The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Definition of the halogen bond (IUPAC Recommendations 2013).
Open accessAbstract
This recommendation proposes a definition for the term “halogen bond”, which designates a specific subset of the inter- and intramolecular interactions involving a halogen atom in a molecular entity.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Many studies have highlighted the influence of halogen bonds (X-bonds) on enhancing binding affinity against several targets and the computational methods developed so far (Desiraju et al., 2013; Ford and Ho, 2016).”
From Empirical scoring functions for structure-based virtual screening: applications, critical aspects, and challenges (2018) · cites this paper as Desiraju et al., 2013
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
Cited by
Sorted by citations
Items 701–800 of 1,000
Short X···N Halogen Bonds With Hexamethylenetetraamine as the Acceptor
Anyfanti, G., Bauzá, A., Gentiluomo, L., Rodrigues, J., Portalone, G., Frontera, A., Rissanen, K. T., & Puttreddy, R. (2021) · Frontiers in Chemistry · doi:10.3389/fchem.2021.623595 · Cited by 23
Self-citationDang, Q. M., Simpson, J. H., Parish, C. A., & Leopold, M. C. (2021) · The Journal of Physical Chemistry A · doi:10.1021/acs.jpca.1c07554 · Cited by 23
NMR Response of the Tetrel Bond Donor
Southern, S. A., Nag, T., Kumar, V., Triglav, M., Levin, K., & Bryce, D. L. (2021) · The Journal of Physical Chemistry C · doi:10.1021/acs.jpcc.1c10121 · Cited by 23
[N⋅⋅⋅I+⋅⋅⋅N] Halogen‐Bonded Dimeric Capsules from Tetrakis(3‐pyridyl)ethylene Cavitands
Turunen, L., Warzok, U., Puttreddy, R., Beyeh, N. K., Schalley, C. A., & Rissanen, K. T. (2016) · Angewandte Chemie · doi:10.1002/ange.201607789 · Cited by 23
Self-citationAn Adaptable and Dynamically Porous Organic Salt Traps Unique Tetrahalide Dianions
Martí‐Rujas, J., Meazza, L., Lim, G. K., Terraneo, G., Pilati, T., Harris, K. D. M., Metrangolo, P., & Resnati, G. (2013) · Angewandte Chemie · doi:10.1002/ange.201307552 · Cited by 23
Self-citationPeriodate anions as a halogen bond donor: formation of anion⋯anion dimers and other adducts
Calabrese, M., Pizzi, A., Daolio, A., Frontera, A., & Resnati, G. (2022) · Chemical Communications · doi:10.1039/d2cc03191d · Cited by 23
Self-citationA Quantum‐chemical Analysis on the Lewis Acidity of Diarylhalonium Ions
Robidas, R., Reinhard, D. L., Huber, S. M., & Legault, C. Y. (2022) · ChemPhysChem · doi:10.1002/cphc.202200634 · Cited by 23
Matere Bonds vs. Multivalent Halogen and Chalcogen Bonds: Three Case Studies
Gomila, R. M., & Frontera, A. (2022) · Molecules · doi:10.3390/molecules27196597 · Cited by 23
Dutta, B., Ahmed, F., & Mir, M. H. (2022) · Crystal Growth & Design · doi:10.1021/acs.cgd.2c00908 · Cited by 23
Halogen‐Bonded Liquid Crystals
Präsang, C., & Bruce, D. W. (2023) · Helvetica Chimica Acta · doi:10.1002/hlca.202300008 · Cited by 23
Halogen and Hydrogen Bonded Complexes of 5-Iodouracil
Valkonen, A., Chukhlieb, M., Moilanen, J. O., Tuononen, H. M., & Rissanen, K. T. (2013) · Crystal Growth & Design · doi:10.1021/cg400924n · Cited by 23
