1 : 1 and 2 : 1 co-crystals of alkoxystilbazoles with tetrafluoroiodobenzenes: halogen bonding, a rare Carene–H⋯N hydrogen bond and unsymmetric iodine⋯pyridine interactions

CrystEngComm ◽  
2013 ◽  
Vol 15 (44) ◽  
pp. 8947 ◽  
Author(s):  
Carsten Präsang ◽  
Linda J. McAllister ◽  
Adrian C. Whitwood ◽  
Duncan W. Bruce
Keyword(s):  
Hydrogen Bond ◽  
Halogen Bonding

Halogen Bonding Organocatalysis Enhanced through Intramolecular Hydrogen Bonds

2022 ◽  
Author(s):  
Asia Marie S Riel ◽  
Daniel Adam Decato ◽  
Jiyu Sun ◽  
Orion Berryman
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonds ◽  
Halogen Bond ◽  
Direct Interaction ◽  
Halogen Bonding ◽  
Intramolecular Hydrogen Bonds ◽  
Intramolecular Hydrogen

Recent results indicate a halogen bond donor is strengthened through direct interaction with a hydrogen bond to the electron-rich belt of the halogen. Here, this Hydrogen Bond enhanced Halogen Bond...

The15N NMR chemical shift in the characterization of weak halogen bonding in solution

2017 ◽  
Vol 203 ◽  
pp. 333-346 ◽  
Author(s):  
Sebastiaan B. Hakkert ◽  
Jürgen Gräfenstein ◽  
Mate Erdelyi
Keyword(s):  
Hydrogen Bond ◽  
Chemical Shift ◽  
Halogen Bond ◽  
Molar Fraction ◽  
Halogen Bonding ◽  
Relative Strength ◽  
Lewis Base ◽  
Halogen Bonds ◽  
Bonded Complexes

We have studied the applicability of15N NMR spectroscopy in the characterization of the very weak halogen bonds of nonfluorinated halogen bond donors with a nitrogenous Lewis base in solution. The ability of the technique to detect the relative strength of iodine-, bromine- and chlorine-centered halogen bonds, as well as solvent and substituent effects was evaluated. Whereas computations on the DFT level indicate that15N NMR chemical shifts reflect the diamagnetic deshielding associated with the formation of a weak halogen bond, the experimentally observed chemical shift differences were on the edge of detectability due to the low molar fraction of halogen-bonded complexes in solution. The formation of the analogous yet stronger hydrogen bond of phenols have induced approximately ten times larger chemical shift changes, and could be detected and correlated to the electronic properties of substituents of the hydrogen bond donors. Overall,15N NMR is shown to be a suitable tool for the characterization of comparably strong secondary interactions in solution, but not sufficiently accurate for the detection of the formation of thermodynamically labile, weak halogen bonded complexes.

scholarly journals Halogen-Bonding-Driven Self-Assembly of Solvates of Tetrabromoterephthalic Acid

Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 198
Author(s):  
Nucharee Chongboriboon ◽  
Kodchakorn Samakun ◽  
Winya Dungkaew ◽  
Filip Kielar ◽  
Mongkol Sukwattanasinitt ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonding ◽  
Phase Transitions ◽  
Self Assembly ◽  
Solid Phase ◽  
Halogen Bond ◽  
Halogen Bonding ◽  
Cooperative Effect ◽  
Hydrogen Bonding Interactions ◽  
Solvent Molecules

Halogen bonding is one of the most interesting noncovalent attractions capable of self-assembly and recognition processes in both solution and solid phase. In this contribution, we report on the formation of two solvates of tetrabromoterephthalic acid (H2Br4tp) with acetonitrile (MeCN) and methanol (MeOH) viz. H2Br4tp·2MeCN (1MeCN) and H2Br4tp·2MeOH (2MeOH). The host structures of both 1MeCN and 2MeOH are assembled via the occurrence of simultaneous Br···Br, Br···O, and Br···π halogen bonding interactions, existing between the H2Br4tp molecular tectons. Among them, the cooperative effect of the dominant halogen bond in combination with hydrogen bonding interactions gave rise to different supramolecular assemblies, whereas the strength of the halogen bond depends on the type of hydrogen bond between the molecules of H2Br4tp and the solvents. These materials show a reversible release/resorption of solvent molecules accompanied by evident crystallographic phase transitions.

Halogen bonding directed supramolecular assembly in bromo-substituted trezimides and tennimides

CrystEngComm ◽  
2014 ◽  
Vol 16 (10) ◽  
pp. 1893-1903 ◽  
Author(s):  
Pavle Mocilac ◽  
John F. Gallagher
Keyword(s):  
Hydrogen Bond ◽  
Solid State ◽  
Crystal Structures ◽  
Supramolecular Assembly ◽  
Halogen Bonding ◽  
Strong Hydrogen Bond ◽  
Aggregation Process ◽  
Halogen Bonds ◽  
State Aggregation ◽  
Hydrogen Bond Donors

The imide-based trezimide and tennimide macrocycle crystal structures typically aggregate as 1-D chains through C–Br⋯OC/N/π(arene) halogen bonds (withNc≤ 0.90) that dominate the solid-state aggregation process in the absence of classical strong hydrogen bond donors.

