Self-healable functional polymers based on Diels–Alder ‘click chemistry’ involving substituted furan and triazolinedione derivatives: a simple and very fast approach
文献信息
Prantik Mondal, Gourhari Jana, Tuhin Subhra Pal, Nikhil K. Singha
Nowadays, the design of functional polymer materials that can mimic natural phenomena, e.g., the self-healing of skin cuts, has received tremendous interest in materials science and engineering. Recently, 1,2,4-triazoline-3,5-dione (TAD) derivatives have been widely utilized in the functionalization of different functional polymer systems via several ‘click’ approaches within a relatively shorter period at room temperature (r.t.) compared to the widely used conventional furfuryl–maleimide Diels–Alder ‘click chemistry’, which requires elevated temperatures and longer times. In the present investigation, the dynamic DA-click reaction based on 2,5-disubstituted furan (diene) and TAD (dienophile) functionalisation was executed for developing self-healable functional tailor-made polymethacrylates. For this purpose, polymethacrylates bearing 5-methyl-2-furoate pendants (which can act as the ‘click’ partner of the TAD derivative) were prepared via the reversible addition–fragmentation chain transfer (RAFT) polymerization of 2-hydroxyethyl methacrylate (HEMA), followed by the esterification of the hydroxyl groups of poly(2-hydroxyethyl methacrylate) (PHEMA) using 5-methyl-2-furoic acid (MFA). Then, the TAD derivative was added for the DA post-polymerization modification of the polymers containing 2,5-disubstituted furan moieties, which was accomplished within 2 h under ambient conditions. For a better understanding, a model DA reaction using smaller organic molecules (which were analogous to the polymer system) was studied through density functional theory (DFT) based calculations and related spectroscopic analysis. As evidenced by the differential scanning calorimetry (DSC) analysis, the furan–TAD DA σ-bonds were reversible at 130 °C. The thermoreversible nature of the TAD ‘clicked’ bonds induced the self-healing feature within the DA polymethacrylates, which was monitored using different microscopy analyses.
相关文献
Rapid single-cell detection and identification of pathogens by using surface-enhanced Raman spectroscopy
N. E. Dina, H. Zhou, A. Colniţă, N. Leopold, C. Coman, C. Haisch
DOI: 10.1039/C7AN00106A
A reaction-based near-infrared fluorescent probe that can visualize endogenous selenocysteine in vivo in tumor-bearing mice
Xiaoning Kai, Yiran Zhang, Youguang Zheng, Yunsheng Xue, Xiaoxing Yin, Jing Zhao
DOI: 10.1039/C8AN00765A
Direct, uncorrected, molecule-free analysis of 236U from uranium-bearing particles with NAUTILUS: a new kind of mass spectrometer
D. Willingham, E. E. Groopman, K. S. Grabowski, L. Sangely
DOI: 10.1039/C8AN01451E
Spectrophotometric analysis at the single-cell level: elucidating dispersity within melanic immortalized cell populations
Gerardo Gutiérrez-Juárez, David Cywiak, Rafael Pérez-Solano, Gary A. Baker
DOI: 10.1039/C6AN02662A
Structuring polarity-inverted TBA to G-quadruplex for selective recognition of planarity of natural isoquinoline alkaloids
Yufeng Zhou, Yali Yu, Longlong Gao, Yifan Fei, Ting Ye, Qiusha Li, Xiaoshun Zhou, Ning Gan, Yong Shao
DOI: 10.1039/C8AN01561A
Correction: The mechanism and regularity of quenching the effect of bases on fluorophores: the base-quenched probe method
Huihui Mao, Guanghua Luo, Yuxia Zhan, Jun Zhang, Shuang Yao, Yang Yu
DOI: 10.1039/C8AN90083C
Raman spectroscopy in microsurgery: impact of operating microscope illumination sources on data quality and tissue classification
Joannie Desroches, Audrey Laurence, Michael Pinto, Marie-Andrée Tremblay, Kevin Petrecca, Frédéric Leblond
DOI: 10.1039/C6AN02061E
Surfactant exfoliated 2D hexagonal Boron Nitride (2D-hBN) explored as a potential electrochemical sensor for dopamine: surfactants significantly influence sensor capabilities
Aamar F. Khan, Dale A. C. Brownson, Christopher W. Foster, Graham C. Smith, Craig E. Banks
DOI: 10.1039/C7AN00323D
Desktop NMR for structure elucidation and identification of strychnine adulteration
Kawarpal Singh, Bernhard Blümich
DOI: 10.1039/C7AN00020K
您可能还喜欢
(5-氨基吡唑-3-基)乙酸(CAS号:174891-10-2)的物理化学性质是什么?
