Abstract
Monopotassium dipropylene glycoxide, activated by a 18-crown-6 cation complexing agent (K-DPG/L, where DPG (dipropylene glycol) is a mixture of isomers) was used as an effective initiator of the homopolymerization and copolymerization of several monosubstituted oxiranes, i.e., propylene oxide (PO), 1.2-butylene oxide (BO), and some glycidyl ethers such as allyl, isopropyl, phenyl, and benzyl ones (AGE, IPGE, PGE, and BGE, respectively). The copolymers are novel and can be prospectively used for the fabrication of new thermoplastic or crosslinked polyurethanes. All processes were carried out in homogeneous mild conditions, i.e., tetrahydrofuran solution at room temperature and normal pressure. They resulted in new unimodal macrodiols with Mn = Mcalc in the range of 1500-8300, low dispersity Mw/Mn = 1.08-1.18 and a chemical structure well defined by several techniques, i.e., MALDI-TOF, size exclusion chromatography (SEC), 13C NMR, and FTIR. Monopotassium salts of homopolyether-diols, i.e., PPO-diol, PBO-diol, and PAGE-diol, appeared to be useful macroinitiators for the preparation of new triblock copolyether-diols by polymerization of glycidyl ethers. In BO/BGE random copolymerization initiated with K-DPG/L, macromolecules of copolyether-diol were exclusively formed. Macromolecules of copolyether-diol accompanied by homopolyether PPO-diol were identified in the PO/PGE system. However, AGE and PGE reacted by giving random copolyether-diol as well as homopolymer-diols, i.e., PAGE-diol and PPGE-diol. Macromolecules of prepared copolyether-diols contain various numbers of mers deriving from comonomers; the kind of comonomer determines the composition of the product. Several prepared homopolyether-diols and copolyether-diols could be useful for the synthesis of new thermoplastic polyurethanes.