钯阴离子配合物催化芳基硅烷高效功能化烯烃

IF 5.062

Journal of Molecular Catalysis A: Chemical Pub Date : 2017-01-01 DOI:10.1016/j.molcata.2016.07.023

E. Silarska , M. Majchrzak , B. Marciniec , A.M. Trzeciak

{"title":"钯阴离子配合物催化芳基硅烷高效功能化烯烃","authors":"E. Silarska , M. Majchrzak , B. Marciniec , A.M. Trzeciak","doi":"10.1016/j.molcata.2016.07.023","DOIUrl":null,"url":null,"abstract":"<div>The coupling of organosilanes and different olefins was performed efficiently in the presence of anionic complexes, [CA]2[PdX4] and [CA]2[Pd2X6], where CA=imidazolium or pyridinium cation. The reaction proceeds according to a Pd(II)-mediated pathway, and Cu(OAc)2 acts as the re-oxidant of Pd(0) formed during the catalytic process. High product yields were obtained for differently substituted olefins at 80°C in 4h. Styrylsilanes reacted in the same conditions giving unsymmetrical 1,3-dienes.</div>","PeriodicalId":370,"journal":{"name":"Journal of Molecular Catalysis A: Chemical","volume":"426 ","pages":"Pages 458-464"},"PeriodicalIF":5.0620,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.molcata.2016.07.023","citationCount":"6","resultStr":"{\"title\":\"Efficient functionalization of olefins by arylsilanes catalyzed by palladium anionic complexes\",\"authors\":\"E. Silarska , M. Majchrzak , B. Marciniec , A.M. Trzeciak\",\"doi\":\"10.1016/j.molcata.2016.07.023\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>The coupling of organosilanes and different olefins was performed efficiently in the presence of anionic complexes, [CA]2[PdX4] and [CA]2[Pd2X6], where CA=imidazolium or pyridinium cation. The reaction proceeds according to a Pd(II)-mediated pathway, and Cu(OAc)2 acts as the re-oxidant of Pd(0) formed during the catalytic process. High product yields were obtained for differently substituted olefins at 80°C in 4h. Styrylsilanes reacted in the same conditions giving unsymmetrical 1,3-dienes.</div>\",\"PeriodicalId\":370,\"journal\":{\"name\":\"Journal of Molecular Catalysis A: Chemical\",\"volume\":\"426 \",\"pages\":\"Pages 458-464\"},\"PeriodicalIF\":5.0620,\"publicationDate\":\"2017-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.molcata.2016.07.023\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Molecular Catalysis A: Chemical\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1381116916302734\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Catalysis A: Chemical","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1381116916302734","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}

引用次数: 6

摘要

在阴离子配合物[CA]2[PdX4]和[CA]2[Pd2X6]的存在下，有机硅烷与不同的烯烃进行了有效的偶联，其中CA =咪唑或吡啶阳离子。反应根据Pd(II)介导的途径进行，Cu(OAc)2作为催化过程中生成的Pd(0)的再氧化剂。不同取代的烯烃在80℃下反应4 h得到了较高的产率。苯乙烯基硅烷在相同条件下反应得到不对称的1,3-二烯。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Efficient functionalization of olefins by arylsilanes catalyzed by palladium anionic complexes

查看原文本刊更多论文

Efficient functionalization of olefins by arylsilanes catalyzed by palladium anionic complexes

The coupling of organosilanes and different olefins was performed efficiently in the presence of anionic complexes, [CA]₂[PdX₄] and [CA]₂[Pd₂X₆], where CA = imidazolium or pyridinium cation. The reaction proceeds according to a Pd(II)-mediated pathway, and Cu(OAc)₂ acts as the re-oxidant of Pd(0) formed during the catalytic process. High product yields were obtained for differently substituted olefins at 80 °C in 4 h. Styrylsilanes reacted in the same conditions giving unsymmetrical 1,3-dienes.

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

Journal of Molecular Catalysis A: Chemical 化学-物理化学

自引率

0.00%

发文量

审稿时长

2.8 months

期刊介绍： The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.