The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.
Halogen Bonding Based Recognition Processes: A World Parallel to Hydrogen Bonding
Abstract
Halogen bonding is the noncovalent interaction between halogen atoms (Lewis acids) and neutral or anionic Lewis bases. The main features of the interaction are given, and the close similarity with the hydrogen bonding will become apparent. Some heuristic principles are presented to develop a rational crystal engineering based on halogen bonding. The focus is on halogen-bonded supramolecular architectures given by halocarbons. The potential of the interaction is shown by useful applications in the field of synthetic chemistry, material science, and bioorganic chemistry.
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Citations
Cites
van der Waals Volumes and Radii
Bondi, A. (1964) · The Journal of Physical Chemistry · doi:10.1021/j100785a001 · Cited by 19,350
Halogen bonds in biological molecules
Auffinger, P., Hays, F. A., Westhof, E., & Ho, P. S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407607101 · Cited by 1,634
Halogen Bonding: A Paradigm in Supramolecular Chemistry
Metrangolo, P., & Resnati, G. (2001) · Chemistry - A European Journal · doi:10.1002/1521-3765(20010618)7:12<2511::aid-chem25110>3.0.co;2-t · Cited by 1,008
Self-citationThe Nature and Geometry of Intermolecular Interactions between Halogens and Oxygen or Nitrogen
Lommerse, J. P. M., Stone, A. J., Taylor, R., & Allen, F. H. (1996) · Journal of the American Chemical Society · doi:10.1021/ja953281x · Cited by 806
Structural Aspects of Interatomic Charge-Transfer Bonding
Hassel, O. (1970) · Science · doi:10.1126/science.170.3957.497 · Cited by 470
Santis, A. D., Forni, A., Liantonio, R., Metrangolo, P., Pilati, T., & Resnati, G. (2003) · Chemistry - A European Journal · doi:10.1002/chem.200204655 · Cited by 143
Self-citationMessina, M. T., Metrangolo, P., Panzeri, W., Pilati, T., & Resnati, G. (2001) · Tetrahedron · doi:10.1016/s0040-4020(01)00794-3 · Cited by 123
Self-citationCardillo, P., Corradi, E., Lunghi, A., Meille, S. V., Messina, M. T., Metrangolo, P., & Resnati, G. (2000) · Tetrahedron · doi:10.1016/s0040-4020(00)00476-2 · Cited by 105
Self-citationBertani, R., Metrangolo, P., Moiana, A., Pérez, E., Pilati, T., Resnati, G., Rico‐Lattes, I., & Sassi, A. (2002) · Advanced Materials · Cited by 94
Self-citationCrystal Structures of Two Potent Nonamidine Inhibitors Bound to Factor Xa ,
Adler, M., Kochanny, M. J., Ye, B., Rumennik, G., Light, D. R., Biancalana, S., & Whitlow, M. D. (2002) · Biochemistry · doi:10.1021/bi0264061 · Cited by 93
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Clark, T., Hennemann, M., Murray, J. S., & Politzer, P. (2007) · Journal of Molecular Modeling · doi:10.1007/s00894-006-0130-2 · Cited by 2,314
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Bissantz, C., Kuhn, B., & Stahl, M. (2010) · Journal of Medicinal Chemistry · doi:10.1021/jm100112j · Cited by 1,731
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Desiraju, G. R. (2013) · Journal of the American Chemical Society · doi:10.1021/ja403264c · Cited by 1,517
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Hernandes, M., Cavalcanti, S. M., Moreira, D. R., de Azevedo Junior, W., & Leite, A. C. (2010) · Current Drug Targets · doi:10.2174/138945010790711996 · Cited by 723
The Bright Future of Unconventional σ/π‐Hole Interactions
Bauzá, A., Mooibroek, T. J., & Frontera, A. (2015) · ChemPhysChem · doi:10.1002/cphc.201500314 · Cited by 710
σ-Hole Bond vs π-Hole Bond: A Comparison Based on Halogen Bond
Wang, H., Wang, W., & Jin, W. J. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00527 · Cited by 631
Halogen Bonding—A Novel Interaction for Rational Drug Design?
Lu, Y., Shi, T., Wang, Y., Yang, H., Yan, X., Luo, X., Jiang, H., & Zhu, W. (2009) · Journal of Medicinal Chemistry · doi:10.1021/jm9000133 · Cited by 559
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Biedermann, F., & Schneider, H.-J. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00583 · Cited by 554
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Kozuch, S., & Martin, J. M. L. (2013) · Journal of Chemical Theory and Computation · doi:10.1021/ct301064t · Cited by 553
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Mahmudov, K. T., Kopylovich, M. N., Guedes da Silva, M. F. C., & Pombeiro, A. J. L. (2017) · Dalton Transactions · doi:10.1039/c7dt01685a · Cited by 466
Halogen bonding (X‐bonding): A biological perspective
Scholfield, M. R., Zanden, C. M. V., Carter, M., & Ho, P. S. (2013) · Protein Science · doi:10.1002/pro.2201 · Cited by 451
Halogen Bond: Its Role beyond Drug–Target Binding Affinity for Drug Discovery and Development
Xu, Z., Yang, Z., Liu, Y., Lu, Y., Chen, K., & Zhu, W. (2014) · Journal of Chemical Information and Modeling · doi:10.1021/ci400539q · Cited by 431
Riley, K. E., & Hobza, P. (2008) · Journal of Chemical Theory and Computation · doi:10.1021/ct700216w · Cited by 428
Riley, K. E., Murray, J. S., Fanfrlík, J., Řezáč, J., Solá, R. J., Concha, M. C., Ramos, F. M., & Politzer, P. (2011) · Journal of Molecular Modeling · doi:10.1007/s00894-011-1015-6 · Cited by 405
Halogen bonding in metal–organic–supramolecular networks
Bertani, R., Sgarbossa, P., Venzo, A., Lelj, F., Amati, M., Resnati, G., Pilati, T., Metrangolo, P., & Terraneo, G. (2010) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2009.09.035 · Cited by 364
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Hartlieb, K. J., Holcroft, J. M., Moghadam, P. Z., Vermeulen, N. A., Algaradah, M. M., Nassar, M. S., Botros, Y. Y., Snurr, R. Q., & Stoddart, J. F. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.5b12860 · Cited by 323
Riley, K. E., Murray, J. S., Politzer, P., Concha, M. C., & Hobza, P. (2009) · Journal of Chemical Theory and Computation · doi:10.1021/ct8004134 · Cited by 318
Chudzinski, M. G., McClary, C. A., & Taylor, M. S. (2011) · Journal of the American Chemical Society · doi:10.1021/ja202096f · Cited by 293
Berger, G., Soubhye, J., & Meyer, F. (2015) · Polymer Chemistry · doi:10.1039/c5py00354g · Cited by 260
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Yang, Z., Liu, Y., Chen, Z., Xu, Z., Shi, J., Chen, K., & Zhu, W. (2015) · Journal of Molecular Modeling · doi:10.1007/s00894-015-2681-6 · Cited by 23
Metadata
- Authors
- Metrangolo, P., Neukirch, H., Pilati, T., & Resnati, G.
- Venue
- Accounts of Chemical Research
- Publisher
- American Chemical Society (ACS)
- Published
- 2005-03-17
- Volume
- 38
- Issue
- 5
- Pages
- 386-395
- ISSN
- 0001-4842 (ISSN-L)
- 1520-4898
- OpenAlex
- W2131214655
- Cited by
- 1,915
- References
- 17
- FWCI
- 45.84
- Type
- journal article
- Language
- en
- Open access
- closed
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