Collect. Czech. Chem. Commun.
2001, 66, 1375-1379
https://doi.org/10.1135/cccc20011375
Charge Distribution Within 1,2-Dicarba-closo-dodecaborane: Dipole Moments of Its Phenyl Derivatives
Drahomír Hnyka,*, Václav Všetečkab, Ladislav Drožb and Otto Exnerc
a Institute of Inorganic Chemistry, Academy of Sciences of the Czech Republic, CZ-250 68 Řež, Czech Republic
b Department of Organic Chemistry, Charles University, Hlavova 2030, CZ-128 40 Prague 2, Czech Republic
c Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, CZ-166 10 Prague 6, Czech Republic
Crossref Cited-by Linking
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- Melichar Petr, Hnyk Drahomír, Fanfrlík Jindřich: A systematic examination of classical and multi-center bonding in heteroborane clusters. Phys. Chem. Chem. Phys. 2018, 20, 4666. <https://doi.org/10.1039/C7CP07422K>
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- Fanfrlík Jindřich, Hnyk Drahomír: Dihalogen and Pnictogen Bonding in Crystalline Icosahedral Phosphaboranes. Crystals 2018, 8, 390. <https://doi.org/10.3390/cryst8100390>
- Fanfrlík Jindřich, Pecina Adam, Řezáč Jan, Sedlak Robert, Hnyk Drahomír, Lepšík Martin, Hobza Pavel: B–H⋯π: a nonclassical hydrogen bond or dispersion contact?. Phys. Chem. Chem. Phys. 2017, 19, 18194. <https://doi.org/10.1039/C7CP02762A>
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- Fanfrlík Jindřich, Hnyk Drahomír: Chalcogens act as inner and outer heteroatoms in borane cages with possible consequences for σ-hole interactions. CrystEngComm 2016, 18, 8982. <https://doi.org/10.1039/C6CE01861K>
- Vishnevskiy Yury V., Tikhonov Denis S., Reuter Christian G., Mitzel Norbert W., Hnyk Drahomír, Holub Josef, Wann Derek A., Lane Paul D., Berger Raphael J. F., Hayes Stuart A.: Influence of Antipodally Coupled Iodine and Carbon Atoms on the Cage Structure of 9,12-I2-closo-1,2-C2B10H10: An Electron Diffraction and Computational Study. Inorg. Chem. 2015, 54, 11868. <https://doi.org/10.1021/acs.inorgchem.5b02102>
- Campanelli Anna Rita, Domenicano Aldo, Hnyk Drahomír: Transmission of Electronic Substituent Effects across the 1,12-Dicarba-closo-dodecaborane Cage: A Computational Study Based on Structural Variation, Atomic Charges, and 13C NMR Chemical Shifts. J. Phys. Chem. A 2015, 119, 205. <https://doi.org/10.1021/jp5106407>
- Pecina Adam, Lepšík Martin, Hnyk Drahomír, Hobza Pavel, Fanfrlík Jindřich: Chalcogen and Pnicogen Bonds in Complexes of Neutral Icosahedral and Bicapped Square-Antiprismatic Heteroboranes. J. Phys. Chem. A 2015, 119, 1388. <https://doi.org/10.1021/jp511101n>
- Nunes João Pedro F., Holub Josef, Rankin David W. H., Wann Derek A., Hnyk Drahomír: A computational analysis of the apparent nido vs. hypho conflict: are we dealing with six- or eight-vertex open-face diheteroboranes?. Dalton Trans. 2015, 44, 11819. <https://doi.org/10.1039/C5DT01460C>
- Hnyk Drahomír, Holub Josef, Růžička Aleš, Padělková Zdeňka, Bühl Michael: Expanding the structural chemistry of the weakly coordinating closo-carborane CB11H12 −: its monoiodo derivatives with and without C 5v symmetry. Struct Chem 2013, 24, 927. <https://doi.org/10.1007/s11224-013-0246-9>
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- Hnyk Drahomír, Všetečka Václav, Drož Ladislav: Charge distribution within hypercarbon-halogenated 1-Ph-2-X-1,2-dicarba-closo-dodecaboranes, (X = F, Cl, Br, I): A dipole moment and computational study. Journal of Molecular Structure 2010, 978, 246. <https://doi.org/10.1016/j.molstruc.2010.02.027>
- Hnyk Drahomír, Holub Josef, Jelínek Tomáš, Macháček Jan, Londesborough Michael G. S.: Revisiting B20H16 by means of a joint computational/experimental NMR approach. Collect. Czech. Chem. Commun. 2010, 75, 1115. <https://doi.org/10.1135/cccc2010073>
- Drož Ladislav, Fox Mark A., Hnyk Drahomír, Low Paul J., MacBride J. A. Hugh, Všetečka Václav: Experimental and computed dipole moments in donor–bridge–acceptor systems with p-phenylene and p-carboranediyl bridges. Collect. Czech. Chem. Commun. 2009, 74, 131. <https://doi.org/10.1135/cccc2008154>
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- Alekseyeva Elena S., Fox Mark A., Howard Judith A. K., Hugh MacBride J. A., Wade Kenneth: Synthesis and crystal structure of an assembly of three ortho‐carborane cages linked via para‐phenylene units: effect of aryl orientation on cage CC bond lengths in C‐aryl‐ortho‐carboranes. Applied Organom Chemis 2003, 17, 499. <https://doi.org/10.1002/aoc.467>