Study on the cleavage of alkyl-O-aryl bonds by in situ generated hydroxyl radicals on an ORR cathode. Issue 81 (6th November 2017)

• Record Type: Journal Article
• Authors: Wang, Lei; Chen, Yongmei; Liu, Shuangyan; Jiang, Haomin; Wang, Linan; Sun, Yanzhi; Wan, Pingyu
• Is Part Of: RSC advances. Volume 7:Issue 81(2017)
• Page Start: 51419
• Page End: 51425
• Publication Date: 2017-11-06
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c7ra11236j
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : ˙OH selectively attacks the active sites opposite to phenolic hydroxyl groups and leads to bond-cleavage of ether bonds. Abstract : Hydroxyl radicals (˙OH) generated by oxygen reduction reaction (ORR) were believed to be responsible for the electrochemical depolymerization of lignin in our previous study. However, the mechanism research was hard to carry out due to the recalcitrant nature of lignin. In this paper, 4-benzyloxyl phenol (PBP) and benzyl phenyl ether (BPE) were employed as lignin model compounds (LMCs). Based on the qualitative and quantitative analysis of the degradation products, a mechanism was put forward, which is that the in situ generated ˙OH selectively attacked the active site opposite to the phenolic hydroxyl group and induced the cleavage of the alkyl- O -aryl ether bond. The proposed mechanism was further verified by the electrochemical degradation of PBP under controlled conditions, which showed a positive correlation between the degradation efficiency of PBP and the concentration of in situ generated ˙OH radicals.