New Polymer Syntheses. 100. Multiblock Copolyesters by Combined Macrocyclic Polymerization and Silicon-Mediated Polycondensation

• Published in: Macromolecules 1998-09, Vol.31 (19), p.6403-6408
• Main Authors: Kricheldorf, Hans R, Eggerstedt, Sven
• Format: Article
• Language: English
• Subjects: Applied sciences; Exact sciences and technology; Organic polymers; Physicochemistry of polymers; Polymers with particular structures; Preparation, kinetics, thermodynamics, mechanism and catalysts
• ISSN: 0024-9297; 1520-5835
• DOI: 10.1021/ma980246c

Using 2,2-dibutyl-2-stanna-1,3-dioxepane (DSDOP) as cyclic initiator the macrocyclic polymerizations of ε-caprolactone were conducted in bulk at 80 °C at monomer/initiator ratios of 20/1. The resulting tin-containing supermacrocycles were reacted in situ with an excess of isophthaloyl chloride, and this reaction mixture was polycondensed with silylated Bisphenol A at temperatures between 150 and 300 °C. The characterization of the isolated copolyesters by DSC measurements and 1H NMR and 13C NMR spectroscopy proved that they possess a perfect multiblock structure up to a reaction temperature of 240 °C. At higher temperatures transesterification causes a more or less perfect randomization of the sequence. In a second series of combined ring-opening polymerizations and ring-opening polycondensations (ROPPOC) silylated methylhydroquinone and 1,10-bis(4-chlorophenoxy)decane were used as comonomers of the macrocyclic poly(ε-caprolactone). The isolated multiblock copolyesters showed a two phasic melt with an isotropic phase containing the polylactone blocks and a nematic phase consisting of the aromatic blocks. The relationship between block lengths and phase separation is discussed.