Pd(ii) and Ni(ii) complexes featuring a “phosphasalen” ligand: synthesis and DFT study†

IF 3.5 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Dalton Transactions Pub Date : 2011-08-30 DOI:10.1039/C1DT10906E
Thi-Phuong-Anh Cao, Stéphanie Labouille, Audrey Auffrant, Yves Jean, Xavier F. Le Goff and Pascal Le Floch
{"title":"Pd(ii) and Ni(ii) complexes featuring a “phosphasalen” ligand: synthesis and DFT study†","authors":"Thi-Phuong-Anh Cao, Stéphanie Labouille, Audrey Auffrant, Yves Jean, Xavier F. Le Goff and Pascal Le Floch","doi":"10.1039/C1DT10906E","DOIUrl":null,"url":null,"abstract":"<p >A phosphorus analog of salen <annref>ligands</annref> featuring iminophosphorane functionalities in place of the imine groups was synthesised in 2 steps from <em>o</em>-diphenylphosphinophenol<em>via</em> the preparation of the corresponding bis-aminophosphonium salt. This novel tetradentate <annref>ligand</annref> (<strong>1</strong>), which we named phosphasalen, was coordinated to Pd(<small>II</small>) and Ni(<small>II</small>) metal centres affording complexes <strong>6</strong> and <strong>7</strong> respectively, which were characterised by multinuclear <annref>NMR</annref>, elemental and <annref>X-ray diffraction</annref> analyses. Both neutral complexes adopt a nearly square-planar geometry around the metal with coordination of all <compname>iminophosphorane</compname> and phenolate moieties. The electronic properties of these new complexes were investigated by <annref>cyclic voltammetry</annref> and comparison with known salens was made when possible. Moreover, the particular behaviour of the phosphasalen nickel complex <strong>7</strong> was further investigated through magnetic moment measurements and a DFT study.</p>","PeriodicalId":71,"journal":{"name":"Dalton Transactions","volume":" 39","pages":" 10029-10037"},"PeriodicalIF":3.5000,"publicationDate":"2011-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1039/C1DT10906E","citationCount":"19","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dalton Transactions","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2011/dt/c1dt10906e","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: 19

Abstract

A phosphorus analog of salen ligands featuring iminophosphorane functionalities in place of the imine groups was synthesised in 2 steps from o-diphenylphosphinophenolvia the preparation of the corresponding bis-aminophosphonium salt. This novel tetradentate ligand (1), which we named phosphasalen, was coordinated to Pd(II) and Ni(II) metal centres affording complexes 6 and 7 respectively, which were characterised by multinuclear NMR, elemental and X-ray diffraction analyses. Both neutral complexes adopt a nearly square-planar geometry around the metal with coordination of all iminophosphorane and phenolate moieties. The electronic properties of these new complexes were investigated by cyclic voltammetry and comparison with known salens was made when possible. Moreover, the particular behaviour of the phosphasalen nickel complex 7 was further investigated through magnetic moment measurements and a DFT study.

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
具有“磷酸体”配体的Pd(ii)和Ni(ii)配合物:合成和DFT研究†
以邻二苯基膦酚为原料,通过制备相应的双氨基膦盐,两步合成了一种具有亚胺磷烷官能团代替亚胺基的磷类似物。这种新型的四齿配体(1),我们将其命名为磷化体(phosphasalen),与Pd(II)和Ni(II)金属中心配位,分别形成配合物6和7,并通过多核磁共振、元素和x射线衍射分析对其进行了表征。这两种中性配合物在金属周围都采用接近方形平面的几何结构,并与所有亚磷和酚酸基团配位。用循环伏安法研究了这些新配合物的电子性质,并尽可能与已知的salens进行了比较。此外,通过磁矩测量和DFT研究进一步研究了磷酸体镍配合物7的特殊行为。
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
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.
期刊最新文献
The synergic effect of neutral organophosphorus ligands combined with acidic β-diketones for the extraction and separation of trivalent actinides Immobilization of palladium(II) acetate on a polymer-anchored Schiff base as a new heterogeneous catalyst for three-component one-Pot Mizoroki–Heck coupling via an in situ witting reaction How plutonium “brown” peroxo complex emerges from electrolysis experiments In situ Raman investigation of Dy complexation in Cl-bearing aqueous solutions at 20–300 °C Blue-light photodegradation of ferricyanide under protein relevant conditions †
×
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