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Intramolecular Halogen Bonding Supported by an Aryldiyne Linker

https://doi.org/10.1021/jo501015x
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/anie.200800128openalex-snapshot
Halogen Bonding in Supramolecular Chemistry
inferredcites →https://doi.org/10.1002/anie.201006781openalex-snapshot
Systematic Investigation of Halogen Bonding in Protein–Ligand Interactions
inferredcites →https://doi.org/10.1002/chem.201102562openalex-snapshot
Magnitude and Origin of the Attraction and Directionality of the Halogen Bonds of the Complexes of C6F5X and C6H5X (X=I, Br, Cl and F) with Pyridine
inferredcites →https://doi.org/10.1002/chem.201202689openalex-snapshot
Halogen Bonding between Anions and Iodoperfluoroorganics: Solution‐Phase Thermodynamics and Multidentate‐Receptor Design
inferredcites →https://doi.org/10.1002/cphc.201200799openalex-snapshot
Halogen Bonding: An Interim Discussion
inferredcites →https://doi.org/10.1002/ejoc.201201512openalex-snapshot
Alternative Motifs for Halogen Bonding
inferredcites →https://doi.org/10.1002/jcc.1058openalex-snapshot
6‐31G* basis set for third‐row atoms
inferredcites →https://doi.org/10.1002/pro.2201openalex-snapshot
Halogen bonding (X‐bonding): A biological perspective
inferredcites →https://doi.org/10.1007/s00214-007-0310-xopenalex-snapshot
The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other functionals
inferredcites →https://doi.org/10.1007/s00894-011-1015-6openalex-snapshot
Halogen bond tunability I: the effects of aromatic fluorine substitution on the strengths of halogen-bonding interactions involving chlorine, bromine, and iodine
inferredcites →https://doi.org/10.1016/j.cossms.2009.05.001openalex-snapshot
Halogen bonding: Recent advances
inferredcites →https://doi.org/10.1021/ar0400995openalex-snapshot
Halogen Bonding Based Recognition Processes: A World Parallel to Hydrogen Bonding
inferredcites →https://doi.org/10.1021/ar400014ropenalex-snapshot
Synthetic Ion Transporters that Work with Anion−π Interactions, Halogen Bonds, and Anion–Macrodipole Interactions
inferredcites →https://doi.org/10.1021/ar400103ropenalex-snapshot
The Halogen Bond in the Design of Functional Supramolecular Materials: Recent Advances
inferredcites →https://doi.org/10.1021/cg005540mopenalex-snapshot
Crystal Engineering through Halogen Bonding: Complexes of Nitrogen Heterocycles with Organic Iodides
inferredcites →https://doi.org/10.1021/cg020063oopenalex-snapshot
Molecular Graphics: From Science to Art
inferredcites →https://doi.org/10.1021/cg900823dopenalex-snapshot
Halogen-Bonded Cocrystals of 4-(N,N-Dimethylamino)pyridine with Fluorinated Iodobenzenes
inferredcites →https://doi.org/10.1021/ci400539qopenalex-snapshot
Halogen Bond: Its Role beyond Drug–Target Binding Affinity for Drug Discovery and Development
inferredcites →https://doi.org/10.1021/ct300180wopenalex-snapshot
Treatment of Halogen Bonding in the OPLS-AA Force Field: Application to Potent Anti-HIV Agents
inferredcites →https://doi.org/10.1021/ct301064topenalex-snapshot
Halogen Bonds: Benchmarks and Theoretical Analysis
inferredcites →https://doi.org/10.1021/ct8004134openalex-snapshot
Br···O Complexes as Probes of Factors Affecting Halogen Bonding: Interactions of Bromobenzenes and Bromopyrimidines with Acetone
inferredcites →https://doi.org/10.1021/ic010965zopenalex-snapshot
Unique 2:1 Complex with a trans-Chelating Bis-Pyridine Ligand
inferredcites →https://doi.org/10.1021/j100785a001openalex-snapshot
van der Waals Volumes and Radii
inferredcites →https://doi.org/10.1021/ja202096fopenalex-snapshot
Anion Receptors Composed of Hydrogen- and Halogen-Bond Donor Groups: Modulating Selectivity With Combinations of Distinct Noncovalent Interactions
inferredcites →https://doi.org/10.1021/ja9086352openalex-snapshot
Thermodynamics of Halogen Bonding in Solution: Substituent, Structural, and Solvent Effects
inferredcites →https://doi.org/10.1021/ja953281xopenalex-snapshot
The Nature and Geometry of Intermolecular Interactions between Halogens and Oxygen or Nitrogen
inferredcites →https://doi.org/10.1021/jm3012068openalex-snapshot
