Definition of the halogen bond (IUPAC Recommendations 2013).

Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)

Müller, P. (1994) · Pure and Applied Chemistry · doi:10.1351/pac199466051077 · Cited by 1,606

Glossary of terms used in theoretical organic chemistry

Minkin, V. I. (1999) · Pure and Applied Chemistry · doi:10.1351/pac199971101919 · Cited by 436

Key-to-lock halogen bond-based tetragonal pyramidal association of iodonium cations with the lacune rims of beta-octamolybdate

Soldatova, N. S., Radzhabov, A. D., Ivanov, D. M., Burguera, S., Frontera, A., Abramov⧫, P. A., Постников, П. С., & Kukushkin, V. Y. (2024) · Chemical Science · doi:10.1039/d4sc01695e · Cited by 16

Inclusion complexes of C ethyl -2-methylresorcinarene and pyridine N -oxides: breaking the C–I⋯ − O–N + halogen bond by host–guest complexation

Puttreddy, R., Beyeh, N. K., & Rissanen, K. T. (2015) · CrystEngComm · doi:10.1039/c5ce02354h · Cited by 16

Viscosity measurements of R32 and R410A to 350 MPa

Bair, S. S., & Laesecke, A. (2017) · International Journal of Refrigeration · doi:10.1016/j.ijrefrig.2017.07.016 · Cited by 16

Halogen Bonding Involving CO and CS with Carbon as the Electron Donor

Bene, J. E. D., Alkorta, I., & Elguero, J. (2017) · Molecules · doi:10.3390/molecules22111955 · Cited by 16

Probing non-covalent interactions driving molecular assembly in organo-electronic building blocks

Johnson, S. N., Ellington, T. L., Ngo, D. T., Nevarez, J. L., Sparks, N. E., Rheingold, A. L., Watkins, D. L., & Tschumper, G. S. (2019) · CrystEngComm · doi:10.1039/c9ce00219g · Cited by 16

Energy Decomposition Analysis for Interactions of Radicals: Theory and Implementation at the MP2 Level with Application to Hydration of Halogenated Benzene Cations and Complexes between CO2–· and Pyridine and Imidazole

Loipersberger, M., Lee, J., Mao, Y., Das, A. K., Ikeda, K., Thirman, J., Head-Gordon, T. L., & Head‐Gordon, M. (2019) · The Journal of Physical Chemistry A · doi:10.1021/acs.jpca.9b08586 · Cited by 15

Delocalized relativistic effects, from the viewpoint of halogen bonding

Sarr, S., Graton, J., Rahali, S., Montavon, G., & Galland, N. (2020) · Physical Chemistry Chemical Physics · doi:10.1039/d0cp05840h · Cited by 16

Strength of the [Z–I···Hal]− and [Z–Hal···I]− Halogen Bonds: Electron Density Properties and Halogen Bond Length as Estimators of Interaction Energy

Kuznetsov, M. L. (2021) · Molecules · doi:10.3390/molecules26072083 · Cited by 16

Halogen Bond Catalyzed Bromocarbocyclization

Chan, Y., & Yeung, Y. (2018) · Angewandte Chemie · doi:10.1002/ange.201800261 · Cited by 16

Chalcogen-bonded complexes of some carbon dioxide analogues

Ramasami, P., & Ford, T. A. (2014) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2014.03.055 · Cited by 16

Role of halogen-involved intermolecular interactions and existence of isostructurality in the crystal packing of —CF3 and halogen (Cl or Br or I) substituted benzamides

Mondal, P. K., Shukla, R., Biswas, S., & Chopra, D. (2018) · Acta Crystallographica Section B Structural Science Crystal Engineering and Materials · doi:10.1107/s2052520618013422 · Cited by 16

Phenomenal Observation of Attractive Intermolecular CH⋯HC Interaction in a Mercury (II) Complex: An Experimental and First‐Principles Study

Khavasi, H. R., Balmohammadi, Y., & Naghavi, S. S. (2019) · ChemistrySelect · doi:10.1002/slct.201901932 · Cited by 16

