ABSTRACT
Synthetic covalent monolayer sheets and their subclass, two-dimensional polymers are of particular interest in materials science because of their special dimensionality which renders them very different from any bulk matter. However, structural analysis of such entities is rather challenging, and there is a clear need for additional analytical methods. The present study shows how tip-enhanced Raman spectroscopy (TERS) can be performed on monomer monolayers and the covalent sheets prepared from them by [4 + 4]-cycloaddition to explore rather complex structural and mechanistic issues. TERS is a surface analytical method that combines the high lateral resolution of scanning probe microscopy (SPM) with a greatly enhanced Raman scattering intensity. The high spatial resolution (<60 nm) and the significantly improved sensitivity (contrast factor of >4000) compared to confocal Raman microscopy provides new insights into the formation of this new and exciting material, namely significant consumption of the reactive units (anthracenes) and exclusion of the alternative [4 + 2]-cycloaddition. Moreover, due to the high lateral resolution, it was possible to find a first spectroscopic hint for step growth as the dominant mechanism in the formation of these novel monolayer sheets. In addition, TERS was used to get first insights into the phase behavior of a comonomer mixture.
ABSTRACT
By using structurally similar amphiphilic monomers, it is shown that compressed monolayers of varying amounts of such monomers at the air/water interface can be converted by photo-irradiation into the corresponding covalently connected monolayer sheets. Since one of the monomers carries three anthracene units and the other three 1,8-diaza-anthracene units, the growth reaction is proposed to take place through photochemically achieved [4+4]-cycloaddition between pairs of these units that are co-facially (face-to-face) arranged, to furnish the corresponding covalent dimers. While evidence for both homodimers is amply available, the existence of the heterodimer needs to be established with the help of a model reaction to support the conceptual aspect of this work, copolymerization in two dimensions. The sheet copolymers exhibit substantial robustness in that they can be spanned over 20 × 20 µm(2)-sized holes without rupturing under their own weight. X-ray photoelectron spectroscopy (XPS) studies reveal that the monomers are incorporated into the sheet copolymers according to feed. These results establish existence of the first covalent sheet copolymer, which is considered a step ahead towards novel 2D materials.
