“…The proton signals from N-H (δ = 4.67 ppm) and -CH 3 (δ = 3.66 ppm) proved the formation of methyl butyl carbamate (MBC) (Fig.9c), which was in agreement with the degradation experiments of RE-PHUs. Based on the experiments and previous reports,38 the degradation of RE-PHUs may undergo the following mechanism: the attack of Na + on the CvO in carbamate protonated it, resulting in CvO being more susceptible to nucleophilic attack by methanol; meanwhile, OH − slightly deviated the hydrogen atoms in methanol, making oxygen atoms in methanol more negatively charged and easier to attack carbon atoms in CvO. As shown in Scheme S3, † the degradation process mainly included the activation of carbonyls, nucleophilic attack of methoxy, and elimination of leaving groups.…”