Bi- and Trifurcated Halogen Bonding M–C≡N···I in 1D, 2D, and 3D Supramolecular Network Structures of Co-Crystallized Diiodoacetylene C2I2 and Tetracyanonickelate [Ni(CN)4]2–

Sellin, M., Rupf, S. M., Zhang, Y., & Malischewski, M. (2020) · Crystal Growth & Design · doi:10.1021/acs.cgd.0c01208 · Cited by 16

Effect of N-methyl and ethyl on phosphorescence of carbazole in cocrystals assembled by C I⋯π halogen bond, π-hole⋯π bond and other interactions using 1,4-diiodotetrafluorobenzene as donor

Zhu, Q., Gao, Y. J., Gao, H. Y., & Jin, W. J. (2014) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/j.jphotochem.2014.05.010 · Cited by 16

Highly Enantioselective Organocatalysis with Bidentate Halogen Bond Donors

Wolf, J., Mohanan, M. P., Robidas, R., Sutar, R. L., Engelage, E., Legault, C. Y., & Huber, S. M. (2025) · Angewandte Chemie International Edition · doi:10.1002/anie.202506476 · Cited by 15

The Next Frontier in the Study of Noncovalent Bonding: Transition Metals

Scheiner, S. (2025) · Molecules · doi:10.3390/molecules30173643 · Cited by 15

Charge‐Assisted Halogen Bonding in an Ionic Cavity of a Coordination Cage Based on a Copper(I) Iodide Cluster

Peuronen, A., Taponen, A. I., Kalenius, E., Lehtonen, A., & Lahtinen, M. (2022) · Angewandte Chemie International Edition · doi:10.1002/anie.202215689 · Cited by 15

Benzothienoiodolium Cations Doubly Bonded to Anions via Halogen–Chalcogen and Halogen–Hydrogen Supramolecular Synthons

Fedorova, I. I., Soldatova, N. S., Ivanov, D. M., Nikiforova, K., Aliyarova, I. S., Yusubov, M. S., Tolstoy, P. M., Gomila, R. M., Frontera, A., Kukushkin, V. Y., et al. (2023) · Crystal Growth & Design · doi:10.1021/acs.cgd.2c01485 · Cited by 15

A Review on Low‐Molecular‐Weight Gels Driven by Halogen‐Effect

Zhang, Y., Wang, J., Liao, Y., & Xie, X. (2023) · Chemistry - An Asian Journal · doi:10.1002/asia.202300097 · Cited by 15

Unified classification of non-covalent bonds formed by main group elements: a bridge to chemical bonding

Das, A., & Arunan, E. (2023) · Physical Chemistry Chemical Physics · doi:10.1039/d3cp00370a · Cited by 15

Halogen Bonding and/or Covalent Bond: Analogy of 3c–4e N···I···X (X = Cl, Br, I, and N) Interactions in Neutral, Cationic, and Anionic Complexes

Adeniyi, E. O., Odubo, F. E., Zeller, M., Torubaev, Y. V., & Rosokha, S. V. (2023) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.3c02843 · Cited by 15

Wolfium bonds in homodimers of MX 4 Y (M = Mo, W; X = F, Cl, Br; Y = O, S, Se)

Michalczyk, M., Zierkiewicz, W., & Scheiner, S. (2024) · Physical Chemistry Chemical Physics · doi:10.1039/d3cp05867k · Cited by 15

Luminescent sensors based on Ln(III) 2,5-diiodoterephthalate coordination polymers

Zaguzin, А. S., Abramov⧫, P. A., Рахманова, М. И., Usoltsev, A. N., Sokolov⧫, M. N., Петрович, Ф. В., & Adonin, S. A. (2024) · Polyhedron · doi:10.1016/j.poly.2024.116908 · Cited by 15

The Occurrence, Distribution, Environmental Effects, and Interactions of Microplastics and Antibiotics in the Aquatic Environment of China

Guo, Y., Shao, W., Zhao, W., & Zhu, H. (2024) · Water · doi:10.3390/w16101435 · Cited by 15

Molecular dynamics simulation of halogen bonding mimics experimental data for cathepsin L inhibition

