Encage the Carcinogens: A Metal–“Organic Cage” Framework for Efficient Polycyclic Aromatic Hydrocarbon Removal From Water

IF 13 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Small Pub Date : 2024-12-02 DOI:10.1002/smll.202408482
Bhaswati Paul, Sandipan Ghorai, Jayanta Samanta, Ramalingam Natarajan
{"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":"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.","PeriodicalId":228,"journal":{"name":"Small","volume":"74 1","pages":""},"PeriodicalIF":13.0000,"publicationDate":"2024-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://doi.org/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

Abstract

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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
求助全文
约1分钟内获得全文 去求助
来源期刊
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
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.
期刊最新文献
Oxygen‐Assisted Tailoring of Evaporated PbS Hole Transport Layer for Highly Efficient Antimony Sulfide Solar Cells Effect of Different Molten Salts on Structure and Water Splitting Performance of Al‐Doped Fillet Polyhedral SrTiO3 Encage the Carcinogens: A Metal–“Organic Cage” Framework for Efficient Polycyclic Aromatic Hydrocarbon Removal From Water Introducing Degradable Cationic Nanogels Carrying TLR9 Stimulating Oligonucleotides Renovating Stability and Performance in Magnetorheological Fluids Through Particle Size and Shape Anisotropy
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1