Syntheses and magnetic properties of substituted bis-indacenyl bi-metallic complexes & application

Amshumali K. Mungalimane, K.M. Sateesha, K. Mussuvir Pasha, Yuvaraja Dibdalli, Mallikarjun V. Patil, V. Siruguri, R. Reddy
{"title":"Syntheses and magnetic properties of substituted bis-indacenyl bi-metallic complexes & application","authors":"Amshumali K. Mungalimane, K.M. Sateesha, K. Mussuvir Pasha, Yuvaraja Dibdalli, Mallikarjun V. Patil, V. Siruguri, R. Reddy","doi":"10.15446/rev.colomb.quim.v51n1.101889","DOIUrl":null,"url":null,"abstract":"Organometallic compounds, Bis (2,4,6,8 teramethyl-indacenyl) di Iron (1), Bis (2,4,6,8 teramethyl s-indacenyl) mono iron, mono cobalt (2), and Bis (2,6 diethyl-4,8-dimethyl-s-indacenyl) di cobalt (3) were synthesised by means of salt elimination strategy, using Fe(II) and Co(II) salts. The compounds were characterised through spectroscopic and electrochemical methods. Magnetic measurements were carried out by Physical Property Measurement System (PPMS). Mossbauer spectroscopic data reveals that in all compounds, surprisingly, Iron is in +3 oxidation state. DFT calculations have been carried out to understand the change in the oxidation state of a metal. DFT study confirms the electron transfer nature of ligand to metal. Cyclic voltametric study on these compounds shows a large separation (ΔE>800mV) between two oxidation peaks confirming the strong interaction between the metal centres.  Magnetic measurements on these organometallic compounds reveals that they exhibit a ferrimagnetic behaviour at temperatures below 40 K.","PeriodicalId":0,"journal":{"name":"","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15446/rev.colomb.quim.v51n1.101889","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

Organometallic compounds, Bis (2,4,6,8 teramethyl-indacenyl) di Iron (1), Bis (2,4,6,8 teramethyl s-indacenyl) mono iron, mono cobalt (2), and Bis (2,6 diethyl-4,8-dimethyl-s-indacenyl) di cobalt (3) were synthesised by means of salt elimination strategy, using Fe(II) and Co(II) salts. The compounds were characterised through spectroscopic and electrochemical methods. Magnetic measurements were carried out by Physical Property Measurement System (PPMS). Mossbauer spectroscopic data reveals that in all compounds, surprisingly, Iron is in +3 oxidation state. DFT calculations have been carried out to understand the change in the oxidation state of a metal. DFT study confirms the electron transfer nature of ligand to metal. Cyclic voltametric study on these compounds shows a large separation (ΔE>800mV) between two oxidation peaks confirming the strong interaction between the metal centres.  Magnetic measurements on these organometallic compounds reveals that they exhibit a ferrimagnetic behaviour at temperatures below 40 K.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
取代双茚二烯基双金属配合物的合成、磁性及应用
使用Fe(II)和Co(II)盐,通过盐消除策略合成了有机金属化合物,双(2,4,6,8-四甲基-茚三烯基)二铁(1)、双(2、4,6,8-四甲基-s-茚二烯基)单铁、单钴(2)和双(2。6二乙基-4,8-二甲基-s-吲三烯酰基)二钴(3)。通过光谱和电化学方法对化合物进行了表征。通过物理性能测量系统(PPMS)进行磁性测量。穆斯堡尔谱数据显示,令人惊讶的是,在所有化合物中,铁都处于+3氧化态。已经进行DFT计算以了解金属氧化态的变化。DFT研究证实了配体向金属的电子转移性质。对这些化合物的循环伏安法研究表明,两个氧化峰之间有很大的分离(ΔE>800mV),证实了金属中心之间的强烈相互作用。对这些有机金属化合物的磁性测量表明,它们在低于40 K的温度下表现出铁磁性行为。
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
×
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