Luminescent Co-Assemblies of Donor-Acceptor Dimeric Cyanostilbenes with (Bio)Anionic Polymeric Templates

IF 3.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemistry - An Asian Journal Pub Date : 2024-12-31 DOI:10.1002/asia.202401163
Prof. Supratim Banerjee, Susmit Som, Dr. Sharanabasava D. Hiremath, Richeek Sarkar
{"title":"Luminescent Co-Assemblies of Donor-Acceptor Dimeric Cyanostilbenes with (Bio)Anionic Polymeric Templates","authors":"Prof. Supratim Banerjee,&nbsp;Susmit Som,&nbsp;Dr. Sharanabasava D. Hiremath,&nbsp;Richeek Sarkar","doi":"10.1002/asia.202401163","DOIUrl":null,"url":null,"abstract":"<p>Amphiphilic dimeric cyanostilbenes with two donor-acceptor moieties connected through variable aliphatic linkers displayed aggregation in aqueous media to produce red emissive nano-assemblies. In the presence of anionic biopolymers such as <i>ct</i>DNA and heparin, they formed electrostatically driven co-assemblies with enhanced luminescence. Moreover, due to the chiral nature of the bio-templates DNA and heparin, the co-assemblies demonstrated induced chirality features. Although the central double bond in cyanostilbenes is known to undergo various photochemical conversions, these dimeric donor-acceptor cyanostilbenes, in their self-assembled state, essentially remained photoinactive under UV irradiation. However, in the bio-templated co-assemblies, they showed comparatively higher photo-reactivity, which was especially prominent for the <i>ct</i>DNA based co-assemblies. We also found that these co-assemblies can be used as artificial light-harvesting systems by incorporating acceptor dyes and this led to the generation of amplified emission from the acceptor dyes in the NIR range of the spectrum. Furthermore, the co-assemblies demonstrated selective fluorescence quenching in the presence of metal ions such as Cu<sup>2+</sup> and Fe<sup>2+</sup>, highlighting their potential for metal-ion sensing applications.</p>","PeriodicalId":145,"journal":{"name":"Chemistry - An Asian Journal","volume":"20 5","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2024-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry - An Asian Journal","FirstCategoryId":"1","ListUrlMain":"https://aces.onlinelibrary.wiley.com/doi/10.1002/asia.202401163","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Amphiphilic dimeric cyanostilbenes with two donor-acceptor moieties connected through variable aliphatic linkers displayed aggregation in aqueous media to produce red emissive nano-assemblies. In the presence of anionic biopolymers such as ctDNA and heparin, they formed electrostatically driven co-assemblies with enhanced luminescence. Moreover, due to the chiral nature of the bio-templates DNA and heparin, the co-assemblies demonstrated induced chirality features. Although the central double bond in cyanostilbenes is known to undergo various photochemical conversions, these dimeric donor-acceptor cyanostilbenes, in their self-assembled state, essentially remained photoinactive under UV irradiation. However, in the bio-templated co-assemblies, they showed comparatively higher photo-reactivity, which was especially prominent for the ctDNA based co-assemblies. We also found that these co-assemblies can be used as artificial light-harvesting systems by incorporating acceptor dyes and this led to the generation of amplified emission from the acceptor dyes in the NIR range of the spectrum. Furthermore, the co-assemblies demonstrated selective fluorescence quenching in the presence of metal ions such as Cu2+ and Fe2+, highlighting their potential for metal-ion sensing applications.

Abstract Image

Abstract Image

Abstract Image

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
二聚氰二苯乙烯与(生物)阴离子聚合物模板的发光共组装。
两亲二聚氰二苯乙烯通过可变脂肪族连接体连接两个供体-受体基团,在水介质中显示聚集,产生红色发射纳米组件。在阴离子生物聚合物如ctDNA和肝素的存在下,它们形成了具有增强发光的静电驱动的共组装体。此外,由于生物模板DNA和肝素的手性,共组装表现出诱导手性特征。虽然已知氰基二苯乙烯的中心双键经历各种光化学转化,但这些自组装状态的二聚体氰基二苯乙烯在紫外线照射下基本上保持光活性。然而,在生物模板共组装物中,它们表现出相对较高的光反应性,特别是基于ctDNA的共组装物。我们还发现,通过结合受体染料,这些共组件可以用作人工光收集系统,这导致受体染料在近红外光谱范围内产生放大的发射。此外,共聚物在金属离子(如Cu 2 +和Fe 2 +)存在下表现出选择性荧光猝灭,突出了它们在金属离子传感应用中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Chemistry - An Asian Journal
Chemistry - An Asian Journal 化学-化学综合
CiteScore
7.00
自引率
2.40%
发文量
535
审稿时长
1.3 months
期刊介绍: Chemistry—An Asian Journal is an international high-impact journal for chemistry in its broadest sense. The journal covers all aspects of chemistry from biochemistry through organic and inorganic chemistry to physical chemistry, including interdisciplinary topics. Chemistry—An Asian Journal publishes Full Papers, Communications, and Focus Reviews. A professional editorial team headed by Dr. Theresa Kueckmann and an Editorial Board (headed by Professor Susumu Kitagawa) ensure the highest quality of the peer-review process, the contents and the production of the journal. Chemistry—An Asian Journal is published on behalf of the Asian Chemical Editorial Society (ACES), an association of numerous Asian chemical societies, and supported by the Gesellschaft Deutscher Chemiker (GDCh, German Chemical Society), ChemPubSoc Europe, and the Federation of Asian Chemical Societies (FACS).
期刊最新文献
BX3-Mediated Arene Borylation: Concepts, Scope, and Mechanistic Insight. Metal-Free Strategies for Indoles and o-Acyl Benzanilides From 2-Alkynylaniline Derivatives: Experimental and DFT Insights. Masking Effects of Odorants on a Malodorous Molecule in a Phospholipid Molecular Layer. Toward the Rational Design of Ion-Conducting Ionic Liquid-Incorporated Metal-Organic Framework Hybrids. Naphthalimide-Based Dyed Long Fluorescent Lifetime Probe for Lipid Droplet Viscosity Mapping in Non-Alcoholic Fatty Liver Disease.
×
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:604180095
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