Ying-Juan Wei, Yi-Cong Lou, Shu-Ying Luo, Qing-Hu Teng, Fu-Pei Liang, Kai Wang
{"title":"8-羟基喹啉超分子堆积镝配合物的合成、结构和磁性研究","authors":"Ying-Juan Wei, Yi-Cong Lou, Shu-Ying Luo, Qing-Hu Teng, Fu-Pei Liang, Kai Wang","doi":"10.1016/j.ica.2025.122828","DOIUrl":null,"url":null,"abstract":"<div><div>In this work, we report three Dy<sup>III</sup> complexes, namely, [Dy<sub>3</sub>(ql)<sub>8</sub>Cl(Hql)]·3CH<sub>3</sub>OH·H<sub>2</sub>O (<strong>1</strong>; Hql = 8-hydroxyquinoline), [Dy<sub>3</sub>(ql)<sub>7</sub>(NO<sub>3</sub>)<sub>2</sub>(Hql)]·3CH<sub>3</sub>CN (<strong>2</strong>) and [Dy<sub>2</sub>(ql)<sub>3</sub>(Xa)(NO<sub>3</sub>)<sub>2</sub>(CH<sub>3</sub>OH)<sub>2</sub>(H<sub>2</sub>O)] (<strong>3</strong>, HXa = xanthene-9-carboxylic acid). Both <strong>1</strong> and <strong>2</strong> feature quasi-linear trinuclear cluster structures, while <strong>3</strong> has a dinuclear structure. Significantly, diverse intermolecular π-π interactions led to the structural variety in three systems, forming supermolecular dimers of <strong>1</strong> and <strong>3</strong>, and a supramolecular 2D honeycomb-like framework of <strong>2</strong>. Magnetic studies demonstrate that <strong>1</strong> and <strong>3</strong> exhibit field induced dual relaxation behavior. The efficient energy barriers for their slow relaxation processes are only 3.0 and 2.1 K. In contrast, <strong>2</strong> displays zero-field relaxation behavior, with an efficient energy barrier of 140 K. This work highlights how ligand field engineering and π-π stacking interactions synergistically modulate relaxation dynamics in lanthanoid single-molecule magnets systems.</div></div>","PeriodicalId":13599,"journal":{"name":"Inorganica Chimica Acta","volume":"587 ","pages":"Article 122828"},"PeriodicalIF":2.7000,"publicationDate":"2025-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis, structures and magnetic properties of π-stacked supermolecular dysprosium(III) complexes with 8-hydroxyquinoline\",\"authors\":\"Ying-Juan Wei, Yi-Cong Lou, Shu-Ying Luo, Qing-Hu Teng, Fu-Pei Liang, Kai Wang\",\"doi\":\"10.1016/j.ica.2025.122828\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In this work, we report three Dy<sup>III</sup> complexes, namely, [Dy<sub>3</sub>(ql)<sub>8</sub>Cl(Hql)]·3CH<sub>3</sub>OH·H<sub>2</sub>O (<strong>1</strong>; Hql = 8-hydroxyquinoline), [Dy<sub>3</sub>(ql)<sub>7</sub>(NO<sub>3</sub>)<sub>2</sub>(Hql)]·3CH<sub>3</sub>CN (<strong>2</strong>) and [Dy<sub>2</sub>(ql)<sub>3</sub>(Xa)(NO<sub>3</sub>)<sub>2</sub>(CH<sub>3</sub>OH)<sub>2</sub>(H<sub>2</sub>O)] (<strong>3</strong>, HXa = xanthene-9-carboxylic acid). Both <strong>1</strong> and <strong>2</strong> feature quasi-linear trinuclear cluster structures, while <strong>3</strong> has a dinuclear structure. Significantly, diverse intermolecular π-π interactions led to the structural variety in three systems, forming supermolecular dimers of <strong>1</strong> and <strong>3</strong>, and a supramolecular 2D honeycomb-like framework of <strong>2</strong>. Magnetic studies demonstrate that <strong>1</strong> and <strong>3</strong> exhibit field induced dual relaxation behavior. The efficient energy barriers for their slow relaxation processes are only 3.0 and 2.1 K. In contrast, <strong>2</strong> displays zero-field relaxation behavior, with an efficient energy barrier of 140 K. This work highlights how ligand field engineering and π-π stacking interactions synergistically modulate relaxation dynamics in lanthanoid single-molecule magnets systems.</div></div>\",\"PeriodicalId\":13599,\"journal\":{\"name\":\"Inorganica Chimica Acta\",\"volume\":\"587 \",\"pages\":\"Article 122828\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-06-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganica Chimica Acta\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0020169325002944\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganica Chimica Acta","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0020169325002944","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Synthesis, structures and magnetic properties of π-stacked supermolecular dysprosium(III) complexes with 8-hydroxyquinoline
In this work, we report three DyIII complexes, namely, [Dy3(ql)8Cl(Hql)]·3CH3OH·H2O (1; Hql = 8-hydroxyquinoline), [Dy3(ql)7(NO3)2(Hql)]·3CH3CN (2) and [Dy2(ql)3(Xa)(NO3)2(CH3OH)2(H2O)] (3, HXa = xanthene-9-carboxylic acid). Both 1 and 2 feature quasi-linear trinuclear cluster structures, while 3 has a dinuclear structure. Significantly, diverse intermolecular π-π interactions led to the structural variety in three systems, forming supermolecular dimers of 1 and 3, and a supramolecular 2D honeycomb-like framework of 2. Magnetic studies demonstrate that 1 and 3 exhibit field induced dual relaxation behavior. The efficient energy barriers for their slow relaxation processes are only 3.0 and 2.1 K. In contrast, 2 displays zero-field relaxation behavior, with an efficient energy barrier of 140 K. This work highlights how ligand field engineering and π-π stacking interactions synergistically modulate relaxation dynamics in lanthanoid single-molecule magnets systems.
期刊介绍:
Inorganica Chimica Acta is an established international forum for all aspects of advanced Inorganic Chemistry. Original papers of high scientific level and interest are published in the form of Articles and Reviews.
Topics covered include:
• chemistry of the main group elements and the d- and f-block metals, including the synthesis, characterization and reactivity of coordination, organometallic, biomimetic, supramolecular coordination compounds, including associated computational studies;
• synthesis, physico-chemical properties, applications of molecule-based nano-scaled clusters and nanomaterials designed using the principles of coordination chemistry, as well as coordination polymers (CPs), metal-organic frameworks (MOFs), metal-organic polyhedra (MPOs);
• reaction mechanisms and physico-chemical investigations computational studies of metalloenzymes and their models;
• applications of inorganic compounds, metallodrugs and molecule-based materials.
Papers composed primarily of structural reports will typically not be considered for publication.