a.Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, China
b.Faculty of Materials Science and Engineering, Qinghai University, Xining 810016, China
mszh.xin@qhu.edu.cn (H.X.Z.)
msjpzhao@scut.edu.cn (J.P.Z.)
收稿:2024-12-18,
修回:2025-01-15,
录用:2025-01-17,
网络首发:2025-03-04,
纸质出版:2025-05-20
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Pang, J.; Zhou, Y. B.; Liu, L. J.; Zhang, H. X.; Zhao, J. P. Ring-closing-opening copolymerization of phthalaldehyde and epoxide towards acid-degradable polyether and polyurethane. Chinese J. Polym. Sci. 2025, 43, 964–972
Jie Pang, Yu-Bo Zhou, Li-Jun Liu, et al. Ring-closing-opening Copolymerization of Phthalaldehyde and Epoxide towards Acid-degradable Polyether and Polyurethane[J]. Chinese Journal of Polymer Science, 2025, 43(6): 964-972.
Pang, J.; Zhou, Y. B.; Liu, L. J.; Zhang, H. X.; Zhao, J. P. Ring-closing-opening copolymerization of phthalaldehyde and epoxide towards acid-degradable polyether and polyurethane. Chinese J. Polym. Sci. 2025, 43, 964–972 DOI: 10.1007/s10118-025-3297-7.
Jie Pang, Yu-Bo Zhou, Li-Jun Liu, et al. Ring-closing-opening Copolymerization of Phthalaldehyde and Epoxide towards Acid-degradable Polyether and Polyurethane[J]. Chinese Journal of Polymer Science, 2025, 43(6): 964-972. DOI: 10.1007/s10118-025-3297-7.
Ring-closing-opening copolymerization of o-phthalaldehyde and epoxide occurs with organic Lewis pair catalysts
yielding polyacetals that are susceptible to acid degradation. Use of triethylborane reduces boronic ester formation
thus enhancing reaction control. Acetal-functionalized polyethers are produced when epoxide is used in large excess
and further transformed into acid-degradable polyurethane.
Incorporation of acetal groups in the backbone is a potent strategy to create polymers that are cleavable or degradable under acidic conditions. We report here an in-depth study on the ring-closing-opening copolymerization of
o
-phthalaldehyde (OPA) and epoxide using Lewis pair type two-component org
anocatalysts for producing acetal-functionalized polyether and polyurethane. Notably
triethylborane as the Lewis acid
in comparison with tri(
n
-butyl)borane
more effectively enhances the polymerization activity by mitigating borane-induced reduction of the aldehyde group into extra initiating (borinic ester) species. Density functional theory (DFT) calculations present comparable energy barriers of OPA-epoxide cross-propagation and epoxide self-propagation
which is consistent with the experimental finding that an alternating-rich copolymer comprising mostly OPA-epoxide units but also epoxide-epoxide linkages is produced. In particular
when epoxide is added in a large excess
the product becomes a polyether containing acetal functionalities in the central part of the backbone and thus being convertible into polyurethane with refined acid degradability.
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