Celis‐Barros, C., Saavedra-Rivas, L., Salgado, J. C., Cassels, B. K., & Zapata‐Torres, G. (2014) · Journal of Computer-Aided Molecular Design · doi:10.1007/s10822-014-9802-7 · Cited by 15

Observation of strong halogen bonds in the solid state structures of bis-haloimidazolium macrocycles

White, N. G., Caballero, A., & Beer, P. D. (2013) · CrystEngComm · doi:10.1039/c3ce41944d · Cited by 15

Role of Weak Hydrogen Bonds and Halogen Bonds in 5-Halo-1,3-dimethyluracils and Their Cocrystals—A Combined Experimental and Computational Study

Portalone, G., Moilanen, J. O., Tuononen, H. M., & Rissanen, K. T. (2016) · Crystal Growth & Design · doi:10.1021/acs.cgd.5b01727 · Cited by 15

S⋯N chalcogen bonded complexes of carbon disulfide with diazines. Theoretical study

Zierkiewicz, W., Fanfrlík, J., Michalczyk, M., Michalska, D., & Hobza, P. (2017) · Chemical Physics · doi:10.1016/j.chemphys.2017.11.014 · Cited by 15

Structural diversity in the products formed by the reactions of 2-arylselanyl pyridine derivatives and dihalogens

Montis, R., Arca, M., Aragoni, M. C., Blake, A. J., Castellano, C., Demartin, F., Isaia, F., Lippolis, V., Pintus, A., Lenardao, E. J., et al. (2018) · New Journal of Chemistry · doi:10.1039/c8nj00495a · Cited by 15

Characterization of electronic features of intermolecular interactions involving organic fluorine: Inputs from in situ cryo-crystallization studies on F and CF3 substituted anilines

Mondal, P. K., Hathwar, V. R., & Chopra, D. (2018) · Journal of Fluorine Chemistry · doi:10.1016/j.jfluchem.2018.03.016 · Cited by 15

Halogen bonding and triiodide asymmetry in cocrystals of triphenylmethylphosphonium triiodide with organoiodines

Kobra, K., O’Donnell, S., Ferrari, A., McMillen, C. D., & Pennington, W. T. (2018) · New Journal of Chemistry · doi:10.1039/c8nj01373j · Cited by 15

Polymeric Lead(II) Iodoacetate: Pb···I and I···I Non‐Covalent Interactions in the Solid State

Adonin, S. A., Novikov, A. S., & Sokolov⧫, M. N. (2019) · European Journal of Inorganic Chemistry · doi:10.1002/ejic.201900349 · Cited by 15

Interplay of Intra- and Intermolecular Interactions in Solid Iodine at Low Temperatures: Experimental and Theoretic Spectroscopy Study

Юшина, И. Д., & Kolesov, B. A. (2019) · The Journal of Physical Chemistry A · doi:10.1021/acs.jpca.9b01167 · Cited by 15

Reactions Catalyzed by 2-Halogenated Azolium Salts: From Halogen-Bond Donors to Brønsted-Acidic Salts

Kobayashi, Y., & Takemoto, Y. (2020) · Synlett · doi:10.1055/s-0039-1690815 · Cited by 15

The σ-hole⋯σ-hole stacking interaction: An unrecognized type of noncovalent interaction

Zhang, Y., & Wang, W. (2020) · The Journal of Chemical Physics · doi:10.1063/5.0033470 · Cited by 15

Tuning of Ionic Liquid Crystal Properties by Combining Halogen Bonding and Fluorous Effect

Cavallo, G., Abate, A., Rosati, M., Venuti, G. P., Pilati, T., Terraneo, G., Resnati, G., & Metrangolo, P. (2021) · ChemPlusChem · doi:10.1002/cplu.202100046 · Cited by 15

Nature of the Hydrogen Bond Enhanced Halogen Bond

Portela, S., & Fernández, I. (2021) · Molecules · doi:10.3390/molecules26071885 · Cited by 15

Chiral Ferrocenyl−Iodotriazoles and −Iodotriazoliums as Halogen Bond Donors. Synthesis, Solid State Analysis and Catalytic Properties.

