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Extremely short halogen bond: the nature and energy of iodine–oxygen interactions in crystalline iodic acid

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Nelyubina Y. V., Antipin M. Y., Lyssenko K. A. Extremely short halogen bond: the nature and energy of iodine–oxygen interactions in crystalline iodic acid // Mendeleev Communications. 2011. Vol. 21. No. 5. pp. 250-252.
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Nelyubina Y. V., Antipin M. Y., Lyssenko K. A. Extremely short halogen bond: the nature and energy of iodine–oxygen interactions in crystalline iodic acid // Mendeleev Communications. 2011. Vol. 21. No. 5. pp. 250-252.
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TY - JOUR
DO - 10.1016/j.mencom.2011.09.006
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.09.006
TI - Extremely short halogen bond: the nature and energy of iodine–oxygen interactions in crystalline iodic acid
T2 - Mendeleev Communications
AU - Nelyubina, Yulia Vladimirovna
AU - Antipin, Mikhail Yuvenal'evich
AU - Lyssenko, Konstantin Alexandrovich
PY - 2011
DA - 2011/09/14
PB - Mendeleev Communications
SP - 250-252
IS - 5
VL - 21
ER -
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@article{2011_Nelyubina,
author = {Yulia Vladimirovna Nelyubina and Mikhail Yuvenal'evich Antipin and Konstantin Alexandrovich Lyssenko},
title = {Extremely short halogen bond: the nature and energy of iodine–oxygen interactions in crystalline iodic acid},
journal = {Mendeleev Communications},
year = {2011},
volume = {21},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.09.006},
number = {5},
pages = {250--252},
doi = {10.1016/j.mencom.2011.09.006}
}
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Nelyubina, Yulia Vladimirovna, et al. “Extremely short halogen bond: the nature and energy of iodine–oxygen interactions in crystalline iodic acid.” Mendeleev Communications, vol. 21, no. 5, Sep. 2011, pp. 250-252. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.09.006.

Abstract

The mechanism of the hypercoordination of the iodine atom and its role in the crystal packing of iodic acid were examined within the topological analysis of the experimental electron density function.

