Synthesis and Reactivity of Iron and Cobalt Bis(amidophosphine selenide) Complexes

IF 2.5 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Daniel Y. Zhou, Kelsey S. Zimmerman, Paige M. Gannon, Sebastian M. Krajewski, Werner Kaminsky, Benjamin S. Mitchell* and Alexandra Velian*, 
{"title":"Synthesis and Reactivity of Iron and Cobalt Bis(amidophosphine selenide) Complexes","authors":"Daniel Y. Zhou,&nbsp;Kelsey S. Zimmerman,&nbsp;Paige M. Gannon,&nbsp;Sebastian M. Krajewski,&nbsp;Werner Kaminsky,&nbsp;Benjamin S. Mitchell* and Alexandra Velian*,&nbsp;","doi":"10.1021/acs.organomet.4c0046810.1021/acs.organomet.4c00468","DOIUrl":null,"url":null,"abstract":"<p >We report the synthesis of two metal bis(amidophosphine selenide) complexes, ML<sub>2</sub> (M = Fe, Co; L = SePPh<sub>2</sub>N<sup>(−)</sup>Tol), and investigate their reactivity toward ligand binding and oxidation with oxygen atom transfer reagents, pyridine-<i>N</i>-oxide and mesityl nitrile oxide. The oxidative strength of the reagent dictates the nature of the reactivity: either the ligand is oxidized, leading to the formation of a bimetallic mixed-ligand complex [MLL′]<sub><i>n</i></sub>, (L′ = OPPh<sub>2</sub>N<sup>(−)</sup>Tol), or the metal center is oxidized, resulting in a bimetallic μ-oxo complex [FeL<sub>2</sub>]<sub>2</sub>(μ<sub>2</sub>-O). This study defines a chemical space in which amidophosphine selenide ligands maintain their structural integrity.</p>","PeriodicalId":56,"journal":{"name":"Organometallics","volume":"44 1","pages":"335–339 335–339"},"PeriodicalIF":2.5000,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organometallics","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.organomet.4c00468","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

Abstract

We report the synthesis of two metal bis(amidophosphine selenide) complexes, ML2 (M = Fe, Co; L = SePPh2N(−)Tol), and investigate their reactivity toward ligand binding and oxidation with oxygen atom transfer reagents, pyridine-N-oxide and mesityl nitrile oxide. The oxidative strength of the reagent dictates the nature of the reactivity: either the ligand is oxidized, leading to the formation of a bimetallic mixed-ligand complex [MLL′]n, (L′ = OPPh2N(−)Tol), or the metal center is oxidized, resulting in a bimetallic μ-oxo complex [FeL2]22-O). This study defines a chemical space in which amidophosphine selenide ligands maintain their structural integrity.

Abstract Image

铁钴双(氨基膦硒化)配合物的合成及反应性
本文报道了两种金属双(氨基膦硒化物)配合物的合成,ML2 (M = Fe, Co;L = SePPh2N(−)Tol),并研究了它们与氧原子转移试剂吡啶- n -氧化物和甲腈氧化物结合和氧化的反应性。试剂的氧化强度决定了反应性的性质:要么配体被氧化,形成双金属混合配体配合物[MLL ']n, (L ' = OPPh2N(−)Tol),要么金属中心被氧化,形成双金属μ-氧配合物[FeL2]2(μ2-O)。本研究定义了一个化学空间,其中氨基膦硒化物配体保持其结构完整性。
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 求助全文
来源期刊
Organometallics
Organometallics 化学-无机化学与核化学
CiteScore
5.60
自引率
7.10%
发文量
382
审稿时长
1.7 months
期刊介绍: Organometallics is the flagship journal of organometallic chemistry and records progress in one of the most active fields of science, bridging organic and inorganic chemistry. The journal publishes Articles, Communications, Reviews, and Tutorials (instructional overviews) that depict research on the synthesis, structure, bonding, chemical reactivity, and reaction mechanisms for a variety of applications, including catalyst design and catalytic processes; main-group, transition-metal, and lanthanide and actinide metal chemistry; synthetic aspects of polymer science and materials science; and bioorganometallic chemistry.
×
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:481959085
Book学术官方微信