Self-citationFormation of Self-Complementary Halogen-Bonded Dimers
Oburn, S. M., Bowling, N. P., & Bosch, E. (2015) · Crystal Growth & Design · doi:10.1021/cg501406w · Cited by 23
Quantifying the Effects of Halogen Bonding by Haloaromatic Donors on the Acceptor Pyrimidine
Ellington, T. L., Reves, P. L., Simms, B. L., Wilson, J. L., Watkins, D. L., Tschumper, G. S., & Hammer, N. I. (2017) · ChemPhysChem · doi:10.1002/cphc.201700114 · Cited by 23
Mosquera, M. E. G., Egido, I., Hortelano, C., López-López, M., & Gómez‐Sal, P. (2017) · Faraday Discussions · doi:10.1039/c7fd00079k · Cited by 23
Supramolecular control of liquid crystals by doping with halogen-bonding dyes
Vapaavuori, J., Siiskonen, A., Dichiarante, V., Forni, A., Saccone, M., Pilati, T., Pellerin, C., Shishido, A., Metrangolo, P., & Priimägi, A. (2017) · RSC Advances · doi:10.1039/c7ra06397k · Cited by 23
Self-citationRestricted Speciation and Supramolecular Assembly in the 5f Block
Carter, K. P., Surbella, R. G., Kalaj, M., & Cahill, C. L. (2018) · Chemistry - A European Journal · doi:10.1002/chem.201801044 · Cited by 23
Kukkonen, E., Malinen, H., Haukka, M., & Konu, J. (2019) · Crystal Growth & Design · doi:10.1021/acs.cgd.9b00119 · Cited by 23
Khavasi, H. R., & Rahimi, N. (2016) · Crystal Growth & Design · doi:10.1021/acs.cgd.6b01673 · Cited by 22
Ibrahim, M. A., El‐Alfy, A. T., Ezel, K., Radwan, M. O., Shilabin, A. G., Kochanowska-Karamyan, A. J., Abd-Alla, H. I., Otsuka, M., & Hamann, M. T. (2017) · Marine Drugs · doi:10.3390/md15080248 · Cited by 23
Molecular iodine as a mild catalyst for cross-coupling of alkenes and alcohols
Čebular, K., & Stavber, S. (2018) · Pure and Applied Chemistry · doi:10.1515/pac-2017-0414 · Cited by 22
Bauzá, A., Quiñonero, D., & Frontera, A. (2017) · Molecules · doi:10.3390/molecules23010018 · Cited by 22
Halogen bonded metal bis(dithiolene) 2D frameworks
Hachem, H., Jeannin, O., Fourmigué, M., Barrière, F., & Lorcy, D. (2020) · CrystEngComm · doi:10.1039/d0ce00512f · Cited by 22
Alkorta, I., Silva, A. F., & Popelier, P. L. A. (2020) · Molecules · doi:10.3390/molecules25112674 · Cited by 22
Iodine(I) and Silver(I) Complexes of Benzoimidazole and Pyridylcarbazole Derivatives
Taipale, E., Siepmann, M., Truong, K., & Rissanen, K. T. (2021) · Chemistry - A European Journal · doi:10.1002/chem.202103152 · Cited by 22
Self-citationIshigaki, Y., Shimomura, K., Asai, K., Shimajiri, T., Akutagawa, T., Fukushima, T., & Suzuki, T. (2022) · Bulletin of the Chemical Society of Japan · doi:10.1246/bcsj.20220008 · Cited by 22
Supramolecular networks by imine halogen bonding
Nieland, E., Komisarek, D., Hohloch, S., Wurst, K., Vasylyeva, V., Weingart, O., & Schmidt, B. M. (2022) · Chemical Communications · doi:10.1039/d2cc00799a · Cited by 22
Halogen‐Bond‐Assisted Guest Inclusion in a Synthetic Cavity
Takezawa, H., Murase, T., Resnati, G., Metrangolo, P., & Fujita, M. (2015) · Angewandte Chemie · doi:10.1002/ange.201500994 · Cited by 22
