{"title":"非芳香族化合物催化脱氢芳构化合成偶氮苯","authors":"Wei-Chen Lin, Takafumi Yatabe*, Heizo Kimura, Tomohiro Yabe and Kazuya Yamaguchi*, ","doi":"10.1021/acscatal.5c0180710.1021/acscatal.5c01807","DOIUrl":null,"url":null,"abstract":"<p >Azobenzenes have been ubiquitously utilized and synthesized in well-established methods represented as azo coupling for a long time; however, all the available azobenzene synthesis strategies use aromatic compounds as substrates, which inherently limit the regioselectivity of substituents because of <i>ortho</i>/<i>meta</i>/<i>para</i>-orientation and frequently require multistep procedures. Dehydrogenative aromatization from cyclohexanones, which can be regioselectively functionalized using classical methods without the aforementioned limitation, has recently attracted attention, but the lack of multifunctional dehydrogenation catalysts for both aromatization and azo bond formation and/or the difficult product selectivity control have hindered its application in azobenzene synthesis. Herein, we report an unprecedented strategy for the synthesis of diverse azobenzenes, including unsymmetrical ones, from only nonaromatic compounds, that is, cyclohexanones and hydrazine, using an Au–Pd alloy nanoparticle catalyst and a suitable hydrogen acceptor (nitrobenzene). Thorough mechanistic studies revealed that the present reaction is enabled by adsorption control and relay catalysis involving concerted dehydrogenation, which are unique features of alloy nanoparticles.</p>","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"15 12","pages":"10651–10662 10651–10662"},"PeriodicalIF":13.1000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Azobenzene Synthesis from Only Nonaromatic Compounds via Catalytic Dehydrogenative Aromatization\",\"authors\":\"Wei-Chen Lin, Takafumi Yatabe*, Heizo Kimura, Tomohiro Yabe and Kazuya Yamaguchi*, \",\"doi\":\"10.1021/acscatal.5c0180710.1021/acscatal.5c01807\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Azobenzenes have been ubiquitously utilized and synthesized in well-established methods represented as azo coupling for a long time; however, all the available azobenzene synthesis strategies use aromatic compounds as substrates, which inherently limit the regioselectivity of substituents because of <i>ortho</i>/<i>meta</i>/<i>para</i>-orientation and frequently require multistep procedures. Dehydrogenative aromatization from cyclohexanones, which can be regioselectively functionalized using classical methods without the aforementioned limitation, has recently attracted attention, but the lack of multifunctional dehydrogenation catalysts for both aromatization and azo bond formation and/or the difficult product selectivity control have hindered its application in azobenzene synthesis. Herein, we report an unprecedented strategy for the synthesis of diverse azobenzenes, including unsymmetrical ones, from only nonaromatic compounds, that is, cyclohexanones and hydrazine, using an Au–Pd alloy nanoparticle catalyst and a suitable hydrogen acceptor (nitrobenzene). Thorough mechanistic studies revealed that the present reaction is enabled by adsorption control and relay catalysis involving concerted dehydrogenation, which are unique features of alloy nanoparticles.</p>\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":\"15 12\",\"pages\":\"10651–10662 10651–10662\"},\"PeriodicalIF\":13.1000,\"publicationDate\":\"2025-06-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acscatal.5c01807\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acscatal.5c01807","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Azobenzene Synthesis from Only Nonaromatic Compounds via Catalytic Dehydrogenative Aromatization
Azobenzenes have been ubiquitously utilized and synthesized in well-established methods represented as azo coupling for a long time; however, all the available azobenzene synthesis strategies use aromatic compounds as substrates, which inherently limit the regioselectivity of substituents because of ortho/meta/para-orientation and frequently require multistep procedures. Dehydrogenative aromatization from cyclohexanones, which can be regioselectively functionalized using classical methods without the aforementioned limitation, has recently attracted attention, but the lack of multifunctional dehydrogenation catalysts for both aromatization and azo bond formation and/or the difficult product selectivity control have hindered its application in azobenzene synthesis. Herein, we report an unprecedented strategy for the synthesis of diverse azobenzenes, including unsymmetrical ones, from only nonaromatic compounds, that is, cyclohexanones and hydrazine, using an Au–Pd alloy nanoparticle catalyst and a suitable hydrogen acceptor (nitrobenzene). Thorough mechanistic studies revealed that the present reaction is enabled by adsorption control and relay catalysis involving concerted dehydrogenation, which are unique features of alloy nanoparticles.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.