Competition between hydrogen and halogen bonding in the structures of 5,10-dihydroxy-5,10-dihydroboranthrenes

2014 ◽  
Vol 70 (1) ◽  
pp. 157-171 ◽  
Author(s):  
Krzysztof Durka ◽  
Sergiusz Luliński ◽  
Katarzyna N. Jarzembska ◽  
Jaromir Smętek ◽  
Janusz Serwatowski ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Density Functional ◽  
Crystal Packing ◽  
Halogen Bond ◽  
Halogen Bonding ◽  
Structural Diversity ◽  
Interesting Case ◽  
Molecular Arrangement ◽  
Supramolecular Arrangements

X-ray crystallographic and computational studies are reported for a series of boranthrenes, substituted with halogen atoms. The role of competitive hydrogen (O—H...O, O—H...F, C—H...O) and halogen (Cl...Cl, O...Br, F...F) bonding interactions on the molecular arrangement in the crystal structures is discussed. The structural analysis and calculations reveal that the O—H...O hydrogen bond in the unsubstituted derivative 5,10-dihydroxy-5,10-dihydroboranthrene, C12H10B2O2, is of moderate strength (ca−20 kJ mol−1), but weaker than that in the related thiophene derivative 4,8-dihydro-4,8-dihydroxy-p-diborino[2,3-b:5,6-b]dithiophene, C8H6B2O2S2(ca−40 kJ mol−1). This is due to shielding of the OH group by the H atoms in the β-position of the boranthrene unit. Structural diversity derived from the flexibility of the O—H...O hydrogen bond facilitates the occurrence of other competitive interactions. For instance, in the 1,6-difluoro derivative, C12H8B2F2O2, the crystal packing results from O—H...F and F...F interactions. In turn, the 1,6-dibromo derivative, C12H8B2Br2O2, is dominated by Br...O halogen-bond interactions. In the most interesting case, the 1,6-dichloro derivative, C12H8B2Cl2O2, molecular disorder leads to the formation of two different supramolecular arrangements co-existing in the crystal lattice, one based on the Cl...Cl and C—H...O bonds, and the other stabilized by O—H...O hydrogen bonds. Calculations performed with density-functional theory (DFT;CRYSTAL09) andPIXELmethodologies show that both lattices are characterized by similar energy values (ca−100 kJ mol−1). A mixed arrangement with random or short-range-ordered molecular orientations can also be expected.

scholarly journals Supramolecular hierarchy among halogen and hydrogen bond donors in light-induced surface patterning

2015 ◽  
Vol 3 (4) ◽  
pp. 759-768 ◽  
Author(s):  
Marco Saccone ◽  
Valentina Dichiarante ◽  
Alessandra Forni ◽  
Alexis Goulet-Hanssens ◽  
Gabriella Cavallo ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Halogen Bonding ◽  
Surface Patterning ◽  
Supramolecular Polymers ◽  
Hydrogen Bond Donors

Halogen bonding is an interaction of choice in supramolecular polymers for efficient light-induced surface patterning.

scholarly journals Selective perrhenate recognition in pure water by halogen bonding and hydrogen bonding alpha-cyclodextrin based receptors

2017 ◽  
Vol 53 (27) ◽  
pp. 3866-3869 ◽  
Author(s):  
Stuart P. Cornes ◽  
Mark R. Sambrook ◽  
Paul D. Beer
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonding ◽  
Pure Water ◽  
Aqueous Media ◽  
Halogen Bonding ◽  
Anion Receptors ◽  
Hydrogen Bond Donor

Alpha-cyclodextrin based anion receptors containing halogen and hydrogen bond donor motifs display selective association of perrhenate in neutral aqueous media.

scholarly journals Synthesis, structure and reactivity of a terminal magnesium fluoride compound, [TpBut,Me]MgF: hydrogen bonding, halogen bonding and C–F bond formation

2016 ◽  
Vol 7 (1) ◽  
pp. 142-149 ◽  
Author(s):  
Michael Rauch ◽  
Serge Ruccolo ◽  
John Paul Mester ◽  
Yi Rong ◽  
Gerard Parkin
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonding ◽  
Halogen Bond ◽  
Bond Formation ◽  
Halogen Bonding ◽  
Magnesium Fluoride ◽  
Fluoride Compound

The terminal magnesium fluoride compound, [TpBut,Me]MgF, serves as a hydrogen bond and halogen bond acceptor for indole and C6F5I, and also reacts with Ph3CCl to form a C–F bond.

Competition between the hydrogen bond and the halogen bond in a [CH3OH–CCl4] complex: a matrix isolation IR spectroscopy and computational study

2020 ◽  
Vol 22 (39) ◽  
pp. 22465-22476
Author(s):  
Dhritabrata Pal ◽  
Sumit Kumar Agrawal ◽  
Amrita Chakraborty ◽  
Shamik Chakraborty
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonding ◽  
Ir Spectroscopy ◽  
Computational Study ◽  
Halogen Bond ◽  
Matrix Isolation ◽  
Halogen Bonding ◽  
Bond Interaction ◽  
Bonding Interaction ◽  
Polar Mixtures

Halogen bonding interaction (X-Bond) is prevalent over hydrogen bonding (H-Bond) interaction in [CH3OH–CCl4] mixtures/clusters: consequence in polar/non-polar mixtures and/or corresponding complexes in atmosphere needs to be investigated.

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