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

IF 15.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
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,&nbsp;Marilyn M. Olmstead,&nbsp;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,&nbsp;Marilyn M. Olmstead,&nbsp;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}
引用次数: 82

摘要

报道了“双双胺”Ar ' gegear (1, Ar ' = C6H3-2,6-Dipp2, Dipp = C6H3-2,6-iPr2)与炔烃的首次反应。1与1等量的H5C6CCC6H5反应生成高产的1,2-二聚环丁二烯2,而与2等量的阻碍较小的炔Me3SiCCH反应生成意想不到的双环化合物3。用x射线晶体学测定了2和3的分子结构。讨论了3的可能形成机理。即使在室温下,1的高反应性也强调了GeGe和CC多键之间的根本区别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Reactivity of Ar‘GeGeAr‘ (Ar‘ = C6H3-2,6-Dipp2, Dipp = C6H3-2,6-iPr2) toward Alkynes:  Isolation of a Stable Digermacyclobutadiene

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信