Principles and Applications of Halogen Bonding in Medicinal Chemistry and Chemical Biology
inferredcites →https://doi.org/10.1021/jo300279mopenalex-snapshot
Correlations between Computation and Experimental Thermodynamics of Halogen Bonding
inferredcites →https://doi.org/10.1021/jp065887lopenalex-snapshot
On the Spectroscopic and Thermochemical Properties of ClO, BrO, IO, and Their Anions
inferredcites →https://doi.org/10.1021/jp8107182openalex-snapshot
Experimental and Theoretical Study of the Br···N Halogen Bond in Complexes of 1,4-Dibromotetrafluorobenzene with Dipyridyl Derivatives
inferredcites →https://doi.org/10.1021/ol302586mopenalex-snapshot
Palladacycle-Catalyzed Reaction of Bicyclic Alkenes with Terminal Ynones: Regiospecific Synthesis of Polysubstituted Furans
inferredcites →https://doi.org/10.1039/b803329nopenalex-snapshot
Halogen bonded supramolecular complexes and networks
inferredcites →https://doi.org/10.1039/b926326hopenalex-snapshot
Nonbonding interactions of organic halogens in biological systems: implications for drug discovery and biomolecular design
inferredcites →https://doi.org/10.1039/c0py00013bopenalex-snapshot
Controlled room temperature ROP of L-lactide by ICl3: a simple halogen-bonding catalyst
inferredcites →https://doi.org/10.1039/c2ce26150bopenalex-snapshot
Halogen bonding at work: recent applications in synthetic chemistry and materials science
inferredcites →https://doi.org/10.1039/c2cs15292dopenalex-snapshot
Halogen bonding in solution
inferredcites →https://doi.org/10.1039/c3cp00054kopenalex-snapshot
Halogen bonding and other σ-hole interactions: a perspective
inferredcites →https://doi.org/10.1039/c3cp52768aopenalex-snapshot
The relative roles of electrostatics and dispersion in the stabilization of halogen bonds
inferredcites →https://doi.org/10.1055/s-0033-1338981openalex-snapshot
Multidentate Halogen-Bond Donors as Lewis Acidic Activators or Catalysts in Halide Abstraction Reactions
inferredcites →https://doi.org/10.1071/ch10259openalex-snapshot
Directional Weak Intermolecular Interactions: σ-Hole Bonding
inferredcites →https://doi.org/10.1073/pnas.0407607101openalex-snapshot
Halogen bonds in biological molecules
inferredcites →https://doi.org/10.1107/s0108767307043930openalex-snapshot
A short history of SHELX
inferredcites →https://doi.org/10.1126/science.1162215openalex-snapshot
Halogen Versus Hydrogen
inferredcites →https://doi.org/10.1126/science.1168679openalex-snapshot
Nonporous Organic Solids Capable of Dynamically Resolving Mixtures of Diiodoperfluoroalkanes
inferredcites →https://doi.org/10.1351/pac-rec-12-05-10openalex-snapshot
Definition of the halogen bond (IUPAC Recommendations 2013)

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4647246openalex-extracted
Light-Switchable N-Alkylation Using Amine-Functionalized Mof
inferred← citeshttps://doi.org/10.1002/0471264180.or116.01openalex-snapshot
A Half Century of the Sonogashira Reaction
inferred← citeshttps://doi.org/10.1002/9783527825738.ch1openalex-snapshot
Halogen Bonding: An Introduction
inferred← citeshttps://doi.org/10.1002/9783527825738.ch2openalex-snapshot
Thermodynamics of Halogen Bonding in Solution
inferred← citeshttps://doi.org/10.1002/chem.201900924openalex-snapshot
Benchmarking of Halogen Bond Strength in Solution with Nickel Fluorides: Bromine versus Iodine and Perfluoroaryl versus Perfluoroalkyl Donors
inferred← citeshttps://doi.org/10.1002/chem.202001706openalex-snapshot
Halogen‐Bonded Assemblies of Arylene Imides and Diimides: Insight from Electronic, Structural, and Computational Studies
inferred← citeshttps://doi.org/10.1002/cphc.201901001openalex-snapshot
Halogen and Chalcogen Bond Energies Evaluated Using Electron Density Properties
inferred← citeshttps://doi.org/10.1002/ejoc.201403671openalex-snapshot
Intramolecular Halogen Bonding in Solution: 15N, 13C, and 19F NMR Studies of Temperature and Solvent Effects
inferred← citeshttps://doi.org/10.1002/ejoc.201700969openalex-snapshot
Comparing Strong and Weak Halogen Bonding in Solution: 13C NMR, UV/Vis, Crystallographic, and Computational Studies of an Intramolecular Model
inferred← citeshttps://doi.org/10.1007/s00214-015-1796-2openalex-snapshot
