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基于氢键和金属配位的增韧可自愈超分子双聚合物网络

Toughening Healable Supramolecular Double Polymer Networks Based on Hydrogen Bonding and Metal Coordination.

作者信息

Onori Ilaria, Formon Georges J M, Weder Christoph, Augusto Berrocal José

机构信息

Adolphe Merkle Institute, University of Fribourg, Chemin des Verdiers 4, 1700, Fribourg, Switzerland.

NCCR Bio-Inspired Materials, University of Fribourg, 1700, Fribourg, Switzerland.

出版信息

Chemistry. 2024 Dec 23;30(72):e202402511. doi: 10.1002/chem.202402511. Epub 2024 Nov 9.

Abstract

Double polymer networks (DNs) consist of two interpenetrating polymer networks and can offer properties that are not merely a sum of the parts. Here, we report an elastic DN made from two supramolecular polymers (SMPs) that consist of the same poly(n-butyl acrylate) (BA) backbone. The two polymers feature different non-covalent binding motifs, which form dynamic, reversible cross-links. The polymers were prepared by reversible addition-fragmentation chain-transfer polymerization of n-butyl acrylate and either the self-complementary hydrogen-bonding motif 2-ureido-4[1H]pyrimidinone, or the 2,6-bis(1'-methylbenzimidazolyl)pyridine ligand, which forms complexes with metal ions. The supramolecular DN made by these components combines features of the single networks, including high thermal stability and resistance to creep. The DN further exhibits excellent healability and displays a higher extensibility and a higher toughness than its constituents. The mechanical characteristics of the DN can be further enhanced by selectively pre-stretching one of the networks, which is readily possible due to the reversible formation of the supramolecular cross-links and their orthogonal stimuli-responsiveness.

摘要

双聚合物网络(DNs)由两个互穿的聚合物网络组成,其性能并非各部分性能的简单加和。在此,我们报道了一种由两种超分子聚合物(SMPs)制成的弹性DN,这两种聚合物由相同的聚(丙烯酸正丁酯)(BA)主链构成。这两种聚合物具有不同的非共价结合基序,可形成动态、可逆的交联。这些聚合物是通过丙烯酸正丁酯与自互补氢键基序2-脲基-4[1H]嘧啶酮或与金属离子形成配合物的2,6-双(1'-甲基苯并咪唑基)吡啶配体进行可逆加成-断裂链转移聚合制备而成。由这些组分制成的超分子DN结合了单个网络的特性,包括高热稳定性和抗蠕变性。该DN还具有出色的自愈性,并且比其组分表现出更高的拉伸性和韧性。通过选择性地预拉伸其中一个网络,DN的机械特性可以进一步增强,由于超分子交联的可逆形成及其正交刺激响应性,这很容易实现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37a1/11665491/3134ae4374fa/CHEM-30-e202402511-g002.jpg

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