Nikita Orekhovad,
Nina Bukhtiiarovaab,
Zlata A. Brushevicha,
Anton A. Muraveva,
Elad Nadavc,
Yael Tsarfatib,
Anna Kossoyc,
Isai Feldmanc,
Anastasia Zeleninad,
Anna A. Rubekinae,
Sergey N. Semenov
*b and
Ekaterina V. Skorb
*a
aInfochemistry Scientific Center, ITMO University, Saint Petersburg, Russia. E-mail: skorb@itmo.ru
bDepartment of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot, Israel. E-mail: sergey.semenov@weizmann.ac.il
cDepartment of Chemical Research Support, Weizmann Institute of Science, Rehovot, Israel
dMoscow Center for Advanced Studies, Moscow, Russia
eLomonosov Moscow State University, Moscow, Russia
First published on 14th August 2024
Herein, we obtained two supramolecular assemblies with layered structures from melamine, N-methylmelamine, and hexynyl-cyanuric acid in water. By combination of X-ray diffraction, electron microscopy, and molecular dynamics studies, we found that introducing one methyl group in melamine alters the arrangement of the layers in these structures.
Here, we characterized two 3D supramolecular structures formed from hexynyl-cyanuric acid (HCA) and melamine (M) or N-methyl melamine (MM) by combining high-resolution transmission electron microscopy (TEM), powder X-ray diffraction (XRD), and molecular dynamics (MD) simulations. Interestingly, the small change in molecular building blocks originating from methyl substituents in the melamine altered the final structures.
We used HCA, M, and MM as building blocks for the supramolecular structures in this study (Fig. 1). HCA was chosen for two reasons: (i) it can form two triple hydrogen bonds at 120°, and therefore, it can participate in rosette and tape motifs; (ii) its alkyne group can facilitate further surface modification of the materials by the azide–alkyne click reaction. M and MM were chosen because they are the simplest complementary blocks for HCA. However, methylation introduces an important difference into the properties of these molecules: if M can form 3 strong triple hydrogens, MM can form only 2 strong hydrogen bonds, and a third bond will be disrupted by the methyl group.
![]() | ||
Fig. 1 Layered structures formed by self-assembly of hexynil cyanuric acid with (a) melamine and (b) N-methylmelamine. |
We synthetized HCA by reacting the mesylate of hex-5-yn-1-ol with cyanuric acid in the presence of DBU.23 The supramolecular materials (Fig. 1) were initially obtained by mixing equimolar amounts of aqueous solutions of HCA (10 mM) and M (10 mM) or MM (10 mM) and then filtering the formed precipitates. Experimentally, the acceptable range of the concentrations of the reacting solutions is from 1–10 mM. At lower concentrations, a precipitate did not form, and higher concentrations are not accessible because of the solubility of HCA. The materials formed in this way have low crystallinity according to powder XRD (Fig. S1, ESI†). More crystalline materials, which were used for structural studies, were obtained by mixing solutions at 80 °C (when precipitation does not occur) and slowly cooling the mixture in a Dewar flask.
The materials obtained by slow cooling showed well-defined XRD patterns (Fig. 2a and b). These patterns pointed towards layered structures; the first peaks can be attributed to a series with 23.85 and 28.36 Å spacing for the M*HCA and MM*HCA structures, correspondingly. From the geometrical considerations, a distance of 28 Å roughly corresponds to the doubled thickness of M*HCA H-bonded tape (∼14 Å), whereas a distance of 24 Å might correspond to two M*HCA tapes with intertwined hexynyl tails (Fig. 2c and d). For M*HCA the first peak in the series (d = 23.85 Å) is strong, but for MM*HCA the second peak in the series (d = 14.18 Å) is the strongest; however, the first peak (d = 28.36 Å) is very weak. This relationship between the first and second peaks in the series was retained in patterns obtained from samples in capillaries (Fig. S2, ESI†) and in measurements with transmission instead of reflection geometry (Fig. S3, ESI†); therefore, the effects due to the preferable orientation of the crystallites were eliminated. In addition, scanning electron microscopy images of the samples used for XRD revealed no preferable orientation of microcrystals (Fig. S4–S8, ESI†), but instead, a sponge-like morphology with no preferential direction. These observations indicate the existence of destructive interference for the reflection corresponding to the first peak in MM*HCA, which would be expected for the arrangement shown in Fig. 2d. In addition, both XRD patterns have strong peaks at around 3.3 Å (3.31 Å for M*HCA and 3.36 Å for MM*HCA), which is typical for π–π stacked layers in melamine cyanurate.24 Nevertheless, the quality of the XRDs was insufficient for complete indexing and structural determination. Therefore, we decided to use it in combination with high-resolution TEM and MD simulations to confirm the major structural motifs in these materials.
