The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
The Halogen Bond in the Design of Functional Supramolecular Materials: Recent Advances
Open accessAbstract
Halogen bonding is an emerging noncovalent interaction for constructing supramolecular assemblies. Though similar to the more familiar hydrogen bonding, four primary differences between these two interactions make halogen bonding a unique tool for molecular recognition and the design of functional materials. First, halogen bonds tend to be much more directional than (single) hydrogen bonds. Second, the interaction strength scales with the polarizability of the bond-donor atom, a feature that researchers can tune through single-atom mutation. In addition, halogen bonds are hydrophobic whereas hydrogen bonds are hydrophilic. Lastly, the size of the bond-donor atom (halogen) is significantly larger than hydrogen. As a result, halogen bonding provides supramolecular chemists with design tools that cannot be easily met with other types of noncovalent interactions and opens up unprecedented possibilities in the design of smart functional materials. This Account highlights the recent advances in the design of halogen-bond-based functional materials. Each of the unique features of halogen bonding, directionality, tunable interaction strength, hydrophobicity, and large donor atom size, makes a difference. Taking advantage of the hydrophobicity, researchers have designed small-size ion transporters. The large halogen atom size provided a platform for constructing all-organic light-emitting crystals that efficiently generate triplet electrons and have a high phosphorescence quantum yield. The tunable interaction strengths provide tools for understanding light-induced macroscopic motions in photoresponsive azobenzene-containing polymers, and the directionality renders halogen bonding useful in the design on functional supramolecular liquid crystals and gel-phase materials. Although halogen bond based functional materials design is still in its infancy, we foresee a bright future for this field. We expect that materials designed based on halogen bonding could lead to applications in biomimetics, optics/photonics, functional surfaces, and photoswitchable supramolecules.
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Cites
Definition of the halogen bond (IUPAC Recommendations 2013).
Desiraju, G. R., Ho, P. S., Kloo, L., Legon, A. C., Marquardt, R., Metrangolo, P., Politzer, P., Resnati, G., & Rissanen, K. (2013) · Pure and Applied Chemistry · doi:10.1351/pac-rec-12-05-10 · Cited by 1,957
Self-citationActivating efficient phosphorescence from purely organic materials by crystal design
Bolton, O., Lee, K., Kim, H.-J., Lin, K. Y., & Kim, J. (2011) · Nature Chemistry · doi:10.1038/nchem.984 · Cited by 1,662
Crystallization-Induced Phosphorescence of Pure Organic Luminogens at Room Temperature
Yuan, W. Z., Shen, X. Y., Zhao, H., Lam, J. W. Y., Tang, L., Lu, P., Wang, C., Liu, Y., Wang, Z., Zheng, Q., et al. (2010) · The Journal of Physical Chemistry C · doi:10.1021/jp909388y · Cited by 989
Cited by
Krishna, G. R., Devarapalli, R., Lal, G., & Reddy, C. M. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b05118 · Cited by 365
Metadata
- Authors
- Priimagi, A., Cavallo, G., Metrangolo, P., & Resnati, G.
- Venue
- Accounts of Chemical Research
- Publisher
- American Chemical Society (ACS)
- Published
- 2013-06-27
- Volume
- 46
- Issue
- 11
- Pages
- 2686-2695
- ISSN
- 0001-4842 (ISSN-L)
- 1520-4898
- OpenAlex
- W2051828492
- Cited by
- 881
- References
- 3
- FWCI
- 52.99
- Type
- journal article
- Language
- en
- Open access
- hybrid
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