Aubert, E., Doudouh, A., Wenger, E., Sechi, B., Peluso, P., Pale, P., & Mamane, V. (2022) · European Journal of Inorganic Chemistry · doi:10.1002/ejic.202100927 · Cited by 15

Can We Merge the Weak and Strong Tetrel Bonds? Electronic Features of Tetrahedral Molecules Interacted with Halide Anions

Bartashevich, E. V., Mukhitdinova, S. E., Klyuev, I. V., & Григорьевич, Ц. В. (2022) · Molecules · doi:10.3390/molecules27175411 · Cited by 15

The addition of halogens and interhalogens on palladacyclopentadienyl complexes bearing quinolyl-thioether as spectator ligands. A kinetic and computational study

Canovese, L., Visentin, F., Scattolin, T., Santo, C. I., & Bertolasi, V. (2016) · Polyhedron · doi:10.1016/j.poly.2016.04.008 · Cited by 15

Comparing Strong and Weak Halogen Bonding in Solution: 13C NMR, UV/Vis, Crystallographic, and Computational Studies of an Intramolecular Model

Widner, D. L., Robinson, E. R. T., Perez, A. B., Vang, H. G., Thorson, R. A., Driscoll, Z. L., Giebel, S. M., Berndt, C. W., Bosch, E., Speetzen, E. D., et al. (2017) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201700969 · Cited by 15

Tridentate C–I⋯O − –N + halogen bonds

Topić, F., Puttreddy, R., Rautiainen, J. M., Tuononen, H. M., & Rissanen, K. T. (2017) · CrystEngComm · doi:10.1039/c7ce01381g · Cited by 15

Static Modulation Wave of Arrays of Halogen Interactions Transduced to a Hierarchy of Nanoscale Change Stimuli of Crystalline Rotors Dynamics

Simonov, S. V., Zorina, L. V., Wzietek, P., Rodríguez‐Fortea, A., Cañadell, E., Meźière, C., Bastien, G., Lemouchi, C., Garcı́a-Garibay, M. A., & Batail, P. (2018) · Nano Letters · doi:10.1021/acs.nanolett.8b00956 · Cited by 15

The features of iodine loss at high temperatures

Юшина, И. Д., Pikhulya, D. G., & Bartashevich, E. V. (2019) · Journal of Thermal Analysis and Calorimetry · doi:10.1007/s10973-019-08442-y · Cited by 15

Merocyanines in a Halogen-Bonded Network Involving Inorganic Building Blocks

Seiler, V. K., Tumanov, N. A., Robeyns, K., Champagne, B. R., Wouters, J., & Leyssens, T. (2019) · Crystal Growth & Design · doi:10.1021/acs.cgd.9b00903 · Cited by 15

Halogen-bonded cocrystals of donepezil with perfluorinated diiodobenzenes

Nemec, V., Vitasović, T., & Cinčić, D. (2020) · CrystEngComm · doi:10.1039/d0ce01065k · Cited by 15

Probing the halogen bond donation ability of multivalent At-center in AtXn (X = Cl, Br, I; n = 1, 3, 5)⋯H2O/H2S complexes

Yang, Q., Liu, Y., Zhang, Z., Zhou, F., Wang, Z., Zheng, B., & Lu, T. (2020) · Computational and Theoretical Chemistry · doi:10.1016/j.comptc.2020.113090 · Cited by 15

Endocrine-disrupting pollutants properties affecting their bioactivity, remediation, and detection

Dichiarante, V., Cavallo, G., & Metrangolo, P. (2021) · Current Opinion in Green and Sustainable Chemistry · doi:10.1016/j.cogsc.2021.100485 · Cited by 15

Dramatically Enhanced Solubility of Halide‐Containing Organometallic Species in Diiodomethane: The Role of Solvent⋅⋅⋅Complex Halogen Bonding

Kinzhalov, M. A., Kashina, M. V., Mikherdov, A. S., Mozheeva, E. A., Novikov, A. S., Смирнов, С. Н., Ivanov, D. M., Kryukova, M. A., Ivanov, A. Y., Smirnov, S. N., et al. (2018) · Angewandte Chemie · doi:10.1002/ange.201807642 · Cited by 15

