{"title":"锗介导的Ge(II)/Ge(III)/Ge(IV)或Ge(II)/Ge(IV)氧化还原循环催化","authors":"Yihan Zhou, , , Zhuchunguang Liu, , , Huan Mu, , , Hanjiao Chen, , , Xinran Fu, , , Bo Xiao, , , Weichao Xue, , , Jiliang Zhou, , and , Zhaowen Dong*, ","doi":"10.1021/jacs.5c12407","DOIUrl":null,"url":null,"abstract":"<p >Main group elements have recently emerged as promising candidates for redox catalysis, challenging the traditional reliance on transition metals. Despite heavy group 14 elements, such as germanium, possessing variable oxidation states that suggest their redox catalytic potential, their practical applications have been limited. In this study, we present the synthesis of a carbodiphosphoranyl germanium(II) compound and investigate its redox catalytic application. This organogermanium(II) species exhibits excellent catalytic performance in promoting the transfer hydrogenation of azoarenes and imines under mild conditions. Mechanistic studies revealed two distinct catalytic platforms based on Ge<sup>II</sup>/Ge<sup>III</sup>/Ge<sup>IV</sup> and Ge<sup>II</sup>/Ge<sup>IV</sup> redox cycles at a single germanium center. These results enable us to achieve the catalytic hydrogenation of azoarenes mediated by frustrated radical pairs (FRPs), as well as the catalytic chemoselective dearomatization of <i>N</i>-heteroarenes undergoing a Ge<sup>II</sup>/Ge<sup>IV</sup> redox process. Our work demonstrates the capacity of main group catalysts to facilitate diverse challenging chemical transformations through regulating the catalytic modes.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"147 40","pages":"36752–36762"},"PeriodicalIF":15.6000,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Germanium-Mediated Catalysis via Ge(II)/Ge(III)/Ge(IV) or Ge(II)/Ge(IV) Redox Cycling\",\"authors\":\"Yihan Zhou, , , Zhuchunguang Liu, , , Huan Mu, , , Hanjiao Chen, , , Xinran Fu, , , Bo Xiao, , , Weichao Xue, , , Jiliang Zhou, , and , Zhaowen Dong*, \",\"doi\":\"10.1021/jacs.5c12407\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Main group elements have recently emerged as promising candidates for redox catalysis, challenging the traditional reliance on transition metals. Despite heavy group 14 elements, such as germanium, possessing variable oxidation states that suggest their redox catalytic potential, their practical applications have been limited. In this study, we present the synthesis of a carbodiphosphoranyl germanium(II) compound and investigate its redox catalytic application. This organogermanium(II) species exhibits excellent catalytic performance in promoting the transfer hydrogenation of azoarenes and imines under mild conditions. Mechanistic studies revealed two distinct catalytic platforms based on Ge<sup>II</sup>/Ge<sup>III</sup>/Ge<sup>IV</sup> and Ge<sup>II</sup>/Ge<sup>IV</sup> redox cycles at a single germanium center. These results enable us to achieve the catalytic hydrogenation of azoarenes mediated by frustrated radical pairs (FRPs), as well as the catalytic chemoselective dearomatization of <i>N</i>-heteroarenes undergoing a Ge<sup>II</sup>/Ge<sup>IV</sup> redox process. Our work demonstrates the capacity of main group catalysts to facilitate diverse challenging chemical transformations through regulating the catalytic modes.</p>\",\"PeriodicalId\":49,\"journal\":{\"name\":\"Journal of the American Chemical Society\",\"volume\":\"147 40\",\"pages\":\"36752–36762\"},\"PeriodicalIF\":15.6000,\"publicationDate\":\"2025-09-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/jacs.5c12407\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/jacs.5c12407","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Germanium-Mediated Catalysis via Ge(II)/Ge(III)/Ge(IV) or Ge(II)/Ge(IV) Redox Cycling
Main group elements have recently emerged as promising candidates for redox catalysis, challenging the traditional reliance on transition metals. Despite heavy group 14 elements, such as germanium, possessing variable oxidation states that suggest their redox catalytic potential, their practical applications have been limited. In this study, we present the synthesis of a carbodiphosphoranyl germanium(II) compound and investigate its redox catalytic application. This organogermanium(II) species exhibits excellent catalytic performance in promoting the transfer hydrogenation of azoarenes and imines under mild conditions. Mechanistic studies revealed two distinct catalytic platforms based on GeII/GeIII/GeIV and GeII/GeIV redox cycles at a single germanium center. These results enable us to achieve the catalytic hydrogenation of azoarenes mediated by frustrated radical pairs (FRPs), as well as the catalytic chemoselective dearomatization of N-heteroarenes undergoing a GeII/GeIV redox process. Our work demonstrates the capacity of main group catalysts to facilitate diverse challenging chemical transformations through regulating the catalytic modes.
期刊介绍:
The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.