Self-citationMontgomery, C. A., & Murphy, G. K. (2023) · Beilstein Journal of Organic Chemistry · doi:10.3762/bjoc.19.86 · Cited by 22
Radzhabov, A. D., Ledneva, A. Y., Soldatova, N. S., Fedorova, I. I., Ivanov, D. M., Ivanov, A. A., Yusubov, M. S., Kukushkin, V. Y., & Постников, П. С. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914642 · Cited by 22
Cheranyova, A. M., Zelenkov, L. E., Baykov, S. V., Izotova, Y. A., Ivanov, D. M., Bokach, N. A., & Kukushkin, V. Y. (2024) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.4c01570 · Cited by 23
Isostructural Co-crystals Derived from Molecules with Different Supramolecular Topologies
Pfrunder, M. C., Micallef, A. S., Rintoul, L., Arnold, D. P., Davy, K. J. P., & McMurtrie, J. C. (2014) · Crystal Growth & Design · doi:10.1021/cg501210t · Cited by 22
Electrochemical controlling and monitoring of halogen bond formation in solution
Groni, S., Maby-Raud, T., Fave, C., Branca, M., & Schöllhorn, B. (2014) · Chemical Communications · doi:10.1039/c4cc04134h · Cited by 22
Halogen Bonds in Square Planar 2,5‐Dihalopyridine–Copper(II) Bromide Complexes
Puttreddy, R., von Eßen, C., & Rissanen, K. T. (2018) · European Journal of Inorganic Chemistry · doi:10.1002/ejic.201800144 · Cited by 22
Self-citationDu, M., Li, L., Zhang, J., Li, K., Cao, M., Mo, L., Hu, G., Chen, Y., Yu, H., & Yang, H. (2018) · Liquid Crystals · doi:10.1080/02678292.2018.1468040 · Cited by 22
Halogen bonding driven crystal engineering of iodophthalonitrile derivatives
Ateş, Ö. D., Zorlu, Y., Kanmazalp, S. D., Chumakov, Y. M., Gürek, A. G., & Ayhan, M. M. (2018) · CrystEngComm · doi:10.1039/c8ce00594j · Cited by 22
Zhang, Y. L., Wang, W., & Wang, Y. (2018) · Computational and Theoretical Chemistry · doi:10.1016/j.comptc.2018.11.011 · Cited by 22
Chalcogen Bonds in Crystals of Bis(o-anilinium)diselenide Salts
Scilabra, P., Murray, J. S., Terraneo, G., & Resnati, G. (2018) · Crystal Growth & Design · doi:10.1021/acs.cgd.8b01634 · Cited by 24
Self-citationModulating the intrinsic reactivity of molecules through non-covalent interactions
Montero‐Campillo, M. M., Brea, O., Mó, O., Alkorta, I., Elguero, J., & Yáñez, M. (2019) · Physical Chemistry Chemical Physics · doi:10.1039/c8cp06908e · Cited by 22
Ghosh, T. K., Mondal, S., Bej, S., Nandi, M., & Ghosh, P. (2019) · Dalton Transactions · doi:10.1039/c8dt05066j · Cited by 22
Recent Advances in Halogen Bond-assisted Organic Synthesis
Yamada, S., & Konno, T. (2019) · Current Organic Chemistry · doi:10.2174/1385272823666191209112543 · Cited by 22
Frontera, A. (2020) · Crystals · doi:10.3390/cryst10090721 · Cited by 22
Quentin, J., & MacGillivray, L. R. (2020) · Crystal Growth & Design · doi:10.1021/acs.cgd.0c01143 · Cited by 22
The Supramolecular Structural Chemistry of Pentafluorosulfanyl and Tetrafluorosulfanylene Compounds
Liebing, P., Pitts, C. R., Reimann, M., Trapp, N., Rombach, D., Bornemann, D., Kaupp, M., & Togni, A. (2021) · Chemistry - A European Journal · doi:10.1002/chem.202100163 · Cited by 22
The Influence of Secondary Interactions on the [N−I−N]+ Halogen Bond