References

2.
Halogen Bonding Based Recognition Processes:  A World Parallel to Hydrogen Bonding
Metrangolo P., Neukirch H., Pilati T., Resnati G.
Accounts of Chemical Research, 2005
3.
10.1016/j.mencom.2011.09.006_bib0015
Ritter
Chem. Eng. News, 2009
4.
Systematic Investigation of Halogen Bonding in Protein–Ligand Interactions
Hardegger L.A., Kuhn B., Spinnler B., Anselm L., Ecabert R., Stihle M., Gsell B., Thoma R., Diez J., Benz J., Plancher J., Hartmann G., Banner D.W., Haap W., Diederich F., et. al.
Angewandte Chemie - International Edition, 2010
5.
Halogen bonds in biological molecules
Auffinger P., Hays F.A., Westhof E., Ho P.S.
Proceedings of the National Academy of Sciences of the United States of America, 2004
7.
Competition of Hydrogen Bonds and Halogen Bonds in Complexes of Hypohalous Acids with Nitrogenated Bases
Alkorta I., Blanco F., Solimannejad M., Elguero J.
Journal of Physical Chemistry A, 2008
8.
Halogen bonding: the σ-hole
Clark T., Hennemann M., Murray J.S., Politzer P.
Journal of Molecular Modeling, 2006
10.
The Nature of the Chemical Bond in Linear Three-Body Systems: From I3–to Mixed Chalcogen/Halogen and Trichalcogen Moieties
Aragoni M.C., Arca M., Devillanova F.A., Garau A., Isaia F., Lippolis V., Mancini A.
Bioinorganic Chemistry and Applications, 2007
11.
Halogen Bonding: A Study based on the Electronic Charge Density
Amezaga N.J., Pamies S.C., Peruchena N.M., Sosa G.L.
Journal of Physical Chemistry A, 2009
14.
Ab initio and atoms in molecules analyses of halogen bonding with a continuum of strength
15.
10.1016/j.mencom.2011.09.006_bib0075
Bader
Atoms in Molecules. A Quantum Theory, 1990
17.
About the evaluation of the local kinetic, potential and total energy densities in closed-shell interactions
18.
Unexpected “amphoteric” character of the halogen bond: the charge density study of the co-crystal of N-methylpyrazine iodide with I2
21.
Topological definition of crystal structure: determination of the bonded interactions in solid molecular chlorine
Tsirelson V.G., Zhou P.F., Tang T.-., Bader R.F.
Acta Crystallographica Section A Foundations of Crystallography, 1995
22.
The Surprising Crystal Packing of Chlorinefluoride
Boese R., Boese A.D., Bláser D., Antipin M.Y., Ellern A., Seppelt K.
Angewandte Chemie International Edition in English, 1997
23.
Shishkina A.V., Stash A.I., Civalleri B., Ellern A., Tsirelson V.G.
Mendeleev Communications, 2010
24.
The Crystal Structure of Iodic Acid
Rogers M.T., Helmholz L.
Journal of the American Chemical Society, 1941
25.
Ståhl K., Szafranski M., Junker F., Dalbøge H., Abildgaard F., Led J.J., Christensen S.B.
Acta Chemica Scandinavica, 1992
26.
10.1016/j.mencom.2011.09.006_bib0130
Taouti
Z. Kristallogr., 2008
27.
Intercalation of Iodic Acid into the Layered Uranyl Iodate, UO2(IO3)2(H2O)
28.
γ‐HIO3 – a Metastable, Centrosymmetric Polymorph of Iodic Acid
Fischer A., Lindsjö M.
Zeitschrift fur Anorganische und Allgemeine Chemie, 2005
29.
Nelyubina Y.V., Lyssenko K.A., Kostyanovsky R.G., Bakulin D.A., Antipin M.Y.
Mendeleev Communications, 2008
30.
On the Accuracy of Theoretically and Experimentally Determined Electron Densities of Polar Bonds
Henn J., Ilge D., Leusser D., Stalke D., Engels B.
Journal of Physical Chemistry A, 2004
31.
Anion–anion interactions: their nature, energy and role in crystal formation
Nelyubina Y.V., Antipin M.Y., Lyssenko K.A.
Russian Chemical Reviews, 2010
32.
Experimental and Theoretical Study of the Transannular Intramolecular Interaction and Cage Effect in the Atrane Framework of Boratrane and 1-Methylsilatrane
Korlyukov A.A., Lyssenko K.A., Antipin M.Y., Kirin V.N., Chernyshev E.A., Knyazev S.P.
Inorganic Chemistry, 2002
33.
Molecular Structure of 1-Germatrahol and its Complex With Chloroform
Voronkov M.G., Korlyukov A.A., Zelbst É.A., Knyazev S.P., rsev I.M., Chernyshev E.A., Antipin M.Y.
Journal of Structural Chemistry, 2010
35.
Stereoelectronic Effects in N−C−S and N−N−C Systems: Experimental and ab Initio AIM Study
Bushmarinov I.S., Antipin M.Y., Akhmetova V.R., Nadyrgulova G.R., Lyssenko K.A.
Journal of Physical Chemistry A, 2008
36.
Crystal Structure of IO2F
Minkwitz R., Berkei M., Ludwig R.
Inorganic Chemistry, 2001
37.
Crystal and Molecular Structure of Xenon Trioxide
Templeton D.H., Zalkin A., Forrester J.D., Williamson S.M.
Journal of the American Chemical Society, 1963
38.
Atomic energy in the 'Atoms in Molecules' theory and its use for solving chemical problems
39.
Pseudosymmetry as viewed using charge density analysis
Nelyubina Y.V., Antipin M.Y., Cherepanov I.A., Lyssenko K.A.
CrystEngComm, 2010