been determined by a combination of 1 H NMR and DRIFT spectroscopy techniques and MALDI-TOF mass spectrometry. DFT calculations point to lithium aggregation as the key feature of the catalyst controlling the linear : cyclic polymer ratio. Molar mass distributions and dispersities were obtained through diffusion NMR experiments combined with inverse Laplace transform algorithms and compared with those obtained by SEC as the most established method. We present herein the application of a lithium anthraquinoid in the catalytic synthesis of cyclic PLA, showing that the aggregation plays a critical role in cyclic vs. linear selectivity.