About Polycondensation, Disproportionation, and Cyclization of Acetylated Poly(L‐Lactide) Esters

Author:

Kricheldorf Hans R.1ORCID,Weidner Steffen M.2,Meyer Andreas3

Affiliation:

1. Institut für Technische und Makromolekulare Chemie Universität Hamburg Bundesstraße 45 D‐20146 Hamburg Germany

2. Bundesanstalt für Materialforschung und ‐prüfung Richard Willstätter Str. 11 D‐12489 Berlin Germany

3. Institut für Physikalische Chemie Universität Hamburg Grindelallee 117 D‐20146 Hamburg Germany

Abstract

AbstractL‐lactide (LA) is polymerized with ethyl L‐lactate or trifluoroethanol as initiators (LA/In = 30/1), and the resulting poly(L‐lactide) esters are acetylated with acetic anhydride. The acetylated PLA esters are mixed with SnOct2, dibutyltin bis(4‐chlorophenoxide), or dibutyltin bis(pentafluorophenoxide) in solution and crystallized at 120 °C. The doped crystals are annealed at 140 °C or at 160 °C for 7, 14, and 28 days, and the chemical modifications that occurred in the solid state are monitored by matrix‐assisted laser desorption/ionization time‐of‐flight (MALDI TOF) mass spectrometry, gel permeation chromatography (GPC), and differential scanning calorimetry (DSC) measurements. All catalysts promoted polycondensation, while no significant formation of cycles is observed. However, in the presence of SnOct2, disproportionation of chains occurred upon annealing at 120 or 140 °C, and crystallites consisting of extended chains with Mn values ≈3500 – 3600 and low dispersities (Ð < 1.5) are formed.

Publisher

Wiley

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