On the opposite trends of correlations between interaction energies and electrostatic potentials of chlorinated and methylated amine complexes stabilized by halogen bond

Zierkiewicz, W., & Michalczyk, M. (2017) · Theoretical Chemistry Accounts · doi:10.1007/s00214-017-2145-4 · Cited by 14

Reassessing the Role of σ Holes in Noncovalent Interactions: It is Pauli Repulsion that Counts

Szczęśniak, M. M., & Chałasiński, G. (2022) · Frontiers in Chemistry · doi:10.3389/fchem.2022.858946 · Cited by 14

Unexplored σ-hole and π-hole interactions in (X2CY)2 complexes (X = F, Cl; Y = O, S)

Ibrahim, M. A. A., Saeed, R. R. A., Shehata, M. N. I., Mohamed, E. E. B., Soliman, M. E. S., Al-Fahemi, J. H. A., El-Mageed, H. R. A., Ahmed, M. N., Shawky, A. M., & Moussa, N. A. M. (2022) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2022.133232 · Cited by 14

Investigation of structural, spectral, and electronic properties of complexes resulting from the interaction of acetonitrile and hypohalous acids

Moradkhani, M., Naghipour, A., & Tyula, Y. A. (2023) · Structural Chemistry · doi:10.1007/s11224-023-02243-8 · Cited by 14

Halogen-Bond-Based Organocatalysis Unveiled: Computational Design and Mechanistic Insights

Melnyk, N., Garcia, M. R., & Trujillo, C. (2023) · ACS Catalysis · doi:10.1021/acscatal.3c04035 · Cited by 14

Electrostatic Surface Potentials and Chalcogen‐Bonding Motifs of Substituted 2,1,3‐Benzoselenadiazoles Probed via 77Se Solid‐State NMR Spectroscopy

Georges, T., Ovens, J. S., & Bryce, D. L. (2024) · Chemistry - A European Journal · doi:10.1002/chem.202402254 · Cited by 14

Ortho ‐Carborane‐Derived Halogen Bonding Organocatalysts

Vonnemann, C. J., Engelage, E., Ward, J. S., Rissanen, K. T., Keller, S., & Huber, S. M. (2025) · Angewandte Chemie International Edition · doi:10.1002/anie.202424072 · Cited by 14

Synthesis of tetrahalide dianions directed by crystal engineering

Pan, F., Puttreddy, R., Rissanen, K. T., & Englert, U. (2015) · CrystEngComm · doi:10.1039/c5ce01288k · Cited by 14

Predictive Models for Halogen‐bond Basicity of Binding Sites of Polyfunctional Molecules

Glavatskikh, M., Madzhidov, T., Solov’ev, V. P., Marcou, G., Horvath, D., Graton, J., Questel, J. L., & Varnek, A. A. (2015) · Molecular Informatics · doi:10.1002/minf.201500116 · Cited by 14

A combined experimental and computational study of supramolecular assemblies in two photoluminescent cadmium(II) complexes with halosalicylaldimine Schiff bases

Roy, S., Bauzá, A., Frontera, A., & Chattopadhyay, S. (2016) · Inorganica Chimica Acta · doi:10.1016/j.ica.2016.05.030 · Cited by 14

Development of a pharmacophore for cruzain using oxadiazoles as virtual molecular probes: quantitative structure–activity relationship studies

de Souza, A. S., de Oliveira, M. T., & Andricopulo, A. D. (2017) · Journal of Computer-Aided Molecular Design · doi:10.1007/s10822-017-0039-0 · Cited by 14

A Simple Model for Halogen Bond Interaction Energies

Shaw, R. A., & Hill, J. G. (2019) · Inorganics · doi:10.3390/inorganics7020019 · Cited by 14

Unravelling the Importance of H bonds, σ–hole and π–hole-Directed Intermolecular Interactions in Nature

Pramanik, S., & Chopra, D. (2019) · Journal of the Indian Institute of Science · doi:10.1007/s41745-019-00144-6 · Cited by 14

Virtual Tensile Test for Brittle, Plastic, and Elastic Polymorphs of 4-Bromophenyl 4-Bromobenzoate