Lindblad, S., Németh, F. B., Földes, T., von der Heiden, D., Vang, H. G., Driscoll, Z. L., Gonnering, E. R., Pápai, I., Bowling, N. P., & Erdélyi, M. (2021) · Chemistry - A European Journal · doi:10.1002/chem.202102575 · Cited by 22
Flexible Alkali–Halogen Bonding in Two Dimensional Alkali-Metal Organic Frameworks
Shan, H., Zhou, L., Ji, W., & Zhao, A. (2021) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.1c03069 · Cited by 22
Halogen bonding in functional chiral systems
An, S., & Xing, P. (2026) · Chemical Society Reviews · doi:10.1039/d5cs00938c · Cited by 23
Halogen Bonds in Clathrate Cages: A Real Space Perspective
Guevara‐Vela, J. M., Ochoa‐Resendiz, D., Costales, A., Hernández‐Lamoneda, R., & Pendás, Á. M. (2018) · ChemPhysChem · doi:10.1002/cphc.201800474 · Cited by 21
Synthesis of Chiral Triazole-Based Halogen Bond Donors
Kaasik, M., Kaabel, S., Kriis, K., Järving, I., & Kanger, T. (2019) · Synthesis · doi:10.1055/s-0037-1610864 · Cited by 21
Varadwaj, A., Marques, H. M., & Varadwaj, P. R. (2019) · Journal of Computational Chemistry · doi:10.1002/jcc.25836 · Cited by 21
Gatti, C., Dessì, A., Dallocchio, R. N., Mamane, V., Cossu, S., Weiss, R., Pale, P., Aubert, E., & Peluso, P. (2020) · Molecules · doi:10.3390/molecules25194409 · Cited by 21
Katkova, S. A., Mikherdov, A. S., Sokolova, E. V., Novikov, A. S., Старова, Г. Л., & Kinzhalov, M. A. (2021) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2021.132230 · Cited by 21
Aliyarova, I. S., Tupikina, E. Y., Ivanov, D. M., & Kukushkin, V. Y. (2022) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.1c03482 · Cited by 21
Halogen Bonding Helicates Encompassing Iodonium Cations
Vanderkooy, A., Gupta, A. K., Földes, T., Lindblad, S., Orthaber, A., Pápai, I., & Erdélyi, M. (2019) · Angewandte Chemie · doi:10.1002/ange.201904817 · Cited by 21
Chakalov, E. R., Tupikina, E. Y., Ivanov, D. M., Bartashevich, E. V., & Tolstoy, P. M. (2022) · Molecules · doi:10.3390/molecules27154848 · Cited by 21
Tetrel Bonding in Anion Recognition: A First Principles Investigation
Varadwaj, P. R. (2022) · Molecules · doi:10.3390/molecules27238449 · Cited by 21
Cunha, A. V., Havenith, R. W. A., van Gog, J., Vleeschouwer, F. D., Proft, F. D., & Herrebout, W. (2023) · Molecules · doi:10.3390/molecules28020772 · Cited by 21
Halogen-Bonded [N–I–N]− Complexes with Symmetric or Asymmetric Three-Center–Four-Electron Bonds
Yu, S., Truong, K., Siepmann, M., Siiri, A., Schumacher, C., Ward, J. S., & Rissanen, K. T. (2023) · Crystal Growth & Design · doi:10.1021/acs.cgd.2c01162 · Cited by 21
Self-citationSun, D., Zhi-min, W., Zhang, X., Yang, J., Zhao, Y., Nam, W., & Wang, Y. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.2c12307 · Cited by 21
Gulyaev, R., Semyonov, O., Mamontov, G. V., Ivanov, A. A., Ivanov, D. M., Kim, M., Švorčı́k, V., Resnati, G., Liao, T., Sun, Z., et al. (2023) · ACS Materials Letters · doi:10.1021/acsmaterialslett.2c01169 · Cited by 21
Self-citationN−X⋅⋅⋅O−N Halogen Bonds in Complexes of N‐Haloimides and Pyridine‐N‐oxides: A Large Data Set Study
