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Ring‐expansion polymerization of meso‐lactide catalyzed by dibutyltin derivatives
Abstract:Meso‐Lactide was polymerized in bulk at 60, 80, and 100 °C by means of three different types of catalysts: dibutyltin sulfides (2,2‐dibutyl‐2‐stanna‐1,3‐dithiolane and 2,2′‐dibutyl‐2‐stanna‐1,3‐dithiane), dibutyltin derivatives of substituted catechols (BuCa, CyCa, and BzCa), and dibutyltin derivatives of 2,2′dihydroxybiphenyl (SnBi) and 2,2′‐dihydroxy‐1,1′‐binaphthyl (SnNa). Only the latter two catalysts were active at 60 °C. The architecture of the resulting polylactides depends very much on the structure of the catalyst and on the temperature. At the lowest temperature (60 °C), SnBi and SnNa mainly yielded even‐numbered linear chains, but SnNa also yielded even‐numbered cycles at 100 °C and short reaction times. In contrast, BuCa, CyCa, and BzCa mainly yielded odd‐numbered cycles, although the same catalysts yielded even‐numbered linear chains when benzylalcohol was added. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 749–759
Keywords:cyclization  catalysts  matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry (MALDI‐TOF MS)  polyester  polymerization
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