Zhe Wang, Yimei Chen, Zhouyang Long, Yunfei Wang, Mingming Fan, Pingbo Zhang and Yan Leng
{"title":"Mo2C-derived molybdenum oxycarbides afford controllable oxidation of anilines to azobenzenes and azoxybenzenes†","authors":"Zhe Wang, Yimei Chen, Zhouyang Long, Yunfei Wang, Mingming Fan, Pingbo Zhang and Yan Leng","doi":"10.1039/D4GC06281G","DOIUrl":null,"url":null,"abstract":"<p >The catalytic synthesis of aromatic azo compounds <em>via</em> oxidative coupling of anilines still faces great challenges due to the difficulty in controlling product selectivity. In this study, we have pioneered the application of Mo<small><sub>2</sub></small>C as a pre-catalyst for the selective oxidation of aniline using H<small><sub>2</sub></small>O<small><sub>2</sub></small> to produce azobenzenes and azoxybenzenes. Both experimental and theoretical studies reveal that H<small><sub>2</sub></small>O<small><sub>2</sub></small> induces the formation of Mo oxycarbides (MoC<small><sub><em>x</em></sub></small>O<small><sub><em>y</em></sub></small>) on the surface of Mo<small><sub>2</sub></small>C during the reaction, which subsequently activates H<small><sub>2</sub></small>O<small><sub>2</sub></small> to generate active sites (Mo⋯O) essential for the oxidative coupling of anilines. Furthermore, the kinetics of the critical conversion from Ph-NH<small><sub>2</sub></small> to Ph-NHOH over MoC<small><sub><em>x</em></sub></small>O<small><sub><em>y</em></sub></small> can be adjusted by modulating the solvent, thereby enabling controlled product selectivity between azobenzenes and azoxybenzenes. This work elucidates the structural evolution of Mo<small><sub>2</sub></small>C to MoC<small><sub><em>x</em></sub></small>O<small><sub><em>y</em></sub></small> in a H<small><sub>2</sub></small>O<small><sub>2</sub></small> system and its catalytic oxidation capabilities, potentially paving the way for broader applications of MoC<small><sub><em>x</em></sub></small>O<small><sub><em>y</em></sub></small> in various oxidation reactions.</p>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":" 11","pages":" 3091-3098"},"PeriodicalIF":9.3000,"publicationDate":"2025-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/gc/d4gc06281g","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The catalytic synthesis of aromatic azo compounds via oxidative coupling of anilines still faces great challenges due to the difficulty in controlling product selectivity. In this study, we have pioneered the application of Mo2C as a pre-catalyst for the selective oxidation of aniline using H2O2 to produce azobenzenes and azoxybenzenes. Both experimental and theoretical studies reveal that H2O2 induces the formation of Mo oxycarbides (MoCxOy) on the surface of Mo2C during the reaction, which subsequently activates H2O2 to generate active sites (Mo⋯O) essential for the oxidative coupling of anilines. Furthermore, the kinetics of the critical conversion from Ph-NH2 to Ph-NHOH over MoCxOy can be adjusted by modulating the solvent, thereby enabling controlled product selectivity between azobenzenes and azoxybenzenes. This work elucidates the structural evolution of Mo2C to MoCxOy in a H2O2 system and its catalytic oxidation capabilities, potentially paving the way for broader applications of MoCxOy in various oxidation reactions.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.