Guest selectivity of [Ni2] supramolecular helicates†

IF 3.3 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Dalton Transactions Pub Date : 2024-06-29 DOI:10.1039/D4DT01611D
Manuel Imperato, Alessio Nicolini, Jordi Ribas-Ariño, Michał Antkowiak, Olivier Roubeau, Andrea Cornia, Valentin Novikov, Leoní A. Barrios and Guillem Aromí
{"title":"Guest selectivity of [Ni2] supramolecular helicates†","authors":"Manuel Imperato, Alessio Nicolini, Jordi Ribas-Ariño, Michał Antkowiak, Olivier Roubeau, Andrea Cornia, Valentin Novikov, Leoní A. Barrios and Guillem Aromí","doi":"10.1039/D4DT01611D","DOIUrl":null,"url":null,"abstract":"<p >Two new paramagnetic supramolecular helicates with the formula (X@[Ni<small><sub>2</sub></small><strong>L</strong><small><sub>3</sub></small>])<small><sup>3+</sup></small> (X = Cl, or Br; <strong>L</strong> = a bis-pyrazolylpyridine ligand) have been prepared and are described. Helicates of this metal are very rare with virtually no prior examples of them acting as hosts of anionic species. The persistence of the new assemblies in solution has been demonstrated unambiguously by mass spectrometry and paramagnetic <small><sup>1</sup></small>H NMR. This has allowed us to establish the preference of the coordination [Ni<small><sub>2</sub></small>] host for Cl<small><sup>−</sup></small> over Br<small><sup>−</sup></small>, in agreement with DFT calculations. These results show the promise of the use of metallohelicates as suitable systems for the selective encapsulation of specific anions in solution.</p>","PeriodicalId":71,"journal":{"name":"Dalton Transactions","volume":" 29","pages":" 12301-12306"},"PeriodicalIF":3.3000,"publicationDate":"2024-06-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/dt/d4dt01611d?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dalton Transactions","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/dt/d4dt01611d","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

Two new paramagnetic supramolecular helicates with the formula (X@[Ni2L3])3+ (X = Cl, or Br; L = a bis-pyrazolylpyridine ligand) have been prepared and are described. Helicates of this metal are very rare with virtually no prior examples of them acting as hosts of anionic species. The persistence of the new assemblies in solution has been demonstrated unambiguously by mass spectrometry and paramagnetic 1H NMR. This has allowed us to establish the preference of the coordination [Ni2] host for Cl over Br, in agreement with DFT calculations. These results show the promise of the use of metallohelicates as suitable systems for the selective encapsulation of specific anions in solution.

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
Ni2]超分子螺旋体的客体选择性
本研究制备并描述了两种新的顺磁性超分子螺旋体,其化学式为 (X@[Ni2L3])3+(X = Cl 或 Br;L = 双吡唑吡啶配体)。这种金属的螺旋状化合物非常罕见,几乎没有作为阴离子物种宿主的实例。质谱法和顺磁核磁共振法明确证明了这种新组装体在溶液中的持久性。这使得配位[Ni2]宿主对 Cl- 而非 Br- 的偏好得以确定,这与 DFT 计算结果一致。这些结果表明,使用金属杂环化合物作为合适的体系来选择性地封装溶液中的特定阴离子是大有可为的。
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
Nanoscale layer-separated zincophosphate framework enabled by dual-mode aromatic pillar engineering for selective luminescent dye detection. Aluminum dihydride from E(IV) precursors (E = Si, Ge) and its bond-activation reactivities. Structural design principles for hybrid cadmium thiocyanate-halides containing bulky organic cations. Hydration-driven Structural Reorganization and Switchable Thermal-Photoinduced Spin-State Dynamics in Iron(II) Spin-crossover Crystalline Solids Effect of Al doping on the microwave absorption performance of 1T/2H heterogeneous interface MoSe2
×
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:604180095
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