Chunming Cui, Marilyn M. Olmstead, Philip P. Power
{"title":"Ar ' gegear ' (Ar ' = C6H3-2,6-Dipp2, Dipp = C6H3-2,6-iPr2)对炔烃的反应性:稳定二聚环丁二烯的分离","authors":"Chunming Cui, Marilyn M. Olmstead, Philip P. Power","doi":"10.1021/ja0318481","DOIUrl":null,"url":null,"abstract":"<p >The first reactions of the “digermyne” Ar‘GeGeAr‘ (<b>1</b>, Ar‘ = C<sub>6</sub>H<sub>3</sub>-2,6-Dipp<sub>2</sub>, Dipp = C<sub>6</sub>H<sub>3</sub>-2,6-<i>i</i>Pr<sub>2</sub>) with alkynes are reported. <b>1</b> reacts with 1 equiv of H<sub>5</sub>C<sub>6</sub>CCC<sub>6</sub>H<sub>5</sub> to afford the 1,2-digermacyclobutadiene <b>2</b> in high yield, while it reacts with 2 equiv of the less hindered alkyne Me<sub>3</sub>SiCCH to yield an unexpected bicyclic compound <b>3</b>. Molecular structures of <b>2</b> and <b>3</b> were determined by X-ray crystallography. A possible mechanism for the formation of <b>3</b> is discussed. The high reactivity of <b>1</b>, even at room temperature, emphasizes the fundamental differences between the GeGe and CC multiple bonds. </p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"126 16","pages":"5062–5063"},"PeriodicalIF":15.6000,"publicationDate":"2004-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1021/ja0318481","citationCount":"82","resultStr":"{\"title\":\"Reactivity of Ar‘GeGeAr‘ (Ar‘ = C6H3-2,6-Dipp2, Dipp = C6H3-2,6-iPr2) toward Alkynes: Isolation of a Stable Digermacyclobutadiene\",\"authors\":\"Chunming Cui, Marilyn M. Olmstead, Philip P. Power\",\"doi\":\"10.1021/ja0318481\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The first reactions of the “digermyne” Ar‘GeGeAr‘ (<b>1</b>, Ar‘ = C<sub>6</sub>H<sub>3</sub>-2,6-Dipp<sub>2</sub>, Dipp = C<sub>6</sub>H<sub>3</sub>-2,6-<i>i</i>Pr<sub>2</sub>) with alkynes are reported. <b>1</b> reacts with 1 equiv of H<sub>5</sub>C<sub>6</sub>CCC<sub>6</sub>H<sub>5</sub> to afford the 1,2-digermacyclobutadiene <b>2</b> in high yield, while it reacts with 2 equiv of the less hindered alkyne Me<sub>3</sub>SiCCH to yield an unexpected bicyclic compound <b>3</b>. Molecular structures of <b>2</b> and <b>3</b> were determined by X-ray crystallography. A possible mechanism for the formation of <b>3</b> is discussed. The high reactivity of <b>1</b>, even at room temperature, emphasizes the fundamental differences between the GeGe and CC multiple bonds. </p>\",\"PeriodicalId\":49,\"journal\":{\"name\":\"Journal of the American Chemical Society\",\"volume\":\"126 16\",\"pages\":\"5062–5063\"},\"PeriodicalIF\":15.6000,\"publicationDate\":\"2004-03-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1021/ja0318481\",\"citationCount\":\"82\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the American Chemical Society\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/ja0318481\",\"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/ja0318481","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Reactivity of Ar‘GeGeAr‘ (Ar‘ = C6H3-2,6-Dipp2, Dipp = C6H3-2,6-iPr2) toward Alkynes: Isolation of a Stable Digermacyclobutadiene
The first reactions of the “digermyne” Ar‘GeGeAr‘ (1, Ar‘ = C6H3-2,6-Dipp2, Dipp = C6H3-2,6-iPr2) with alkynes are reported. 1 reacts with 1 equiv of H5C6CCC6H5 to afford the 1,2-digermacyclobutadiene 2 in high yield, while it reacts with 2 equiv of the less hindered alkyne Me3SiCCH to yield an unexpected bicyclic compound 3. Molecular structures of 2 and 3 were determined by X-ray crystallography. A possible mechanism for the formation of 3 is discussed. The high reactivity of 1, even at room temperature, emphasizes the fundamental differences between the GeGe and CC multiple bonds.
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.