Lin Geng, Kai Wang, Rui Sun, Chang-Tai Li, Xiao-Ru Li, Meng Zhang, Mei-Hui Yu, Ze Chang, Xian-He Bu
{"title":"Donor–Acceptor Metal–Organic Frameworks Featuring Tunable Triplet States for Multistimulus Responsive Room-Temperature Charge Transfer Phosphorescence","authors":"Lin Geng, Kai Wang, Rui Sun, Chang-Tai Li, Xiao-Ru Li, Meng Zhang, Mei-Hui Yu, Ze Chang, Xian-He Bu","doi":"10.31635/ccschem.024.202404116","DOIUrl":null,"url":null,"abstract":"<p>Room-temperature phosphorescence (RTP) has drawn considerable attention due to its fascinating applications. Herein, we report the achievement of multistimulus responsive RTP by utilizing the customizable donor–acceptor (D–A) metal–organic framework (MOF) platform for charge-transfer (CT)-based triplet state tuning. A succession of electron-rich donors was introduced into the triazine-based electron-deficient framework (<b xmlns:bkstg=\"http://www.atypon.com/backstage-ns\" xmlns:fn=\"http://www.w3.org/2005/xpath-functions\" xmlns:pxje=\"java:com.atypon.frontend.services.impl.PassportXslJavaExtentions\" xmlns:urlutil=\"java:com.atypon.literatum.customization.UrlUtil\" xmlns:xlink=\"http://www.w3.org/1999/xlink\">\n<bold>NKU-Mg-2</bold></b>) to give D–A MOFs (<b xmlns:bkstg=\"http://www.atypon.com/backstage-ns\" xmlns:fn=\"http://www.w3.org/2005/xpath-functions\" xmlns:pxje=\"java:com.atypon.frontend.services.impl.PassportXslJavaExtentions\" xmlns:urlutil=\"java:com.atypon.literatum.customization.UrlUtil\" xmlns:xlink=\"http://www.w3.org/1999/xlink\">\n<bold>A1</bold></b>–<b xmlns:bkstg=\"http://www.atypon.com/backstage-ns\" xmlns:fn=\"http://www.w3.org/2005/xpath-functions\" xmlns:pxje=\"java:com.atypon.frontend.services.impl.PassportXslJavaExtentions\" xmlns:urlutil=\"java:com.atypon.literatum.customization.UrlUtil\" xmlns:xlink=\"http://www.w3.org/1999/xlink\">\n<bold>A3</bold></b>) featuring CT-based emission. Notably, donors are designed and guided by heavy atom effect (–Br) to enhance the spin–orbit coupling, thereby achieving a fine-tuning excited state, resulting in the manipulation of phosphorescence from low temperature (<b xmlns:bkstg=\"http://www.atypon.com/backstage-ns\" xmlns:fn=\"http://www.w3.org/2005/xpath-functions\" xmlns:pxje=\"java:com.atypon.frontend.services.impl.PassportXslJavaExtentions\" xmlns:urlutil=\"java:com.atypon.literatum.customization.UrlUtil\" xmlns:xlink=\"http://www.w3.org/1999/xlink\">\n<bold>A1</bold></b>) to room temperature (<b xmlns:bkstg=\"http://www.atypon.com/backstage-ns\" xmlns:fn=\"http://www.w3.org/2005/xpath-functions\" xmlns:pxje=\"java:com.atypon.frontend.services.impl.PassportXslJavaExtentions\" xmlns:urlutil=\"java:com.atypon.literatum.customization.UrlUtil\" xmlns:xlink=\"http://www.w3.org/1999/xlink\">\n<bold>A2</bold></b>). Moreover, enhanced RTP intensity is further achieved by facilely altering the halogen functionalization (<b xmlns:bkstg=\"http://www.atypon.com/backstage-ns\" xmlns:fn=\"http://www.w3.org/2005/xpath-functions\" xmlns:pxje=\"java:com.atypon.frontend.services.impl.PassportXslJavaExtentions\" xmlns:urlutil=\"java:com.atypon.literatum.customization.UrlUtil\" xmlns:xlink=\"http://www.w3.org/1999/xlink\">\n<bold>A3</bold></b>). The modulated <b xmlns:bkstg=\"http://www.atypon.com/backstage-ns\" xmlns:fn=\"http://www.w3.org/2005/xpath-functions\" xmlns:pxje=\"java:com.atypon.frontend.services.impl.PassportXslJavaExtentions\" xmlns:urlutil=\"java:com.atypon.literatum.customization.UrlUtil\" xmlns:xlink=\"http://www.w3.org/1999/xlink\">\n<bold>A3</bold></b> simultaneously achieves multiple stimulus responses to X-ray, temperature, and oxygen, rendering it a promising candidate for novel optical sensors. This work not only achieves flexible control over the excited state but also presents a novel approach for developing multistimulus responsive intelligent optical materials.</p>","PeriodicalId":9810,"journal":{"name":"CCS Chemistry","volume":"16 1","pages":""},"PeriodicalIF":9.4000,"publicationDate":"2024-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"CCS Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31635/ccschem.024.202404116","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Room-temperature phosphorescence (RTP) has drawn considerable attention due to its fascinating applications. Herein, we report the achievement of multistimulus responsive RTP by utilizing the customizable donor–acceptor (D–A) metal–organic framework (MOF) platform for charge-transfer (CT)-based triplet state tuning. A succession of electron-rich donors was introduced into the triazine-based electron-deficient framework (NKU-Mg-2) to give D–A MOFs (A1–A3) featuring CT-based emission. Notably, donors are designed and guided by heavy atom effect (–Br) to enhance the spin–orbit coupling, thereby achieving a fine-tuning excited state, resulting in the manipulation of phosphorescence from low temperature (A1) to room temperature (A2). Moreover, enhanced RTP intensity is further achieved by facilely altering the halogen functionalization (A3). The modulated A3 simultaneously achieves multiple stimulus responses to X-ray, temperature, and oxygen, rendering it a promising candidate for novel optical sensors. This work not only achieves flexible control over the excited state but also presents a novel approach for developing multistimulus responsive intelligent optical materials.
期刊介绍:
CCS Chemistry, the flagship publication of the Chinese Chemical Society, stands as a leading international chemistry journal based in China. With a commitment to global outreach in both contributions and readership, the journal operates on a fully Open Access model, eliminating subscription fees for contributing authors. Issued monthly, all articles are published online promptly upon reaching final publishable form. Additionally, authors have the option to expedite the posting process through Immediate Online Accepted Article posting, making a PDF of their accepted article available online upon journal acceptance.