Micrometre-long covalent organic fibres by photoinitiated chain-growth radical polymerization on an alkali-halide surface

化学 聚合 聚合物 去湿 化学工程 单体 解吸 自由基聚合 纳米材料 高分子化学 光化学 纳米技术 薄膜 吸附 材料科学 有机化学 工程类
作者
Franck Para,François Bocquet,Laurent Nony,Christian Loppacher,Michel Féron,Frédéric Cherioux,David Z. Gao,Filippo Federici Canova,Matthew Watkins
出处
期刊:Nature Chemistry [Nature Portfolio]
卷期号:10 (11): 1112-1117 被引量:40
标识
DOI:10.1038/s41557-018-0120-x
摘要

On-surface polymerization is a promising technique to prepare organic functional nanomaterials that are challenging to synthesize in solution, but it is typically used on metal substrates, which play a catalytic role. Previous examples on insulating surfaces have involved intermediate self-assembled structures, which face high barriers to diffusion, or annealing to higher temperatures, which generally causes rapid dewetting and desorption of the monomers. Here we report the photoinitiated radical polymerization, initiated from a two-dimensional gas phase, of a dimaleimide monomer on an insulating KCl surface. Polymer fibres up to 1 μm long are formed through chain-like rather than step-like growth. Interactions between potassium cations and the dimaleimide’s oxygen atoms facilitate the propagation of the polymer fibres along a preferred axis of the substrate over long distances. Density functional theory calculations, non-contact atomic force microscopy imaging and manipulations at room temperature were used to explore the initiation and propagation processes, as well as the structure and stability of the resulting one-dimensional polymer fibres. On-surface polymerization is a promising technique to prepare organic functional nanomaterials, but it has remained difficult to carry out on insulating surfaces. Now, the photoinitiated radical polymerization of dimaleimide on KCl, initiated from a two-dimensional gas phase and guided by molecule–substrate interactions, has led to polymer fibres up to 1 μm long.

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