{"title":"Sandwich-Type Single-Molecule Magnets Complexes of Er(III) with Ansa-Cyclooctatetraenyl Ligands†","authors":"You-Song Ding, Qi-Wei Chen, Jia-Qi Huang, Xiao-Fei Zhu, Zhiping Zheng","doi":"10.1002/cjoc.202400600","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Many sandwich-type lanthanide complexes show extremely high energy barriers (<i>U</i><sub>eff</sub>) for the reversal of magnetization and high blocking temperatures, being the star molecules in the research area of single-molecule magnets. Herein, the preparation, structural determination, and magnetic property studies of two <i>ansa</i>-bridged Er-COT (COT = cyclooctatetraenyl dianion) complexes [KDME<sub>2</sub>][Er((η<sup>8</sup>-COT-Si<sup>Me2</sup>)<sub>2</sub>O)] (<b>1</b>) and [KDME<sub>2</sub>][Er((η<sup>8</sup>-COT-Si<sup><i>i</i>Pr2</sup>)<sub>2</sub>O)]K[Er((η<sup>8</sup>-COT-Si<sup><i>i</i>Pr2</sup>)<sub>2</sub>O)] (<b>2</b>) were reported. The Er(III) ions in both complexes are sandwiched by two COT rings which are <i>ansa</i>-bridged by a [Si-O-Si] group. Magnetic studies reveal both complexes display slow magnetic relaxations with comparable energy barriers (228(5) K for <b>1</b>, and 196(4) K for <b>2</b>) and blocking temperatures (10.5 K for both complexes). The difference in the relaxation times (<i>τ</i>) for the two complexes was studied in details: different molecular vibrations induced by the substituents are the main reason for <i>τ</i> for <b>1</b> being about 10 times longer than for <b>2</b> at the same temperature above 10 K, while the quantum tunnelling of magnetization relaxation time (<i>τ</i><sub>QTM</sub>) for <b>2</b> is about 10 times longer than for <b>1</b> below 8 K, probably owing to the different dipolar interactions. Further rearrangement of molecular network with such <i>ansa</i>-bridged SMMs is promising to design molecular magnetic materials with enhanced properties or new properties.</p>\n <p>\n </p>\n </div>","PeriodicalId":151,"journal":{"name":"Chinese Journal of Chemistry","volume":"42 23","pages":"3099-3106"},"PeriodicalIF":5.5000,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cjoc.202400600","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Many sandwich-type lanthanide complexes show extremely high energy barriers (Ueff) for the reversal of magnetization and high blocking temperatures, being the star molecules in the research area of single-molecule magnets. Herein, the preparation, structural determination, and magnetic property studies of two ansa-bridged Er-COT (COT = cyclooctatetraenyl dianion) complexes [KDME2][Er((η8-COT-SiMe2)2O)] (1) and [KDME2][Er((η8-COT-SiiPr2)2O)]K[Er((η8-COT-SiiPr2)2O)] (2) were reported. The Er(III) ions in both complexes are sandwiched by two COT rings which are ansa-bridged by a [Si-O-Si] group. Magnetic studies reveal both complexes display slow magnetic relaxations with comparable energy barriers (228(5) K for 1, and 196(4) K for 2) and blocking temperatures (10.5 K for both complexes). The difference in the relaxation times (τ) for the two complexes was studied in details: different molecular vibrations induced by the substituents are the main reason for τ for 1 being about 10 times longer than for 2 at the same temperature above 10 K, while the quantum tunnelling of magnetization relaxation time (τQTM) for 2 is about 10 times longer than for 1 below 8 K, probably owing to the different dipolar interactions. Further rearrangement of molecular network with such ansa-bridged SMMs is promising to design molecular magnetic materials with enhanced properties or new properties.
期刊介绍:
The Chinese Journal of Chemistry is an international forum for peer-reviewed original research results in all fields of chemistry. Founded in 1983 under the name Acta Chimica Sinica English Edition and renamed in 1990 as Chinese Journal of Chemistry, the journal publishes a stimulating mixture of Accounts, Full Papers, Notes and Communications in English.