Ruthenium, copper and ruthenium–copper complexes of an unsymmetrical phosphino pyridyl 1,8-naphthyridine PNNN ligand†

IF 3.5 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Jingyun Wu, Michael A. Stevens, Michael G. Gardiner and Annie L. Colebatch
{"title":"Ruthenium, copper and ruthenium–copper complexes of an unsymmetrical phosphino pyridyl 1,8-naphthyridine PNNN ligand†","authors":"Jingyun Wu, Michael A. Stevens, Michael G. Gardiner and Annie L. Colebatch","doi":"10.1039/D4DT02755H","DOIUrl":null,"url":null,"abstract":"<p >A new unsymmetrical dinucleating phosphino pyridyl 1,8-naphthyridine ligand PNNN is reported. Reaction with CuCl gave the dicopper complex [Cu<small><sub>2</sub></small>(μ-Cl)<small><sub>2</sub></small>(PNNN)] (<strong>1</strong>). In contrast, complexation of [RuCl<small><sub>2</sub></small>(cymene)]<small><sub>2</sub></small> yielded a monometallic species [RuCl(cymene)(PNNN)]Cl (<strong>[2]Cl</strong>) in which the Ru is bound to the κ<small><sup>2</sup></small>-N,N, rather than κ<small><sup>2</sup></small>-P,N, binding pocket. The selective formation of the monoruthenium complex <strong>[2]Cl</strong> enabled synthesis of heterobimetallic complexes [RuCuCl<small><sub>3</sub></small>(cymene)(PNNN)] (<strong>3</strong>) and [RuCuCl<small><sub>2</sub></small>(cymene)(PNNN)]<small><sub>2</sub></small>[PF<small><sub>6</sub></small>]<small><sub>2</sub></small> (<strong>[4]<small><sub>2</sub></small>[PF<small><sub>6</sub></small>]<small><sub>2</sub></small></strong>), which both exhibit κ<small><sup>1</sup></small>-P coordination of Cu. Complexes <strong>1</strong> and <strong>[4]<small><sub>2</sub></small>[PF<small><sub>6</sub></small>]<small><sub>2</sub></small></strong> exhibit reversible dearomatisation–aromatisation behaviour at the metal–ligand cooperative methylene site upon sequential treatment with base (KO<small><sup><em>t</em></sup></small>Bu) and acid (HCl). Notably, deprotonation of <strong>[4]<small><sub>2</sub></small>[PF<small><sub>6</sub></small>]<small><sub>2</sub></small></strong> induces a shift in the coordination mode of Cu to κ<small><sup>2</sup></small>-P,N.</p>","PeriodicalId":71,"journal":{"name":"Dalton Transactions","volume":" 44","pages":" 18037-18046"},"PeriodicalIF":3.5000,"publicationDate":"2024-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dalton Transactions","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/dt/d4dt02755h","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

A new unsymmetrical dinucleating phosphino pyridyl 1,8-naphthyridine ligand PNNN is reported. Reaction with CuCl gave the dicopper complex [Cu2(μ-Cl)2(PNNN)] (1). In contrast, complexation of [RuCl2(cymene)]2 yielded a monometallic species [RuCl(cymene)(PNNN)]Cl ([2]Cl) in which the Ru is bound to the κ2-N,N, rather than κ2-P,N, binding pocket. The selective formation of the monoruthenium complex [2]Cl enabled synthesis of heterobimetallic complexes [RuCuCl3(cymene)(PNNN)] (3) and [RuCuCl2(cymene)(PNNN)]2[PF6]2 ([4]2[PF6]2), which both exhibit κ1-P coordination of Cu. Complexes 1 and [4]2[PF6]2 exhibit reversible dearomatisation–aromatisation behaviour at the metal–ligand cooperative methylene site upon sequential treatment with base (KOtBu) and acid (HCl). Notably, deprotonation of [4]2[PF6]2 induces a shift in the coordination mode of Cu to κ2-P,N.

Abstract Image

非对称膦吡啶-1,8-萘啶 PNNN 配体的钌、铜和钌铜配合物
报告了一种新的非对称二核膦基吡啶-1,8-萘啶配体 PNNN。与 CuCl 反应生成了二铜络合物 [Cu2(µ-Cl)2(PNN)](1)。与此相反,[RuCl2(cymene)]2 的络合产生了单金属物种 [RuCl(cymene)(PNNN)]Cl([2]Cl),其中的 Ru 与 κ2-N,N 结合,而不是与 κ2-P,N 结合。单钌络合物 [2]Cl 的选择性形成使得[RuCuCl3(cymene)(PNNN)](3)和[RuCuCl2(cymene)(PNNN)]2[PF6]2([4]2[PF6]2)这两种杂多金属络合物得以合成,它们都表现出 Cu 的κ1-P 配位。配合物 1 和 [4]2[PF6]2 依次经碱(KOtBu)和酸(HCl)处理后,在金属配体合作亚甲基位点上表现出可逆的脱芳基化-芳基化行为。值得注意的是,[4]2[PF6]2 的去质子化会导致铜的配位模式转变为 κ2-P,N。
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
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
×
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