Masunov, A. E., Wiratmo, M., Dyakov, A. A., Matveychuk, Y. V., & Bartashevich, E. V. (2020) · Crystal Growth & Design · doi:10.1021/acs.cgd.0c00798 · Cited by 14

Reliable Comparison of Pnicogen, Chalcogen, and Halogen Bonds in Complexes of 6-OXF2-Fulvene (X = As, Sb, Se, Te, Be, I) With Three Electron Donors

Liu, N., Li, Q., & McDowell, S. A. C. (2020) · Frontiers in Chemistry · doi:10.3389/fchem.2020.608486 · Cited by 14

Azo synthesis meets molecular iodine catalysis

Rowshanpour, R., & Dudding, T. C. (2021) · RSC Advances · doi:10.1039/d1ra00369k · Cited by 14

Ligand Steric Hindrances Switch Bridging (μ2-I)···O,O to Two-Center I···O Halogen-Bonding Mode in the Assembly of Diketonate Copper(II) Species

Rozhkov, A. V., Ananyev, I. V., Petrov, A. A., Galmés, B., Frontera, A., Bokach, N. A., & Kukushkin, V. Y. (2021) · Crystal Growth & Design · doi:10.1021/acs.cgd.1c00373 · Cited by 14

Chalcogen Bonding in Co-Crystals: Activation through 1,4-Perfluorophenylene vs. 4,4′-Perfluorobiphenylene Cores

Dhaka, A., Jeannin, O., Aubert, E., Espinosa, E., & Fourmigué, M. (2021) · Molecules · doi:10.3390/molecules26134050 · Cited by 14

Investigation of [CHCl3-CH3OH] complex using matrix-isolation IR spectroscopy and quantum chemical calculation: Evidence of hydrogen- and halogen-bonding interaction

Pal, D., Chakraborty, A., & Chakraborty, S. (2022) · Chemical Physics · doi:10.1016/j.chemphys.2022.111451 · Cited by 14

Guest‐Induced Structural Transformations in a Porous Halogen‐Bonded Framework

Nikolayenko, V. I., Castell, D. C., van Heerden, D. P., & Barbour, L. J. (2018) · Angewandte Chemie · doi:10.1002/ange.201806399 · Cited by 14

A Crystallographic Charge Density Study of the Partial Covalent Nature of Strong N⋅⋅⋅Br Halogen Bonds

Eraković, M., Cinčić, D., Molčanov, K., & Stilinović, V. (2019) · Angewandte Chemie · doi:10.1002/ange.201908875 · Cited by 14

DFT potentials from a chemical perspective: Anatomy of electron (de)localization in molecules and crystals

Levina, E. O., & Григорьевич, Ц. В. (2023) · Journal of Computational Chemistry · doi:10.1002/jcc.27131 · Cited by 14

Comparison of halogen bonds in M−X⋯N contacts (M=C, Si, Ge and X=Cl, Br)

Jahromi, H. J., Eskandari, K., & Alizadeh, A. (2015) · Journal of Molecular Modeling · doi:10.1007/s00894-015-2660-y · Cited by 14

Halogen effects on the solid-state packing of phenylalanine derivatives and the resultant gelation properties

Ramalhete, S. M., Foster, J. S., Green, H. R., Nartowski, K. P., Heinrich, M., Martin, P. C., Khimyak, Y. Z., & Lloyd, G. O. (2017) · Faraday Discussions · doi:10.1039/c7fd00108h · Cited by 14

Structural Diversity in a New Series of Halogenated Quinolyl Salicylaldimides-Based FeIII Complexes Showing Solid-State Halogen-Bonding/Halogen···Halogen Interactions

Sahadevan, S. A., Cadoni, E., Monni, N., de Pipaón, C. S., Galán‐Mascarós, J. R., Abhervé, A., Avarvari, N., Marchiò, L., Arca, M., & Mercuri, M. L. (2018) · Crystal Growth & Design · doi:10.1021/acs.cgd.8b00753 · Cited by 14

Organic molecular tessellations and intertwined double helices assembled by halogen bonding

Ng, C., Chow, H., & Mak, T. C. W. (2019) · CrystEngComm · doi:10.1039/c8ce02133c · Cited by 14

