Palladium Bisphosphine Monoxide Complexes: Synthesis, Scope, Mechanism, and Catalytic Relevance

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2024-12-17 DOI:10.1021/jacs.4c10718
Shenghua Yang, Min Deng, Ryan A. Daley, Andrea Darù, William J. Wolf, David T. George, Senjie Ma, Bryn K. Werley, Erika Samolova, Jake B. Bailey, Milan Gembicky, Jonathan Marshall, Steven R. Wisniewski, Donna G. Blackmond, Keary M. Engle
{"title":"Palladium Bisphosphine Monoxide Complexes: Synthesis, Scope, Mechanism, and Catalytic Relevance","authors":"Shenghua Yang, Min Deng, Ryan A. Daley, Andrea Darù, William J. Wolf, David T. George, Senjie Ma, Bryn K. Werley, Erika Samolova, Jake B. Bailey, Milan Gembicky, Jonathan Marshall, Steven R. Wisniewski, Donna G. Blackmond, Keary M. Engle","doi":"10.1021/jacs.4c10718","DOIUrl":null,"url":null,"abstract":"Recent studies in transition metal catalysis employing chelating phosphines have suggested a role for partial ligand oxidation in formation of the catalytically active species, with potentially widespread relevance in a number of catalytic systems. We examine the internal redox reaction of Pd<sup>II</sup>(bisphosphine)X<sub>2</sub> (X = Cl, OAc, <i>etc.</i>) complexes to reveal previously underexplored aspects of bisphosphine monoxides (BPMOs), including evaluation of ligand structure and development of general reaction conditions to access a collection of structurally diverse BPMO precatalysts based on organopalladium oxidative addition complexes. In particular, a series of Pd<sup>II</sup>(BPMO)(R)(X) (R = aryl, alkyl; X = I, Br) oxidative addition complexes bearing 24 different BPMO ligands were characterized by NMR and X-ray crystallography. Comparison of the catalytic performance of the oxidative addition complexes of bisphosphine versus bisphosphine monoxides as precatalysts is demonstrated to be an enabling diagnostic tool in Pd catalytic reaction development. Finally, the differences in catalytic behavior between bisphosphine and bisphosphine monoxide complexes were rationalized through solid-state parametrization and stoichiometric experiments.","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"87 1","pages":""},"PeriodicalIF":14.4000,"publicationDate":"2024-12-17","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://doi.org/10.1021/jacs.4c10718","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: 0

Abstract

Recent studies in transition metal catalysis employing chelating phosphines have suggested a role for partial ligand oxidation in formation of the catalytically active species, with potentially widespread relevance in a number of catalytic systems. We examine the internal redox reaction of PdII(bisphosphine)X2 (X = Cl, OAc, etc.) complexes to reveal previously underexplored aspects of bisphosphine monoxides (BPMOs), including evaluation of ligand structure and development of general reaction conditions to access a collection of structurally diverse BPMO precatalysts based on organopalladium oxidative addition complexes. In particular, a series of PdII(BPMO)(R)(X) (R = aryl, alkyl; X = I, Br) oxidative addition complexes bearing 24 different BPMO ligands were characterized by NMR and X-ray crystallography. Comparison of the catalytic performance of the oxidative addition complexes of bisphosphine versus bisphosphine monoxides as precatalysts is demonstrated to be an enabling diagnostic tool in Pd catalytic reaction development. Finally, the differences in catalytic behavior between bisphosphine and bisphosphine monoxide complexes were rationalized through solid-state parametrization and stoichiometric experiments.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
最近对使用螯合膦的过渡金属催化作用的研究表明,部分配体氧化在催化活性物质的形成过程中起着重要作用,这在许多催化体系中都具有潜在的广泛意义。我们研究了 PdII(双膦)X2(X = Cl、OAc 等)配合物的内部氧化还原反应,以揭示双膦单氧化物(BPMOs)以前未充分探索的方面,包括评估配体结构和开发一般反应条件,以获得一系列基于有机钯氧化加成配合物的结构多样的 BPMO 前催化剂。其中,一系列带有 24 种不同 BPMO 配体的 PdII(BPMO)(R)(X)(R = 芳基、烷基;X = I、Br)氧化加成配合物通过核磁共振和 X 射线晶体学进行了表征。比较了作为前催化剂的双膦氧化加成络合物与双膦一氧化物的催化性能,结果表明,这是在钯催化反应开发过程中的一种有效诊断工具。最后,通过固态参数化和化学计量实验合理解释了双膦和双膦一氧化物配合物在催化行为上的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 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.
期刊最新文献
Palladium Bisphosphine Monoxide Complexes: Synthesis, Scope, Mechanism, and Catalytic Relevance Stable Na/K–S Batteries with Conductive Organosulfur Polymer Microcages as Cathodes Iridium-Catalyzed Enantioconvergent Construction of Piperidines and Tetrahydroisoquinolines from Racemic 1,5-Diols Formation and Reactivity of a MnIV(O)(μ-O)CeIV Species: A Closest Mimic of Photosystem II Total Synthesis of (+)-Mannolide B
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1