Synthesis, Characterization, and Magnetism of µ‐2‐Chloroterephthalato‐Bridged Binuclear Lanthanide(III) Complexes

Cui‐Wei Yan, Yan-Tuan Li, Chunyuan Zhu
{"title":"Synthesis, Characterization, and Magnetism of µ‐2‐Chloroterephthalato‐Bridged Binuclear Lanthanide(III) Complexes","authors":"Cui‐Wei Yan, Yan-Tuan Li, Chunyuan Zhu","doi":"10.1081/SIM-120037519","DOIUrl":null,"url":null,"abstract":"Abstract Nine new binuclear lanthanide(III) complexes described by the overall formula [Ln2(CTPHA)(Me2bpy)4(ClO4)2](ClO4)2 (Ln = Y, La, Nd, Eu, Gd, Tb, Dy, Ho, Er; Me2bpy = 4,4′‐dimethyl‐2,2′‐bipyridine; and CTPHA = 2‐chloroterephthalate dianion), have been synthesized and characterized by elemental analyses, molar conductance measurements, and IR, ESR, and electronic spectra studies. It is proposed that these complexes have CTPHA‐bridged structures consisting of two lanthanide(III) ions. The variable‐temperature magnetic susceptibility (4–300 K) of [Gd2(CTPHA)(Me2bpy)4(ClO4)2](ClO4)2 was further measured and the magnetic analysis was carried out by means of a least‐square method to fit the observed data with the susceptibility equation derived from the spin Hamiltonian operator, Ĥ = −2J Ŝ 1 Ŝ 2, giving the exchange parameter J = −0.12 cm−1. This result indicates that the operation of a very weak antiferromagnetic spin‐exchange interaction between the adjacent gadolinium(III) and gadolinium(III) ions within the complex.","PeriodicalId":22160,"journal":{"name":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","volume":"13 1","pages":"953 - 966"},"PeriodicalIF":0.0000,"publicationDate":"2004-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthesis and Reactivity in Inorganic and Metal-organic Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1081/SIM-120037519","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Abstract Nine new binuclear lanthanide(III) complexes described by the overall formula [Ln2(CTPHA)(Me2bpy)4(ClO4)2](ClO4)2 (Ln = Y, La, Nd, Eu, Gd, Tb, Dy, Ho, Er; Me2bpy = 4,4′‐dimethyl‐2,2′‐bipyridine; and CTPHA = 2‐chloroterephthalate dianion), have been synthesized and characterized by elemental analyses, molar conductance measurements, and IR, ESR, and electronic spectra studies. It is proposed that these complexes have CTPHA‐bridged structures consisting of two lanthanide(III) ions. The variable‐temperature magnetic susceptibility (4–300 K) of [Gd2(CTPHA)(Me2bpy)4(ClO4)2](ClO4)2 was further measured and the magnetic analysis was carried out by means of a least‐square method to fit the observed data with the susceptibility equation derived from the spin Hamiltonian operator, Ĥ = −2J Ŝ 1 Ŝ 2, giving the exchange parameter J = −0.12 cm−1. This result indicates that the operation of a very weak antiferromagnetic spin‐exchange interaction between the adjacent gadolinium(III) and gadolinium(III) ions within the complex.
µ‐2‐氯对苯二甲酸桥联双核镧系(III)配合物的合成、表征和磁性研究
用总式[Ln2(CTPHA)(Me2bpy)4(ClO4)2](ClO4)2 (Ln = Y, La, Nd, Eu, Gd, Tb, Dy, Ho, Er)描述的九种新型双核镧系(III)配合物;Me2bpy = 4,4′‐二甲基‐2,2′‐联吡啶;和CTPHA = 2‐氯对苯二甲酸二钠),已经合成并通过元素分析,摩尔电导测量,IR, ESR和电子光谱研究进行了表征。提出这些配合物具有由两个镧系(III)离子组成的CTPHA -桥接结构。进一步测量了[Gd2(CTPHA)(Me2bpy)4(ClO4)2](ClO4)2的变温磁化率(4 - 300 K),并用最小二乘法将观测数据与自旋哈密顿算子推导的磁化率方程Ĥ =−2J Ŝ 1 Ŝ 2拟合,得到交换参数J =−0.12 cm−1。这一结果表明配合物内相邻的钆(III)和钆(III)离子之间存在非常弱的反铁磁自旋交换相互作用。
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
自引率
0.00%
发文量
0
×
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