Crystallographic Implications for the Design of Halogen Bonding Anion Receptors

2011 ◽  
Vol 11 (10) ◽  
pp. 4565-4571 ◽  
Author(s):  
Nathan L. Kilah ◽  
Matthew D. Wise ◽  
Paul D. Beer
Keyword(s):  
Halogen Bonding ◽  
Anion Receptors

Halogen bonding-enhanced electrochemical halide anion sensing by redox-active ferrocene receptors

2015 ◽  
Vol 51 (78) ◽  
pp. 14640-14643 ◽  
Author(s):  
Jason Y. C. Lim ◽  
Matthew J. Cunningham ◽  
Jason J. Davis ◽  
Paul D. Beer
Keyword(s):  
Hydrogen Bonding ◽  
Halogen Bonding ◽  
Anion Receptors ◽  
Halide Anion ◽  
Anion Sensing ◽  
Redox Active

The first redox-active halogen bonding anion receptors display larger electrochemical voltammetric responses to halide binding compared to their hydrogen bonding analogues.

scholarly journals Neutral iodotriazole foldamers as tetradentate halogen bonding anion receptors

2017 ◽  
Vol 53 (16) ◽  
pp. 2483-2486 ◽  
Author(s):  
Arseni Borissov ◽  
Jason Y. C. Lim ◽  
Asha Brown ◽  
Kirsten E. Christensen ◽  
Amber L. Thompson ◽  
...  
Keyword(s):  
Halogen Bond ◽  
Anion Recognition ◽  
Halogen Bonding ◽  
Chiral Discrimination ◽  
Anion Receptors

A tetradentate halogen bond donor foldamer receptor framework is shown to exhibit enhanced anion recognition and chiral discrimination properties.

scholarly journals Halogen bonding tetraphenylethene anion receptors: anion‐induced emissive aggregates and photoswitchable recognition

2021 ◽  
Author(s):  
Andrew Docker ◽  
Xiaobo Shang ◽  
Daohe Yuan ◽  
Heike Kuhn ◽  
Zongyao Zhang ◽  
...  
Keyword(s):  
Halogen Bonding ◽  
Anion Receptors

scholarly journals Novel hydrogen- and halogen-bonding anion receptors based on 3-iodopyridinium units

RSC Advances ◽  
2016 ◽  
Vol 6 (72) ◽  
pp. 67540-67549 ◽  
Author(s):  
Valeria Amendola ◽  
Greta Bergamaschi ◽  
Massimo Boiocchi ◽  
Nadia Fusco ◽  
Mario Vincenzo La Rocca ◽  
...  
Keyword(s):  
Synergistic Effect ◽  
Halogen Bonding ◽  
Anion Receptors ◽  
Anionic Species

Iodopyridinium-based tripodal receptors strongly bind anionic species in their bowl-shaped cavity through the synergistic effect of hydrogen- and halogen-bonding interactions.

Anion Receptors Based on Halogen Bonding with Halo-1,2,3-triazoliums

2015 ◽  
Vol 80 (6) ◽  
pp. 3139-3150 ◽  
Author(s):  
Ronny Tepper ◽  
Benjamin Schulze ◽  
Michael Jäger ◽  
Christian Friebe ◽  
Daniel H. Scharf ◽  
...  
Keyword(s):  
Halogen Bonding ◽  
Anion Receptors

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 Halogen bonding tetraphenylethene anion receptors: anion‐induced emissive aggregates and photoswitchable recognition

2021 ◽  
Author(s):  
Andrew Docker ◽  
Xiaobo Shang ◽  
Daohe Yuan ◽  
Heike Kuhn ◽  
Zongyao Zhang ◽  
...  
Keyword(s):  
Halogen Bonding ◽  
Anion Receptors

Structure and energetics of gas phase halogen-bonding in mono-, bi-, and tri-dentate anion receptors as studied by BIRD

2013 ◽  
Vol 15 (20) ◽  
pp. 7638 ◽  
Author(s):  
Elizabeth A. L. Gillis ◽  
Maria Demireva ◽  
Mohammed G. Sarwar ◽  
Michael G. Chudzinski ◽  
Mark S. Taylor ◽  
...  
Keyword(s):  
Gas Phase ◽  
Halogen Bonding ◽  
Anion Receptors

The X40x10 Halogen Bonding Benchmark Revisited: Surprising Importance of (n-1)d Subvalence Correlation

2017 ◽  
Author(s):  
Manoj Kumar Kesharwani ◽  
Nitai Sylvetsky ◽  
Debashree Manna ◽  
Jan M.L. Martin
Keyword(s):  
Dissociation Energy ◽  
Noncovalent Interactions ◽  
Halogen Bonding ◽  
Coupled Cluster ◽  
Dissociation Energies ◽  
Iodine Species ◽  
Explicitly Correlated ◽  
High Level ◽  
Cluster Methods ◽  
Small Separation

<p>We have re-evaluated the X40x10 benchmark for halogen bonding using conventional and explicitly correlated coupled cluster methods. For the aromatic dimers at small separation, improved CCSD(T)–MP2 “high-level corrections” (HLCs) cause substantial reductions in the dissociation energy. For the bromine and iodine species, (n-1)d subvalence correlation increases dissociation energies, and turns out to be more important for noncovalent interactions than is generally realized. As in previous studies, we find that the most efficient way to obtain HLCs is to combine (T) from conventional CCSD(T) calculations with explicitly correlated CCSD-F12–MP2-F12 differences.</p>

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