Puttreddy, R., Rautiainen, J. M., Yu, S., & Rissanen, K. T. (2023) · Angewandte Chemie International Edition · doi:10.1002/anie.202307372 · Cited by 21
Self-citationThe halogen bond in thiirane⋯ClF: an example of a Mulliken inner complex
Hill, J. G. (2014) · Physical Chemistry Chemical Physics · doi:10.1039/c4cp03412k · Cited by 21
125 Te NMR provides evidence of autoassociation of organo-ditellurides in solution
Elder, P. J. W., & Vargas‐Baca, I. (2016) · Physical Chemistry Chemical Physics · doi:10.1039/c6cp05892b · Cited by 21
Synthesis and Characterization of Nonclassical Interhalides Based on Bromine Monochloride
Schmidt, B. W., Sonnenberg, K., Beckers, H., Steinhauer, S., & Riedel, S. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201803705 · Cited by 21
Superfluorinated Ionic Liquid Crystals Based on Supramolecular, Halogen‐Bonded Anions
Cavallo, G., Terraneo, G., Monfredini, A., Saccone, M., Priimägi, A., Pilati, T., Resnati, G., Metrangolo, P., & Bruce, D. W. (2016) · Angewandte Chemie · doi:10.1002/ange.201601278 · Cited by 21
Self-citationFrom Polyhalides to Polypseudohalides: Chemistry Based on Cyanogen Bromide
Schmidt, B. W., Schröder, B., Sonnenberg, K., Steinhauer, S., & Riedel, S. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201903539 · Cited by 20
O–I–O halogen bond of halonium ions
Lindblad, S., Németh, F. B., Földes, T., Vanderkooy, A., Pápai, I., & Erdélyi, M. (2020) · Chemical Communications · doi:10.1039/d0cc03513k · Cited by 20
Frontera, A., & Bauzá, A. (2021) · Organic & Biomolecular Chemistry · doi:10.1039/d1ob01212f · Cited by 20
Kinzhalov, M. A., Ivanov, D. M., Melekhova, A. A., Bokach, N. A., Gomila, R. M., Frontera, A., & Kukushkin, V. Y. (2022) · Inorganic Chemistry Frontiers · doi:10.1039/d2qi00034b · Cited by 20
Crystal Structure and Noncovalent Interactions of Heterocyclic Energetic Molecules
Liu, Y., Fan, J., Xue, Z., Lu, Y., Zhao, J., & Hui, W. (2022) · Molecules · doi:10.3390/molecules27154969 · Cited by 20
Sutradhar, D., Chandra, A. K., & Zeegers‐Huyskens, T. (2016) · International Journal of Quantum Chemistry · doi:10.1002/qua.25083 · Cited by 20
Wang, L., Gao, J., Bi, F., Song, B., & Liu, C. (2014) · The Journal of Physical Chemistry A · doi:10.1021/jp502739c · Cited by 20
Intramolecular halogen bonding: an interacting quantum atoms study
Yahia-Ouahmed, M., Tognetti, V., & Joubert, L. (2016) · Theoretical Chemistry Accounts · doi:10.1007/s00214-015-1796-2 · Cited by 20
Nicolas, I., Jeannin, O., Pichon, D., & Fourmigué, M. (2016) · CrystEngComm · doi:10.1039/c6ce02175a · Cited by 20
Self‐Assembly of Iodine in Superfluid Helium Droplets: Halogen Bonds and Nanocrystals
He, Y., Zhang, J., Lei, L., & Kong, W. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201611922 · Cited by 20
The role of halogen bonding in improving OFET performance of a naphthalenediimide derivative
Li, J., Hu, Y.-H., Ge, C., Gong, H., & Gao, X. (2017) · Chinese Chemical Letters · doi:10.1016/j.cclet.2017.06.008 · Cited by 20
Balmohammadi, Y., Khavasi, H. R., & Naghavi, S. S. (2020) · CrystEngComm · doi:10.1039/c9ce01885a · Cited by 20
