{"title":"具有反应性P=P键的重氮二磷阳离子:合成和可逆主基团键激活","authors":"Jan Wieneke, Francesco Cirigliano, Marcel Schorpp","doi":"10.1039/d5cc04820f","DOIUrl":null,"url":null,"abstract":"We report a high-yielding synthesis of a novel diazadiphospholenium cation featuring a sterically exposed, reactive P=P bond. It displays aromatic properties and greater reactivity and selectivity than its parent diphosphene, enabling selective [4+2] cycloaddition and unusual, reversible E−E bond scission in diphenyldichalcogenides, highlighting its potential for main-group bond activation.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"114 1","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Diazadiphospholenium Cation Featuring a Reactive P=P Bond: Synthesis and Reversible Main-Group Bond Activation\",\"authors\":\"Jan Wieneke, Francesco Cirigliano, Marcel Schorpp\",\"doi\":\"10.1039/d5cc04820f\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We report a high-yielding synthesis of a novel diazadiphospholenium cation featuring a sterically exposed, reactive P=P bond. It displays aromatic properties and greater reactivity and selectivity than its parent diphosphene, enabling selective [4+2] cycloaddition and unusual, reversible E−E bond scission in diphenyldichalcogenides, highlighting its potential for main-group bond activation.\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"114 1\",\"pages\":\"\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-09-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5cc04820f\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5cc04820f","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
A Diazadiphospholenium Cation Featuring a Reactive P=P Bond: Synthesis and Reversible Main-Group Bond Activation
We report a high-yielding synthesis of a novel diazadiphospholenium cation featuring a sterically exposed, reactive P=P bond. It displays aromatic properties and greater reactivity and selectivity than its parent diphosphene, enabling selective [4+2] cycloaddition and unusual, reversible E−E bond scission in diphenyldichalcogenides, highlighting its potential for main-group bond activation.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.