Novel initiators for the synthesis of propylene oxide oligomers by anionic ring opening polymerization

• Published in: Catalysis today 2008-01, Vol.130 (2), p.486-491
• Main Authors: Cendejas, Gabriel, Arreguín, Felipe, Flores, César, Villalobos, Iván, Flores, Eugenio, Vázquez, Flavio
• Format: Article
• Language: English
• Subjects: Alkoxides; Anionic ring opening polymerization (AROP); Catalysis; Chemistry; Exact sciences and technology; FTIR; General and physical chemistry; Initiator; NMR; Oligomers; Propylene oxide; Quantum semiempirical calculations; SEC; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
• ISSN: 0920-5861; 1873-4308
• DOI: 10.1016/j.cattod.2007.10.107

A series of potassium alcoholates was obtained from the reaction between KOH and ethylene glycol, resorcinol, 4,4′-bisphenol A, 4,4′-(1,3 phenylenediisopropylidene)-bisphenol, 4,4′-sulfonyldiphenol. These salts were employed to initiate the anionic ring opening polymerization of propylene oxide (PO). The molecular weight distribution of the propylene oxide oligomers prepared by this method and the initiator structure were correlated. These oligomers were characterized through Fourier transform infrared (FTIR), nuclear magnetic resonance (NMR) spectroscopies and size exclusion chromatography (SEC). It was found that the molecular weight and polydispersity of the synthesized poly(propylene oxide) (PPO) is highly dependant on the initiator structure and solubility in the reactive medium. The oligomers obtained using di-potassium resorcinolate exhibited a molecular weight distribution more polydisperse than that of PO oligomers synthesized by means of di-potassium ethylene glycolate. In the case of the PO polymerizations started by the potassium salts of 4,4′-bisphenol A, 4,4′-(1,3 phenylenediisopropylidene)-bisphenol and 4,4′-sulfonyldiphenol, the oligomer chains showed very broad molecular weight distributions. In general, lower solubility and augmentation of the polymer polydispersity were observed when the number of aromatic rings in the initiator structure increased. The experimental results were contrasted with those obtained from quantum chemical semiempirical calculations at AM1 level. The peculiar behavior exhibited by the initiators with an aromatic structure could be explained in terms of different reactivities of the initiation sites. The theoretical studies revealed that the ring in the aromatic initiators promotes an unsymmetrical growing when the PPO chains are formed. In contrast, the identical reactivity of both initiation sites in the ethylene glycolate produces a symmetrical growing during the PO polymerization.