Crosslinking of poly(n-butyl acrylate)-POSS copolymers via dynamic urea exchange enables self-healing, reprocessing and shape recovery. Issue 7 (27th January 2023)

• Record Type: Journal Article
• Authors: Wang, Huaming; Hang, Guohua; Mei, Honggang; Li, Lei; Zheng, Sixun
• Is Part Of: Polymer chemistry. Volume 14:Issue 7(2023)
• Page Start: 872
• Page End: 887
• Publication Date: 2023-01-27
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/d2py01414a
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : In this contribution, we reported a novel approach to crosslink linear poly( n -butyl acrylate)-POSS copolymers via a dynamic urea exchange reaction. Abstract : In this contribution, we reported a novel approach to crosslink linear poly( n -butyl acrylate)-POSS copolymers via a dynamic urea exchange reaction. First, the linear copolymers of n -butyl acrylate, POSS acrylate and 2-(3-( tert -butyl)-3-methylureido)ethylacrylate were synthesized via radical reversible addition–fragmentation chain transfer (RAFT) polymerization. Of these copolymerization monomers, 2-(3-( tert -butyl)-3-methylureido)ethylacrylate was synthesized by the reaction of 2-isocyanatoethyl acrylate with N-tert -butylmethylamine ( i.e., a hindered monoamine); it carries a single hindered urea bond (HUB). Owing to the introduction of 2-(3-( tert -butyl)-3-methylureido)ethylacrylate structural units, the linear copolymers can be further crosslinked with 1, 2-bis( tert -butyl)ethylenediamine ( viz. a hindered diamine) via a dynamic urea exchange reaction. In the dynamic urea exchange reaction, every two 2-(3-( tert -butyl)-3-methylureido)ethylacrylate structural units reacted with one 1, 2-bis( tert -butyl)ethylenediamine, generating one chemical linkage bearing two HUBs. The crosslinking of the linear copolymers with HUBs enabled the self-healing and/or reprocessing of the organic–inorganic networks. In addition, the organic–inorganic nanocomposites displayed excellent thermally-induced shape memory properties due to the generation of networks. Furthermore, the original shapes of the shape memory polymers can be re-edited by utilizing the dynamic exchange of HUBs.