![]() | ||
Fig. 2 XRD patterns of M*HCA (a) and MM*HCA (b) as well as estimation of characteristic periods for tail-to-tail (c) and head-to-tail (d) arrangements. |
In the TEM studies, we used two protocols for sample preparation: with and without cryo-drying. The best results for M*HCA were obtained without cryo-drying. The images showed flat crystallites with a layered structure (Fig. 3a, see also Fig. S9 and S10, ESI†). The side view of a crystallite clearly showed layers with spacing of about 23.9 Å, which is in excellent correspondence with XRD. The top view of a crystallite showed a spacing of 3.3 Å, again an excellent correspondence with XRD. All together, TEM resembled the structure shown in Fig. 1, with double-layers of M*HCA in which the hexynyl tails point towards each other.
For MM*HCA, the quality of the TEM images was generally lower than that of M*HCA. Nevertheless, the image capturing the side view of a crystallite (Fig. 3b) showed a spacing of 14.5 Å, which is a good agreement with 14.03 Å for the strongest reflection in XRD. FFT analysis of the top view of the crystallite (Fig. 3c) revealed a spacing of 3.7 Å, which is in reasonable agreement with 3.4 Å observed in XRD. Overall, the XRD and TEM studies pointed towards layered structure shown in Fig. 1.
To further confirm the proposed structures of M*HCA and MM*HCA, we constructed their models using MD (Fig. 4a and b).25,26 The models confirmed the periodicity observed in XRD and TEM as well as gave a good agreement between experimental and calculated XRD patterns (Fig. 4c and d). To better understand the differences between the two structures, we compared the potential energies of interatomic interactions per pair of molecules E for the tail-to-tail and head-to-tail arrangements of layers made of M*HCA and MM*HCA (Fig. 4e). The figure shows that the M*HCA tail-to-tail arrangement is favored over the head-to-tail arrangement by about 10 kcal mol−1. For MM*HCA, these two arrangements are energetically approximately equivalent. Thus, for M*HCA, one of the reasons for its tail-to-tail arrangement is its higher thermodynamic stability, compared with the head-to-tail arrangement. However, during the growth of these structures, the kinetic factors are more likely to define the final arrangements than are the thermodynamic factors. Therefore, we performed two 500 ns-long MD simulations of M*HCA and MM*HCA surface growth from the water solution. For M*HCA crystal, we observe the orientation of molecules in newly formed layers resulting in the tail-to-tail arrangement that facilitates M–M hydrogen bonding (Fig. S11a, ESI†), while for MM*HCA these layers are more amorphous (Fig. S11b, ESI†). This amorphous nature can be attributed to the shorter timescale of MD simulations in comparison with real experiments, which does not provide enough time for molecules to arrange properly.
In summary, we characterized two layered supramolecular structures assembled in water from melamine and cyanuric acid derivatives. The layers in both structure consist of H-bonded tapes stacked by π–π interactions. Interestingly, these layers are arranged differently for the assemblies, differing by only one methyl group in the melamine component. M forms the structure with a tail-to tail arrangement and the bilayer is the major repeating motif, whereas MM forms the structure with a head-to tail arrangement and the monolayer is the major repeating motif. The balance between H-bonding and van der Waals interactions likely plays a critical role in this difference.3,15 M favors H-bonding, an interaction that holds bilayers in the tail-to tail arrangement; however, the methyl group hampers these interactions for the MM-based assembly to the extent where they become comparable to the van der Waals interactions between MM and hexynyl tails of HCA. In the context of supramolecular chemistry, this work highlights the fact that water is a unique solvent in which the balance between all types of non-covalent interactions is important in defining the final structure. Therefore, highly ordered structures can be obtained from very simple building blocks such as M, MM, and HCA in water. In the context of materials science, the reversibility of the assembly-disassembly of these structures upon heating in water and in the presence of the “clickable” alkyne groups opens the possibility to use these compounds as scaffolds for dynamic functional materials.
S. N. S. and E. V. S. supervised the research. S. N. S., E. V. S., N. O. and N. B. designed experiments. N. B., Z. A. B, and A. A. M. synthesized starting materials. N. B. synthesized M*HCA and MM*HCA. N. O., A. Z. and A. A. R. performed MD simulations. N. E. and Y. T. performed and analyzed TEM measurements. A. K. performed and analyzed SEM measurements. I.F. performed and analyzed XRD measurements. E. V. S., N. O., A. Z. and S. N. S. wrote the manuscript.
Authors thank Alexandr Mityaev and Alexander Tsirlin for helpful discussions. Authors acknowledge RSF grant no. 24-13-00355 for the support. We thank Priority 2030 for infrastructural support. A. A. R. acknowledges support from the Fund of Theoretical Physics and Mathematics Development “BASIS” No. 20-2-10-6-1.
Footnote |
† Electronic supplementary information (ESI) available: Synthetic, analytical, and computational protocols, Fig. S1–S11. See DOI: https://doi.org/10.1039/d4cc02817a |
This journal is © The Royal Society of Chemistry 2024 |