(5-氨基吡唑-3-基)乙酸是一种无色至白色固体,分子量为174.15 g/mol。它在水中具有较好的溶解性,在有机溶剂中的溶解度较低。该化合物具有较好的反应活...
3-氟-4,5-二氯苯胺(CAS号:35754-38-2)适用哪些法规指南?
3-氟-4,5-二氯苯胺受到多项法规指南的约束,包括但不限于GHS(全球化学品统一分类和标签制度)的危险分类标准、欧盟的REACH法规(注册、评估、授权和限制)...
什么是(R)-(+)-2,2',6,6'-四甲氧基-4,4'-联(二(3,5-二甲苯基基)膦基)-3,3'-二联吡啶(CAS号:442905-33-1)?
这是一种有机化合物,化学名为(R)-(+)-2,2',6,6'-四甲氧基-4,4'-联(二(3,5-二甲苯基基)膦基)-3,3'-二联吡啶,CAS号为44290...
1-氨基-2-氰基萘(CAS号:3100-67-2)应用于哪些行业?
1-氨基-2-氰基萘在医药、聚合物、传感器和半导体等行业中有应用。在医药领域,它可用作中间体合成某些药物。在聚合物行业,它可以用于制备具有特定性能的聚合物。此外...
如何处理含有1-溴-4-(异丙氧基甲基)苯(CAS号:98446-84-5)的废料?
处理含1-溴-4-(异丙氧基甲基)苯的废料时,首先应确保废液收集在防渗漏的容器中,避免泄露。然后,可以考虑采用化学降解法或物理吸附法进行处理。在特定条件下,可通...
6-Chloro-8-(trifluoromethyl)chroman-4-one(CAS号:1344889-75-3)的主要用途是什么?
6-氯-8-三氟甲基-2,3-二氢-4H-色喃-4-酮主要用于有机合成中的中间体,也可作为研究试剂使用。
7-乙氧基-2-萘酚(CAS号:57944-44-2)通常如何合成?
7-乙氧基-2-萘酚通常通过N-乙氧基化反应合成,首先将2-萘酚与乙醇钠在乙醇中反应生成7-乙氧基-2-萘酚钠盐,再通过酸化进一步得到7-乙氧基-2-萘酚。该合...
4-(1,1-二氧硫代吗啉)丁醇(CAS号:59801-41-1)适用哪些法规指南?
该化合物需遵循一系列的法规指南,包括但不限于GHS全球统一分类和标签制度,其分类可能包括易燃液体和可能危害水生环境。在欧洲,还需遵循REACH法规,确保物质和混...
4-甲氧基苄基叠氮甲酸酯(CAS号:25474-85-5)的物理化学性质是什么?
4-甲氧基苄基叠氮甲酸酯是一种无色液体,具有一定的挥发性。其分子量为198.16,熔点为-69°C,沸点为105°C。该化合物在水中溶解度较低,在有机溶剂如乙醇...
如何处理含有4-氯-2-氟嘧啶(CAS号:51422-00-5)的废料?
含有4-氯-2-氟嘧啶的废料应按照危险废物处理。首先,应收集并分类这些废料,避免与其他废物混合。然后,可以采用焚烧处理或者交由专业机构进行处置。在处理过程中,需...
来源期刊
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.










![N-{15-[(2,5-Dioxo-1-pyrrolidinyl)oxy]-15-oxo-3,6,9,12-tetraoxapentadec-1-yl}-2-(2-propyn-1-yloxy)acetamide structure N-{15-[(2,5-Dioxo-1-pyrrolidinyl)oxy]-15-oxo-3,6,9,12-tetraoxapentadec-1-yl}-2-(2-propyn-1-yloxy)acetamide structure](https://cnstatic.chemtradehub.com/structs/210/2101206-92-0-2eb5.webp)



