Thorfinnur Gunnlaugsson, Ena Thea Luis, Tumpa Gorai, June Lovitt, Brendan Twamley
{"title":"基于分层镧系元素的自组装复合物在竞争介质中对温度变化和化学反应都有可逆的发光响应","authors":"Thorfinnur Gunnlaugsson, Ena Thea Luis, Tumpa Gorai, June Lovitt, Brendan Twamley","doi":"10.1039/d5dt00831j","DOIUrl":null,"url":null,"abstract":"Here we report hierarchical self-assembly formation of luminescent Eu3+-1-DPA complex in mixed aqueous-organic (THF or ethanol) solutions and its reversible responsive behaviour to temperature change and in situ chemical reactions were investigated. The ligands 1-DPA and 1-DPA-acetate as well as the Eu(III) complex of 1-DPA, Eu3+-1-DPA were synthesised, as well as their X-ray crystal structures were determined. The photophysical and material (morphological) properties of the ligands and the Eu(III) complexes formed in situ of both 1-DPA and 1-DPA-acetate were probed in mixed aqueous-organic (THF or ethanol) solutions. The ligands as well as the complexes were shown to aggregate into hierarchical and homogenously formed microspheres and microrods, as demonstrated by carrying out SEM imaging of the drop cast solutions of these complexes in ethanol-water mixtures. The Eu3+-1-DPA complex gave rise to Eu(III) centred emission [due to deactivation of the 5D0 7FJ (J = 1-4)], which showed reversible, thermo-responsive lanthanide centred emission, while in situ esterification using acidic anhydride (forming Eu3+-1-DPA-acetate, which was not emissive), and subsequent NaOH mediated hydrolysis of the Eu3+-1-DPA-acetate assembly induced both Eu(III)-emission and morphology changes as demonstrated using both spectroscopic and SEM imaging studies.","PeriodicalId":71,"journal":{"name":"Dalton Transactions","volume":"42 1","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hierarchical lanthanide based self-assembly complexes that undergo reversible luminescent response to both temperature changes and chemical reactions within competitive media\",\"authors\":\"Thorfinnur Gunnlaugsson, Ena Thea Luis, Tumpa Gorai, June Lovitt, Brendan Twamley\",\"doi\":\"10.1039/d5dt00831j\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Here we report hierarchical self-assembly formation of luminescent Eu3+-1-DPA complex in mixed aqueous-organic (THF or ethanol) solutions and its reversible responsive behaviour to temperature change and in situ chemical reactions were investigated. The ligands 1-DPA and 1-DPA-acetate as well as the Eu(III) complex of 1-DPA, Eu3+-1-DPA were synthesised, as well as their X-ray crystal structures were determined. The photophysical and material (morphological) properties of the ligands and the Eu(III) complexes formed in situ of both 1-DPA and 1-DPA-acetate were probed in mixed aqueous-organic (THF or ethanol) solutions. The ligands as well as the complexes were shown to aggregate into hierarchical and homogenously formed microspheres and microrods, as demonstrated by carrying out SEM imaging of the drop cast solutions of these complexes in ethanol-water mixtures. The Eu3+-1-DPA complex gave rise to Eu(III) centred emission [due to deactivation of the 5D0 7FJ (J = 1-4)], which showed reversible, thermo-responsive lanthanide centred emission, while in situ esterification using acidic anhydride (forming Eu3+-1-DPA-acetate, which was not emissive), and subsequent NaOH mediated hydrolysis of the Eu3+-1-DPA-acetate assembly induced both Eu(III)-emission and morphology changes as demonstrated using both spectroscopic and SEM imaging studies.\",\"PeriodicalId\":71,\"journal\":{\"name\":\"Dalton Transactions\",\"volume\":\"42 1\",\"pages\":\"\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-05-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Dalton Transactions\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5dt00831j\",\"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":"Dalton Transactions","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5dt00831j","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Hierarchical lanthanide based self-assembly complexes that undergo reversible luminescent response to both temperature changes and chemical reactions within competitive media
Here we report hierarchical self-assembly formation of luminescent Eu3+-1-DPA complex in mixed aqueous-organic (THF or ethanol) solutions and its reversible responsive behaviour to temperature change and in situ chemical reactions were investigated. The ligands 1-DPA and 1-DPA-acetate as well as the Eu(III) complex of 1-DPA, Eu3+-1-DPA were synthesised, as well as their X-ray crystal structures were determined. The photophysical and material (morphological) properties of the ligands and the Eu(III) complexes formed in situ of both 1-DPA and 1-DPA-acetate were probed in mixed aqueous-organic (THF or ethanol) solutions. The ligands as well as the complexes were shown to aggregate into hierarchical and homogenously formed microspheres and microrods, as demonstrated by carrying out SEM imaging of the drop cast solutions of these complexes in ethanol-water mixtures. The Eu3+-1-DPA complex gave rise to Eu(III) centred emission [due to deactivation of the 5D0 7FJ (J = 1-4)], which showed reversible, thermo-responsive lanthanide centred emission, while in situ esterification using acidic anhydride (forming Eu3+-1-DPA-acetate, which was not emissive), and subsequent NaOH mediated hydrolysis of the Eu3+-1-DPA-acetate assembly induced both Eu(III)-emission and morphology changes as demonstrated using both spectroscopic and SEM imaging studies.
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.