Marta Orts-Arroyo, , , Adrián Sanchis-Perucho, , , Paula León-Barcenas, , , Mario Pacheco, , , Nicolás Moliner, , , Ànnia Tubau, , , Júlia Mayans*, , , Renato Rabelo, , , Francesc Lloret, , , Isabel Castro*, , , Giovanni De Munno, , , Nadia Marino*, , , Rafael Ruiz-García, , and , José Martínez-Lillo*,
{"title":"Vaporesponsive Lanthanide Metal–Organic Frameworks as Selective Luminescent Spin Quantum Sensors for Biogenic Amines","authors":"Marta Orts-Arroyo, , , Adrián Sanchis-Perucho, , , Paula León-Barcenas, , , Mario Pacheco, , , Nicolás Moliner, , , Ànnia Tubau, , , Júlia Mayans*, , , Renato Rabelo, , , Francesc Lloret, , , Isabel Castro*, , , Giovanni De Munno, , , Nadia Marino*, , , Rafael Ruiz-García, , and , José Martínez-Lillo*, ","doi":"10.1021/acs.inorgchem.5c02892","DOIUrl":null,"url":null,"abstract":"<p >Detecting biogenic amines (BAs) is a topic of particular interest for future technological applications of metal–organic frameworks (MOFs) in food quality control. Herein, we demonstrate that integrating lanthanide single-ion magnets (SIMs) into MOFs offers a convenient route for developing a new class of luminescent spin quantum sensors for BA sensing, termed Ln SIM-MOFs. This study focuses on the well-known family of lanthanide(III) sesquioxalate hydrates of general formula {[Ln<sup>III</sup><sub>2</sub>(ox)<sub>3</sub>(H<sub>2</sub>O)<sub>6</sub>]·<i>x</i>H<sub>2</sub>O}<sub><i>n</i></sub>, which feature a 2D hexagonal layer structure. Upon selective adsorption of methylamine over di- or trimethylamine vapors, these compounds exhibit either a partial quenching of the luminescence [Ln = Eu <b>1a</b> (<i>x</i> = 3) and Tb <b>2a</b> (<i>x</i> = 3)] or a dramatic change of the spin dynamics from a slower to a faster relaxing phase [Ln = Er <b>3a</b> (<i>x</i> = 2.5)]. The dual luminescent and magnetic vaposwitching behavior observed in this series of dynamic Ln SIM-MOFs offers new design principles to obtain multifunctional and multiresponsive molecular materials for the chemical sensing of volatile organic compounds (VOCs), resulting from industrial procedures or food degradation.</p>","PeriodicalId":40,"journal":{"name":"Inorganic Chemistry","volume":"64 40","pages":"20111–20121"},"PeriodicalIF":4.7000,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.inorgchem.5c02892","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Detecting biogenic amines (BAs) is a topic of particular interest for future technological applications of metal–organic frameworks (MOFs) in food quality control. Herein, we demonstrate that integrating lanthanide single-ion magnets (SIMs) into MOFs offers a convenient route for developing a new class of luminescent spin quantum sensors for BA sensing, termed Ln SIM-MOFs. This study focuses on the well-known family of lanthanide(III) sesquioxalate hydrates of general formula {[LnIII2(ox)3(H2O)6]·xH2O}n, which feature a 2D hexagonal layer structure. Upon selective adsorption of methylamine over di- or trimethylamine vapors, these compounds exhibit either a partial quenching of the luminescence [Ln = Eu 1a (x = 3) and Tb 2a (x = 3)] or a dramatic change of the spin dynamics from a slower to a faster relaxing phase [Ln = Er 3a (x = 2.5)]. The dual luminescent and magnetic vaposwitching behavior observed in this series of dynamic Ln SIM-MOFs offers new design principles to obtain multifunctional and multiresponsive molecular materials for the chemical sensing of volatile organic compounds (VOCs), resulting from industrial procedures or food degradation.
期刊介绍:
Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.