{"title":"包住致癌物:一种金属-“有机笼”框架,用于从水中高效去除多环芳烃","authors":"Bhaswati Paul, Sandipan Ghorai, Jayanta Samanta, Ramalingam Natarajan","doi":"10.1002/smll.202408482","DOIUrl":null,"url":null,"abstract":"<p>Polycyclic aromatic hydrocarbons (PAHs) are carcinogenic and persistent organic pollutants in water. Their removal is highly challenging for existing generic and nonspecific adsorbents, creating an urgent need for tailored solutions. Herein, a metal-“organic cage” framework, <b>MOF-CC-1</b>, designed for the effective scavenging of PAHs from water is is introduced. This framework is constructed using a propeller-shaped cofacial organic cage (<b>CC-1</b>), equipped with three triazole pillars that coordinate with Ag(I) ions. The cationic <b>MOF-CC-1</b> adopts a chiral (10,3)-a <b>srs</b> net structure, spontaneously resolving into homochiral crystals. Additionally, bulk homochirality is achieved through chirality induction using chiral counteranions. <b>MOF-CC-1</b> uniquely encapsulates diverse PAH molecules within the cavities of CC-1, as confirmed by single-crystal X-ray diffraction, marking it as the first metal–“organic cage” framework with structural evidence of guest inclusion inside the organic cage linker. Further, <b>MOF-CC-1</b> exhibits soft porosity, remaining nonporous to N₂ gas when compressed but expanding to encapsulate PAHs in solution. Moreover, <b>MOF-CC-1</b> exhibits exceptional efficacy in scavenging ppb levels of PAHs from water. This work represents a significant advancement in utilizing organic cages as ligands toward MOF construction, paving the way for tailored adsorbents for PAH removal, and addressing a critical need for selective and efficient materials in environmental remediation.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"21 7","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Encage the Carcinogens: A Metal–“Organic Cage” Framework for Efficient Polycyclic Aromatic Hydrocarbon Removal From Water\",\"authors\":\"Bhaswati Paul, Sandipan Ghorai, Jayanta Samanta, Ramalingam Natarajan\",\"doi\":\"10.1002/smll.202408482\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Polycyclic aromatic hydrocarbons (PAHs) are carcinogenic and persistent organic pollutants in water. Their removal is highly challenging for existing generic and nonspecific adsorbents, creating an urgent need for tailored solutions. Herein, a metal-“organic cage” framework, <b>MOF-CC-1</b>, designed for the effective scavenging of PAHs from water is is introduced. This framework is constructed using a propeller-shaped cofacial organic cage (<b>CC-1</b>), equipped with three triazole pillars that coordinate with Ag(I) ions. The cationic <b>MOF-CC-1</b> adopts a chiral (10,3)-a <b>srs</b> net structure, spontaneously resolving into homochiral crystals. Additionally, bulk homochirality is achieved through chirality induction using chiral counteranions. <b>MOF-CC-1</b> uniquely encapsulates diverse PAH molecules within the cavities of CC-1, as confirmed by single-crystal X-ray diffraction, marking it as the first metal–“organic cage” framework with structural evidence of guest inclusion inside the organic cage linker. Further, <b>MOF-CC-1</b> exhibits soft porosity, remaining nonporous to N₂ gas when compressed but expanding to encapsulate PAHs in solution. Moreover, <b>MOF-CC-1</b> exhibits exceptional efficacy in scavenging ppb levels of PAHs from water. This work represents a significant advancement in utilizing organic cages as ligands toward MOF construction, paving the way for tailored adsorbents for PAH removal, and addressing a critical need for selective and efficient materials in environmental remediation.</p>\",\"PeriodicalId\":228,\"journal\":{\"name\":\"Small\",\"volume\":\"21 7\",\"pages\":\"\"},\"PeriodicalIF\":12.1000,\"publicationDate\":\"2024-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Small\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/smll.202408482\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202408482","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
多环芳烃(PAHs)是水中的致癌性和持久性有机污染物。对于现有的通用和非特异性吸附剂来说,它们的去除非常具有挑战性,因此迫切需要定制解决方案。本文介绍了一种金属-“有机笼”框架,MOF - CC - 1,设计用于有效清除水中的多环芳烃。该框架使用螺旋桨形共面有机笼(CC‐1)构建,配备三个与Ag(I)离子配合的三唑柱。阳离子MOF‐CC‐1采用手性(10,3)‐a srs网状结构,自发分解成同手性晶体。此外,通过使用手性反阴离子进行手性诱导,获得了体同手性。单晶X射线衍射证实,MOF‐CC‐1独特地将多种多环芳烃分子封装在CC‐1的空腔内,标志着它是第一个金属“有机笼”框架,在有机笼连接剂中有客体包裹的结构证据。此外,MOF‐CC‐1表现出软孔隙性,在压缩时对n2气体保持无孔性,但在溶液中膨胀以封装多环芳烃。此外,MOF‐CC‐1在清除水中ppb水平的多环芳烃方面表现出卓越的功效。这项工作代表了利用有机笼作为MOF结构配体的重大进展,为去除多环芳烃的定制吸附剂铺平了道路,并解决了环境修复中对选择性和高效材料的迫切需求。
Encage the Carcinogens: A Metal–“Organic Cage” Framework for Efficient Polycyclic Aromatic Hydrocarbon Removal From Water
Polycyclic aromatic hydrocarbons (PAHs) are carcinogenic and persistent organic pollutants in water. Their removal is highly challenging for existing generic and nonspecific adsorbents, creating an urgent need for tailored solutions. Herein, a metal-“organic cage” framework, MOF-CC-1, designed for the effective scavenging of PAHs from water is is introduced. This framework is constructed using a propeller-shaped cofacial organic cage (CC-1), equipped with three triazole pillars that coordinate with Ag(I) ions. The cationic MOF-CC-1 adopts a chiral (10,3)-a srs net structure, spontaneously resolving into homochiral crystals. Additionally, bulk homochirality is achieved through chirality induction using chiral counteranions. MOF-CC-1 uniquely encapsulates diverse PAH molecules within the cavities of CC-1, as confirmed by single-crystal X-ray diffraction, marking it as the first metal–“organic cage” framework with structural evidence of guest inclusion inside the organic cage linker. Further, MOF-CC-1 exhibits soft porosity, remaining nonporous to N₂ gas when compressed but expanding to encapsulate PAHs in solution. Moreover, MOF-CC-1 exhibits exceptional efficacy in scavenging ppb levels of PAHs from water. This work represents a significant advancement in utilizing organic cages as ligands toward MOF construction, paving the way for tailored adsorbents for PAH removal, and addressing a critical need for selective and efficient materials in environmental remediation.
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology.
Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.