Halogen-Bonded Bithiophene-Based Nanofibers for Luminescent Sensing
Ghosh, T. K., Mitra, S., Maity, S. K., & Maiti, D. K. (2020) · ACS Applied Nano Materials · doi:10.1021/acsanm.0c00886 · Cited by 20
Halogen Bond‐Catalyzed Friedel−Crafts Reactions of Furans Using a 2,2’‐Bipyridine‐Based Catalyst
Zhang, H., & Toy, P. H. (2020) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.202001019 · Cited by 20
Ciancaleoni, G., & Rocchigiani, L. (2021) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.0c03650 · Cited by 20
Recent advances in NMR crystallography and polymorphism
Southern, S. A., & Bryce, D. L. (2021) · Annual reports on NMR spectroscopy · doi:10.1016/bs.arnmr.2020.10.001 · Cited by 20
Structure of the Holliday junction: applications beyond recombination
Ho, P. S. (2017) · Biochemical Society Transactions · doi:10.1042/bst20170048 · Cited by 20
Self-citationCharacterization of Halogen Bonded Adducts in Solution by Advanced NMR Techniques
Ciancaleoni, G. (2017) · Magnetochemistry · doi:10.3390/magnetochemistry3040030 · Cited by 19
Joy, J., Akhil, E., & Jemmis, E. D. (2018) · Physical Chemistry Chemical Physics · doi:10.1039/c8cp05125a · Cited by 20
Kazmi, M., Ibrar, A., Ali, H. S., Ghufran, M., Wadood, A., Flörke, Ü., Simpson, J., Saeed, A., Frontera, A., & Khan, I. A. (2019) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2019.07.077 · Cited by 20
Martín−Fernández, C., Montero‐Campillo, M. M., & Alkorta, I. (2024) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.4c00779 · Cited by 20
Oliveira, R. S., Groni, S., Vacher, A., Barrière, F., Lorcy, D., Fourmigué, M., Maisonhaute, E., Schöllhorn, B., & Fave, C. (2018) · ChemistrySelect · doi:10.1002/slct.201801957 · Cited by 19
Sutar, R. L., Engelage, E., Stoll, R., & Huber, S. M. (2020) · Angewandte Chemie · doi:10.1002/ange.201915931 · Cited by 19
Kikkawa, S., Okayasu, M., Hikawa, H., & Azumaya, I. (2020) · Crystal Growth & Design · doi:10.1021/acs.cgd.0c01469 · Cited by 19
Chalcogen bonding mediates the formation of supramolecular helices of azapeptides in crystals
Shi, D., Cao, J., Weng, P., Yan, X., Li, Z., & Jiang, Y. (2021) · Organic & Biomolecular Chemistry · doi:10.1039/d1ob01053k · Cited by 19
Alfuth, J., Zadykowicz, B., Wicher, B., Kazimierczuk, K., Połoński, T., & Olszewska, T. (2022) · Crystal Growth & Design · doi:10.1021/acs.cgd.1c01266 · Cited by 19
Promoting halogen-bonding catalyzed living radical polymerization through ion-pair strain
Huang, S., Su, X., Wu, Y., Xiong, X., & Liu, Y. (2022) · Chemical Science · doi:10.1039/d2sc04196k · Cited by 19
Spodium bonding to anticrown-Hg 3 boosts phosphorescence of cyclometalated-Pt II complexes
Rozhkov, A. V., Katlenok, E. A., Zhmykhova, M. V., Kuznetsov, M. L., Khrustalev, V. N., Tugashov, K. I., Bokach, N. A., & Kukushkin, V. Y. (2022) · Inorganic Chemistry Frontiers · doi:10.1039/d2qi02047e · Cited by 19
Soldatova, N. S., Suslonov, V. V., Ivanov, D. M., Yusubov, M. S., Resnati, G., Постников, П. С., & Kukushkin, V. Y. (2022) · Crystal Growth & Design · doi:10.1021/acs.cgd.2c01090 · Cited by 19
