A High-Toughness NDI-Based Fluorescent Polyurea Based on Gradient Energy Dissipation

IF 5.2 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2025-04-13 DOI:10.1021/acs.macromol.4c02637
Pengcheng Li, Hongzhe Zhao, Zelin Liu, Yanqing Wang, Picheng Chen, Yuetao Liu, Fengchen Qiao, Li Ding, Chuanhui Gao
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Abstract

1,5-Naphthalene diisocyanate (NDI) has garnered considerable attention in the design of functional materials due to its excellent photophysical properties and corrosion resistance. However, materials synthesized from NDI typically exhibit poor toughness, limiting their broader applications. To overcome these limitations, this study synthesized a polyurea material that combines both high toughness and fluorescence properties by constructing the polymer backbone through the rapid reaction of NDI with amines, followed by covalent cross-linking between hard domains. The material demonstrates a mechanical strength of 24.8 MPa and an ultrahigh toughness of 505.25 MJ/m3. Its exceptional toughness stems from a gradient energy dissipation mechanism, which is governed by the dissociation of strong and weak hydrogen bonds (with bond dissociation energies of 76.64 kJ/mol and 64.89 kJ/mol, respectively) and the decomposition of concentrated hard domains. Additionally, the naphthalene rings in NDI possess a planar rigid conjugated structure, and through covalent cross-linking among hard domains, the nonradiative transition is restricted, and the radiative transition is augmented, thereby enabling the material to exhibit intense and stable blue fluorescence under 365 nm UV lamps. The material can still fluoresce in the presence of a strong acid and a strong base, where the strong base enhances the fluorescence intensity, while the strong acid has the opposite effect. By modifying the form of the urea group surrounding the naphthalene ring, the acid–base effect influences the distribution of the electron cloud of the naphthalene ring and subsequently alters the fluorescence intensity. This study offers a novel concept for preparing NDI-based polyurea materials with high toughness and stable fluorescence properties.

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基于梯度耗能的高韧性ndi荧光聚脲
1,5-萘二异氰酸酯(NDI)由于其优异的光物理性能和耐腐蚀性,在功能材料的设计中受到了广泛的关注。然而,由NDI合成的材料通常表现出较差的韧性,限制了其更广泛的应用。为了克服这些限制,本研究通过NDI与胺的快速反应构建聚合物骨架,然后在硬结构域之间进行共价交联,合成了一种兼具高韧性和荧光性能的聚脲材料。该材料的机械强度为24.8 MPa,超高韧性为505.25 MJ/m3。其优异的韧性源于一种梯度能量耗散机制,该机制由强氢键和弱氢键的离解(键离解能分别为76.64 kJ/mol和64.89 kJ/mol)和集中硬畴的分解所控制。此外,NDI中的萘环具有平面刚性共轭结构,通过硬畴之间的共价交联,限制了非辐射跃迁,增强了辐射跃迁,从而使材料在365 nm紫外灯下表现出强烈而稳定的蓝色荧光。该材料在强酸和强碱存在下仍能发出荧光,其中强碱增强荧光强度,强酸则相反。酸碱效应通过改变萘环周围脲基的形态,影响萘环电子云的分布,进而改变荧光强度。本研究为制备具有高韧性和稳定荧光性能的ndi基聚脲材料提供了新的思路。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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