Supramolecular Janus Nanocylinders: Controlling Their Characteristics by the Self-Assembly Process.

IF 4.2 3区 化学 Q2 POLYMER SCIENCE Macromolecular Rapid Communications Pub Date : 2024-11-20 DOI:10.1002/marc.202400492
Sandra Kalem, David Siefker, Mingsheng Ji, Jean-Michel Guigner, Ralf Schweins, Sandrine Pensec, Jutta Rieger, Laurent Bouteiller, Erwan Nicol, Olivier Colombani
{"title":"Supramolecular Janus Nanocylinders: Controlling Their Characteristics by the Self-Assembly Process.","authors":"Sandra Kalem, David Siefker, Mingsheng Ji, Jean-Michel Guigner, Ralf Schweins, Sandrine Pensec, Jutta Rieger, Laurent Bouteiller, Erwan Nicol, Olivier Colombani","doi":"10.1002/marc.202400492","DOIUrl":null,"url":null,"abstract":"<p><p>Janus NanoRods (JNR) are anisotropic and non-symmetrical colloids with two faces of different chemical composition. They are difficult to prepare because of their nanometric dimensions and strong anisotropy. Recently, a versatile strategy was developed, allowing the formation of JNR relying on the self-assembly in aqueous medium of two polymers end-functionalized with non-symmetrical and complementary hydrogen bonding stickers. However, the supramolecular JNR prepared following this strategy are out-of-equilibrium (frozen) and therefore their characteristics depend on the self-assembly process. The present study elucidates the formation mechanism of the JNR and the parameters of the self-assembly process influencing their characteristics. The polymers are initially dissolved as unimers in DMSO. Dropwise addition of water triggers the rapid assembly of more and more unimers into long nanocylinders that are unable to grow anymore once formed. Consequently, increasing the dropwise addition rate of water hardly impacts the process, whereas lowering the initial polymer concentration in DMSO reduces both the length and proportion of nanocylinders. Increasing temperature during water addition weakens hydrogen bonds, triggering the formation of a mixture of spheres and nanocylinders. Many supramolecular polymer assemblies are frozen in solution and these findings should help understanding how to control their characteristics, allowing to adapt them to a target application.</p>","PeriodicalId":205,"journal":{"name":"Macromolecular Rapid Communications","volume":" ","pages":"e2400492"},"PeriodicalIF":4.2000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecular Rapid Communications","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/marc.202400492","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0

Abstract

Janus NanoRods (JNR) are anisotropic and non-symmetrical colloids with two faces of different chemical composition. They are difficult to prepare because of their nanometric dimensions and strong anisotropy. Recently, a versatile strategy was developed, allowing the formation of JNR relying on the self-assembly in aqueous medium of two polymers end-functionalized with non-symmetrical and complementary hydrogen bonding stickers. However, the supramolecular JNR prepared following this strategy are out-of-equilibrium (frozen) and therefore their characteristics depend on the self-assembly process. The present study elucidates the formation mechanism of the JNR and the parameters of the self-assembly process influencing their characteristics. The polymers are initially dissolved as unimers in DMSO. Dropwise addition of water triggers the rapid assembly of more and more unimers into long nanocylinders that are unable to grow anymore once formed. Consequently, increasing the dropwise addition rate of water hardly impacts the process, whereas lowering the initial polymer concentration in DMSO reduces both the length and proportion of nanocylinders. Increasing temperature during water addition weakens hydrogen bonds, triggering the formation of a mixture of spheres and nanocylinders. Many supramolecular polymer assemblies are frozen in solution and these findings should help understanding how to control their characteristics, allowing to adapt them to a target application.

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
超分子 Janus 纳米圆柱:通过自组装过程控制其特性。
Janus NanoRods(JNR)是一种各向异性的非对称胶体,其两面具有不同的化学成分。由于其纳米尺寸和强烈的各向异性,它们很难制备。最近,人们开发出了一种多功能策略,通过在水介质中自组装两种具有非对称和互补氢键粘合末端功能化的聚合物来形成 JNR。然而,采用这种策略制备的超分子 JNR 是非均衡(冻结)的,因此其特性取决于自组装过程。本研究阐明了 JNR 的形成机制以及影响其特性的自组装过程参数。聚合物最初以单体形式溶解在二甲基亚砜中。滴加水滴会促使越来越多的单聚物快速组装成长的纳米圆柱,这些圆柱一旦形成就无法再生长。因此,提高水的滴加速度几乎不会影响这一过程,而降低二甲基亚砜中的初始聚合物浓度则会减少纳米柱的长度和比例。加水过程中温度升高会减弱氢键,从而引发球体和纳米圆柱体混合体的形成。许多超分子聚合物组装体在溶液中是凝固的,这些发现将有助于了解如何控制它们的特性,从而使它们适应目标应用。
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
Macromolecular Rapid Communications
Macromolecular Rapid Communications 工程技术-高分子科学
CiteScore
7.70
自引率
6.50%
发文量
477
审稿时长
1.4 months
期刊介绍: Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.
期刊最新文献
Large-scale Conformational Changes of Diindole Functional Groups Driven by Cation-π Interactions and the Toughening Mechanism of Thermosets. Recyclable Amphiphilic Magnetic-responsive Mixed-Shell Nanoparticles With High Interfacial Activity Comparable to Janus Particles for Oily Water Purification. Stretchable and Self-Adhesive Conductors for Smart Epidermal Electronics. Swelling-Shrinking Behavior of a Hydrogel with a CO2-Switchable Volume Phase Transition Temperature. The Trade-Off between Dechlorination and Polymerization for Facile Fabrication of Electronic Grade Epoxidized Cardol.
×
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