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Polyester polyols synthesized via a polycondensation reaction of diols with diacids or their diesters are commonly used as polyurethane building blocks. Herein, we demonstrate an alternative route to polyester polyols via oxidative esterification of aliphatic α,ω-diols. Unlike the polycondensation reaction, this process is carried out in aqueous media at 30 °C under atmospheric pressure. In situ generated hypobromous acid from the mixture of NaBr, NaBrO3 and H2SO4 is used to trigger the reaction. The reaction progress can be conveniently controlled with the Br/OH molar ratio. The properties of the obtained polyesters are determined by the applied diol and can be tailored using a mixture of diols. The composition of polymers is determined with GPC, NMR, and MALDI-TOF MS. It is shown that polyesters obtained with this method can be used as precursors for polyurethane synthesis. This work provides a quick and convenient route to polyester polyol synthesis, feasible in any laboratory.

In this study, we report the synthesis and phase behaviour of statistical p(N-isopropylacrylamide-co-2-acrylamidephenylboronic acid) P(NIPAM-co-2-AAPBA) copolymers. They were obtained via free radical copolymerization of NIPAM and the pinacol ester of 2-acrylamidephenylboronic acid. The influence of copolymer composition on the demixing/mixing temperature was investigated by means of UV/Vis spectrometry, DLS, DSC, and 1H NMR spectroscopy. The turbidity experiments revealed the gradual increase of the cloud point with the increase of 2-AAPBA content in the copolymer up to 37 °C at 30 mol%. The copolymer with 45 mol% did not display any transition. For copolymers displaying the cloud point, the hysteresis in the demixing/mixing temperature was observed. Transmittance measurements, DLS, and 1H NMR spectroscopy demonstrated that the phase transition was sharp upon heating, whereas the phase transition of the copolymer upon a decrease of temperature occurred in a much wider temperature range. Moreover, the NIPAM copolymer with 5 mol% 2-AAPBA content displayed 5 °C hysteresis, whereas for the copolymer containing 30 mol% 2-AAPBA it reached 25 °C. Actually, nanoparticles were formed from the copolymer with 30 mol% of 2-AAPBA above the cloud point, which were stable upon cooling to 5 °C showing the potential for drug delivery applications. Raman spectroscopy applied for the analysis of an aqueous solution of NIPAM copolymer with 15 mol% content heated over the cloud point revealed the appearance of a vibrational band at 753 cm−1 characteristic of boroxine, i.e., boronic acid anhydride, the formation of which explains the broadening of the hysteresis. The detailed analysis of experimental data supported with DFT calculations evidenced the presence of other vibrational bands of 2-AAPBA anhydride (780, 957 and 999 cm−1). This is the first report of boroxine formation upon the phase transition of boronic acid-based thermoresponsive copolymers.