Self-citationπ-Hole Halogen Bonds Are Sister Interactions to σ-Hole Halogen Bonds
Varadwaj, P. R., Marques, H. M., Varadwaj, A., & Yamashita, K. (2024) · Crystal Growth & Design · doi:10.1021/acs.cgd.4c00448 · Cited by 19
A Unified Perspective on the Nature of Bonding in Pairwise Interatomic Interactions
Lucchese, R. R., Rosales, C. K., Rivera−Rivera, L. A., McElmurry, B. A., Bevan, J. W., & Walton, J. R. (2014) · The Journal of Physical Chemistry A · doi:10.1021/jp505985x · Cited by 19
Sedlák, R., Deepa, P., & Hobza, P. (2014) · The Journal of Physical Chemistry A · doi:10.1021/jp502648e · Cited by 19
Mole, T. K., Arter, W. E., Marques, I., Félix, V. M. S., & Beer, P. D. (2015) · Journal of Organometallic Chemistry · doi:10.1016/j.jorganchem.2015.04.039 · Cited by 19
The Role of the Hydroxyl Group in Propofol–Protein Target Recognition: Insights from ONIOM Studies
Qiu, L., Lin, J., Liu, Q., Wang, S., Lv, G., Li, K., Shi, H., Huang, Z., & Bertaccini, E. J. (2017) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.7b02079 · Cited by 19
Bauzá, A., & Frontera, A. (2017) · Crystals · doi:10.3390/cryst7070191 · Cited by 19
Bol’shakov, O., Юшина, И. Д., Bartashevich, E. V., Nelyubina, Y. V., Aysin, R. R., & Rakitin, O. A. (2017) · Structural Chemistry · doi:10.1007/s11224-017-0987-y · Cited by 19
Metadata
- Authors
- Desiraju, G. R., Ho, P. S., Kloo, L., Legon, A. C., Marquardt, R., Metrangolo, P., Politzer, P., Resnati, G., & Rissanen, K.
- Affiliations
- Indian Institute of Science Bangalore (IN)
- Colorado State University (US)
- KTH Royal Institute of Technology (SE)
- University of Bristol (GB)
- Institut de Chimie de Strasbourg (FR)
- Politecnico di Milano (IT)
- CleveTheoComp, 1951 W. 26th Street, Suite 409, Cleveland, OH 44113, USA
- University of Jyväskylä (FI)
- ORCID
- Venue
- Pure and Applied Chemistry
- Publisher
- Walter de Gruyter GmbH
- Published
- 2013-07-10
- Volume
- 85
- Issue
- 8
- Pages
- 1711-1713
- ISSN
- 0033-4545 (ISSN-L)
- 1365-3075
- OpenAlex
- W2094742663
- Cited by
- 1,957
- References
- 2
- Citations by year
- 2026: 103 · 2025: 149 · 2024: 175 · 2023: 155 · 2022: 162 · 2021: 203 · 2020: 187 · 2019: 173 · 2018: 155 · 2017: 144 · 2016: 134 · 2015: 111 · 2014: 87 · 2013: 19
- FWCI
- 73.81
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Pure and Applied Chemistry (publishedVersion)
- NOT FOUND REPOSITORY (Indian Institute of Science Bangalore) (acceptedVersion)
- Virtual Community of Pathological Anatomy (University of Castilla La Mancha) (submittedVersion)
- Topics
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Crystallography and molecular interactions
- Physical Sciences › Chemistry › Spectroscopy › Molecular Spectroscopy and Structure
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Surface Chemistry and Catalysis
- Keywords
- halogen bonding, intermolecular interactions, intramolecular interactions, chemical terminology, IUPAC recommendations
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review