Hydrogen Bond versus Halogen Bond in HXOn (X = F, Cl, Br, and I) Complexes with Lewis Bases

Quiñonero, D., & Frontera, A. (2019) · Inorganics · doi:10.3390/inorganics7010009 · Cited by 14

Identification of an Overlooked Halogen‐Bond Synthon and Its Application in Designing Fluorescent Materials

Lu, C., Zhu, B., Ma, X., Zhang, Z., Wang, J., Zhang, Q., & Mei, X. (2019) · Chemistry - A European Journal · doi:10.1002/chem.201900371 · Cited by 14

Highly functionalised (γ-azido/γ-fluoro-β-iodo/)vinyl derivatives from phosphorus based allenes or allenoates: I⋯O halogen bonding interactions

Anitha, M., & Swamy, K. C. K. (2019) · Organic & Biomolecular Chemistry · doi:10.1039/c9ob00715f · Cited by 14

Correlation of the partial charge-transfer and covalent nature of halogen bonding with the THz and IR spectral changes

Torii, H. (2019) · Physical Chemistry Chemical Physics · doi:10.1039/c9cp02747e · Cited by 14

Structures and Chemical Bonding in Antimony(III) Bromide Complexes with Pyridine

Prokudina, Y. V., Davydova, E. I., Virovets, A. V., Stöger, B., Peresypkina, E. V., Pomogaeva, A. V., & Timoshkin, A. Y. (2020) · Chemistry - A European Journal · doi:10.1002/chem.202002261 · Cited by 14

Pentavalent P…π phosphorus bonding with associated Cl…π halogen bonding in influencing the geometry of POCl3-Phenylacetylene heterodimers: Evidence from matrix isolation infrared spectroscopy and ab initio computations

Suryaprasad, B., Chandra, S., Ramanathan, N., & Sundararajan, K. (2020) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2020.129288 · Cited by 14

DFT and IsoStar Analyses to Assess the Utility of σ‐ and π‐Hole Interactions for Crystal Engineering

Mooibroek, T. J. (2020) · ChemPhysChem · doi:10.1002/cphc.202000927 · Cited by 14

Heteroleptic Cu(I) halide complexes with perchlorinated 1,10-phenanthroline

Bondarenko, M. A., Novikov, A. S., Sakhapov, I. F., Sokolov⧫, M. N., & Adonin, S. A. (2021) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2021.130199 · Cited by 14

Halogen bond interaction: Role of hybridization and induction

Nunzi, F., Cesario, D., Tarantelli, F., & Belpassi, L. (2021) · Chemical Physics Letters · doi:10.1016/j.cplett.2021.138522 · Cited by 14

Halogen Bonding in the Design of Organic Phosphors

Pang, X., & Jin, W. J. (2014) · Topics in current chemistry · doi:10.1007/128_2014_614 · Cited by 14

Concerted Halogen Bonding and Orthogonal Metal-Halogen Interactions in Dimers of Lithium Formamidinate and Halogenated Formamidines: An ab Initio Study

Parra, R. D. (2014) · Molecules · doi:10.3390/molecules19011069 · Cited by 14

A Raman Spectroscopic and Computational Study of New Aromatic Pyrimidine-Based Halogen Bond Acceptors

Hardin, A. E., Ellington, T. L., Nguyen, S. T., Rheingold, A. L., Tschumper, G. S., Watkins, D. L., & Hammer, N. I. (2019) · Inorganics · doi:10.3390/inorganics7100119 · Cited by 13

Theoretical rationale for the role of the strong halogen bond in the design and synthesis of organic semiconductor materials

Zhang, Y., & Wang, W. (2020) · Computational and Theoretical Chemistry · doi:10.1016/j.comptc.2020.113074 · Cited by 13

The Electrophilicities of XCF 3 and XCl (X=H, Cl, Br, I) and the Propensity of These Molecules To Form Hydrogen and Halogen Bonds with Lewis Bases: An Ab Initio Study

Alkorta, I., & Legon, A. C. (2021) · ChemPlusChem · doi:10.1002/cplu.202100088 · Cited by 13

