Similar to hydrogen bonding supramolecular diblock polymers, these formations were also highly solvent dependent. Further developments to these systems revealed that well‐defined inverted vesicle morphologies could be facilitated by the hydrophobicity of the halogen bond [185].
Triblock terpolymers are another class of polymer that can form microparticles with more functional domains than diblock polymers. However, strategies to predict how triblock terpolymers assemble are in their infancy. Quintieri et al. first developed ABC 3D styrene‐based triblock terpolymers utilizing the halogen bond [186]. In this study, a variety of hydroxy hydrogen bond and perfluoroiodobenzene halogen bond donors were used to form microparticles under confinement (Figure 1.20a). Interestingly, the particles formed either lamella–sphere or lamella–lamella morphologies based on the type of donor (Figure 1.20b). In general, weaker hydrogen or halogen donors lead to increased particle volume. Therefore, they found that both the donor strength and intermolecular packing interactions were important for the overall morphology of the nanoparticle.
1.5.3.4 Self‐healing Polymers
Select self‐healing polymers employ reversible networks of noncovalent interactions and are of topical interest for several real‐world applications. For example, using halogen bonds in self‐healing polymers allows for the creation of hard coatings with healing properties. The polymers are “repaired” by reorganizing noncovalent interactions to maintain structural and mechanical integrity and can sustain many healing cycles while keeping their mechanical robustness. The first examples of halogen bond self‐healing polymers were developed by Schubert and Hager in 2017 [187,188]. Cross‐linking between iodotriazole and iodotriazolium halogen bond donors and tetra‐N‐butylammonium acetate polymeric salt acceptors (Figure 1.21) in these systems was revealed by a characteristic shift in the C–I band in the Raman spectrum. The self‐healing behavior in these polymers was indicated by scratch‐healing tests. Future studies of self‐healing polymers that incorporate halogen bonding are being directed at maximizing the self‐healing mechanism. Given that there are few examples, the field will likely expand to include a wider variety of self‐healing polymer systems.
1.5.4 Supramolecular Gels
Low molecular weight supramolecular gels can be used for sensing, cell growth media, drug delivery, and stimuli‐responsive optical/electronic materials. Hydrogen bond interactions are commonly used to form 1D or 2D fibrils that are sensitive to competing noncovalent interactions. These competing interactions can therefore be used to control gel formation or gel strength. Metrangolo and Resnati created 1,4‐diiodotetrafluorobenzene and 1,4‐bis(3‐pyridylureido)butane mixtures whose crystal structure revealed a halogen bonding diiodoperfluorobenzene donor, pyridine acceptor, and hydrogen bonding urea donor–acceptor lattice. This combination of molecules resulted in the formation of a supramolecular polymeric gel in dimethyl sulfoxide–water mixtures [189]. This was the first example using a halogen bond to form a supramolecular gel in polar media, suggesting that halogen bonds can operate in the presence of polar solvents and be used for gel‐based materials [190]. The linearity of the halogen bond has also been exploited to develop macroscale materials [191]. By using a halogen bonding 1‐iodoperfluoroalkane donor with a polyethylene glycol‐based ammonium chloride end‐capped acceptor, a star‐shaped polymer was created, which formed millimeter‐sized films without any other external templating forces. Even in the few reported systems, the halogen bond has been versatile enough to produce polymeric gels in competitive media and strong enough to generate millimeter scale assemblies.
Figure 1.20 (a) Chemical structure of the halogen bond and hydrogen bond donors used in nanoparticle formation. (b) Tuning of the poly(4‐vinylpyridine) (P4VP) volume with halogen bond and hydrogen bond donors and transition from lamella–sphere to lamella–lamella morphology.
Source: From Quintieri et al. [186]. © 2018 MDPI.
Figure 1.21 Monomers M1 and M2 were subjected to RAFT polymerization with butyl methacrylate (BMA) to prepare the donor‐containing copolymers P1 and P2, which were methylated to obtain P3 and P4. Acceptor copolymers P5 and P6 were obtained by RAFT polymerization of BMA with methyl methacrylate (MAA) and subsequent treatment with TBAOH.
Source: From Tepper et al. [187]. © 2017 John Wiley & Sons
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1.5.5 Materials Conclusion
Despite the early stage of development, materials scientists have used the halogen bond to construct a diverse range of LCs, ionic liquids, self‐healing polymers, and macroscopic self‐assembled gels. These initial materials provide perspective for the detailed discussions of solution‐based halogen bonding found in subsequent chapters. However, halogen bond‐based materials are still largely inspired and derived from hydrogen bond‐based materials. Surely, combining the ingenuity of the chemist with the directionality, tunability, solvent resistance, and lipophilicity of the halogen bond will produce unique materials for a variety of exciting applications. Future studies will improve the properties of halogen bonding materials and will be used to gain a greater understanding of the noncovalent interactions available to the chemist.
1.6 Conclusion
From intellectual curiosity to versatile supramolecular tool, the ascension of the halogen bond has been significant. In less than 20 years since the “rediscovery” concept article, the works of many scientists have produced a solid foundational understanding of the halogen bond. The wide breadth of fundamental studies of the halogen bond across all phases (solid, solution, gas, and in silico) has resulted in extensive (and growing) application across diverse fields. Furthermore, the success of the halogen bond has inspired a renaissance of other σ‐hole‐type interactions (e.g. chalcogen, pnictogen, and tetrel bonds) that have developed rapidly, as concepts, nomenclature, and fundamentals parallel the halogen bond.
The rise of these noncovalent forces has expanded the supramolecular landscape. As such, readers should continue to expect comparative investigations on how the halogen bond “stacks up” against other noncovalent interactions – some of which will be discussed in later chapters. These and other fundamental studies will continue to refine our understanding of the halogen bond. As the field advances, enriched understanding and computational models will lead to improved molecular designs – the prospects of which are vast. The intent of this introduction has been to provide a deeper understanding of the halogen bond that can be used to contextualize the solution discussions found in later chapters. The following chapters highlight fundamental and functional studies of the halogen bond in solution.
Acknowledgments
O.B.B., D.A.D., and E.A.J. are