Composite of methyl polysiloxane and avocado biochar as adsorbent for removal of ciprofloxacin from waters

Teixeira, R. A., Lima, E. C., Benetti, A. D., Thue, P. S., Lima, D. R., Sher, F., dos Reis, G. S., Rabiee, N., Seliem, M. K., & Abatal, M. (2022) · Environmental Science and Pollution Research · doi:10.1007/s11356-022-21176-z · Cited by 13

I⋯N halogen bonding in 1 : 1 co-crystals formed between 1,4-diiodotetrafluorobenzene and the isomeric n -pyridinealdazines ( n = 2, 3 and 4): assessment of supramolecular association and influence upon solid-state photoluminescence properties

Yeo, C. I., Tan, Y. S., Kwong, H. C., Lee, V. S., & Tiekink, E. R. T. (2022) · CrystEngComm · doi:10.1039/d2ce01165d · Cited by 13

The role of halogen bonding in the interaction landscape directing the crystal packing in a homologous series of halogenated coumarin derivatives

Popa, M. M., Dumitrescu, D. G., Shova, S. G., Man, I. C., van der Lee, A., & Dumitraşcu, F. (2023) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2023.136112 · Cited by 13

Solution Studies of a Water-Stable, Trivalent Antimony Pnictogen Bonding Anion Receptor with High Binding Affinities for CN – , OCN – , and OAc –

Qiu, J., Bateman, C. N., Lü, S., George, G. C., Li, X., Gorden, J. D., Vasylevskyi, S., & Cozzolino, A. F. (2023) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.3c01887 · Cited by 13

Hydrogen vs Halogen-Bonded R22(8) Rings in Organic Crystal Structures

Esterhuysen, C. (2023) · Crystal Growth & Design · doi:10.1021/acs.cgd.3c01343 · Cited by 13

Elucidating the Role of Electron-Donating Groups in Halogen Bonding

Devore, D. P., Ellington, T. L., & Shuford, K. L. (2024) · The Journal of Physical Chemistry A · doi:10.1021/acs.jpca.3c06894 · Cited by 13

Fabrication strategies for chiral self-assembly surface

Niu, X., Yuan, M., Zhao, R., Wang, L., Liu, Y., Zhao, H., Li, H., Yang, X., & Wang, K. (2024) · Microchimica Acta · doi:10.1007/s00604-024-06278-4 · Cited by 13

Halogen Bond via an Electrophilic π-Hole on Halogen in Molecules: Does It Exist?

Varadwaj, P. R. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094587 · Cited by 13

Interplay of a nitro group and metal ions: from coordinative binding to noncovalent semicoordination

Suslonov, V. V., Soldatova, N. S., Ivanov, D. M., Постников, П. С., Gomila, R. M., Frontera, A., Semenov, A. V., Kukushkin, V. Y., & Bokach, N. A. (2024) · Inorganic Chemistry Frontiers · doi:10.1039/d4qi00351a · Cited by 13

Halogen Bonding in Perfluoroalkyl Adsorption

Lü, L., & Na, C. (2024) · ACS Omega · doi:10.1021/acsomega.4c01367 · Cited by 14

halogen bond

(2024) · International Union of Pure and Applied Chemistry (IUPAC) eBooks · doi:10.1351/goldbook.08173

IUPAC definition of the halogen bond

Metrangolo, P. (2017) · Acta Crystallographica Section A Foundations and Advances · doi:10.1107/s2053273317092646 · Cited by 2

Definition der Halogenbrücke (IUPAC‐Empfehlungen 2013)

Schmuck, C., & Weber, E. (2014) · Angewandte Chemie · doi:10.1002/ange.201309626 · Cited by 3

Halogen bonding and other noncovalent interactions involving halogens: a terminology issue

Metrangolo, P., Pilati, T., & Resnati, G. (2006) · CrystEngComm · doi:10.1039/b610454a · Cited by 162

Ionic, hydrogen or halogen bonds? Relevance for predicting crystal structures

Price, S. L. (2011) · Acta Crystallographica Section A Foundations of Crystallography · doi:10.1107/s0108767311096668