Intramolecular halogen bonding: an interacting quantum atoms study
inferred← citeshttps://doi.org/10.1007/s11224-015-0671-zopenalex-snapshot
Intramolecular halogen bonds in 1,2-aryldiyne molecules: a theoretical study
inferred← citeshttps://doi.org/10.1016/b978-0-323-90891-7.00001-3openalex-snapshot
Recent advances on halogen bonds within the quantum theory of atoms-in-molecules
inferred← citeshttps://doi.org/10.1016/j.apcatb.2024.123924openalex-snapshot
Light-Switchable N-Alkylation Using Amine-Functionalized MOF
inferred← citeshttps://doi.org/10.1016/j.comptc.2014.09.004openalex-snapshot
Halogen–halogen interactions in perhalogenated ethanes: An interacting quantum atoms study
inferred← citeshttps://doi.org/10.1016/j.dyepig.2018.06.022openalex-snapshot
Pnicogen, halogen and hydrogen bonds in (E)-1-(2,2-dichloro-1-(2-nitrophenyl)vinyl)-2-(para-substituted phenyl)-diazenes
inferred← citeshttps://doi.org/10.1016/j.nexres.2024.100127openalex-snapshot
Deciphering the role of noncovalent interactions in the conformational preferences of Bis(3-Chlorobenzyl) imidazolium salt: Perspective for Cox-2 selective anti-inflammatory activity
inferred← citeshttps://doi.org/10.1021/acs.cgd.0c00205openalex-snapshot
Halogen Bonds (N---I) at Work: Supramolecular Catemeric Architectures of 2,7-Dipyridylfluorene with ortho -, meta -, or para -Diiodotetrafluorobenzene Isomers
inferred← citeshttps://doi.org/10.1021/acs.cgd.3c01325openalex-snapshot
Halogen-Bonded Supramolecular Parallelograms: From Self-Complementary Iodoalkyne Halogen-Bonded Dimers to 1:1 and 2:2 Iodoalkyne Halogen-Bonded Cocrystals
inferred← citeshttps://doi.org/10.1021/acs.cgd.4c00228openalex-snapshot
Definition of the Halogen Bond (IUPAC Recommendations 2013): A Revisit
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.0c01177openalex-snapshot
Coordination of a Central Atom by Multiple Intramolecular Pnicogen Bonds
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01064openalex-snapshot
Effects of Halogen and Hydrogen Bonding on the Electronics of a Conjugated Rotor
inferred← citeshttps://doi.org/10.1021/acsomega.3c09696openalex-snapshot
Molecular Insights into Water–Chloride and Water–Water Interactions in the Supramolecular Architecture of Aconine Hydrochloride Dihydrate
inferred← citeshttps://doi.org/10.1021/acsorginorgau.6c00009openalex-snapshot
Exploring the Competition between Halogen Bonding and CH Hydrogen Bonding in Bromoarenes Using an Aryldiyne Template
inferred← citeshttps://doi.org/10.1021/cg5014076openalex-snapshot
The Power of Nonconventional Phenyl C–H···N Hydrogen Bonds: Supportive Crystal-Packing Force and Dominant Supramolecular Engineering Force
inferred← citeshttps://doi.org/10.1039/bk9781782621737-00530openalex-snapshot
Intramolecular Beryllium Bonds. Further Insights into Resonance Assistance Phenomena
inferred← citeshttps://doi.org/10.1039/c5cp03625aopenalex-snapshot
Do resonance-assisted intramolecular halogen bonds exist without a charge transfer and a σ-hole?
inferred← citeshttps://doi.org/10.1039/c6cc02535hopenalex-snapshot
“Conformational lock” via unusual intramolecular C–F⋯OC and C–H⋯Cl–C parallel dipoles observed in in situ cryocrystallized liquids
inferred← citeshttps://doi.org/10.1039/c7ce00060jopenalex-snapshot
Impact of the complementary electronic nature of C–X and M–X halogens and intramolecular X⋯O interaction on supramolecular assemblies of Zn( ii ) complexes of o-halophenyl substituted hydrazides
inferred← citeshttps://doi.org/10.1039/c8nj00759dopenalex-snapshot
Halogen-bond driven self-assembly of triangular macrocycles
inferred← citeshttps://doi.org/10.1039/c9ce01449gopenalex-snapshot
Halogen bonding (HaB) in E–I⋯X–M systems: influence of the halogen donor on the HaB nature
inferred← citeshttps://doi.org/10.1039/d0qo01139hopenalex-snapshot
N -(2,3,5,6-Tetrafluoropyridyl)sulfoximines: synthesis, X-ray crystallography, and halogen bonding
inferred← citeshttps://doi.org/10.1039/d1tc02420eopenalex-snapshot
Stimuli-responsive luminescent supramolecular assemblies and co-assemblies through orthogonal dipole–dipole interactions and halogen bonding
inferred← citeshttps://doi.org/10.1039/d4ce01053aopenalex-snapshot
Complexes of N -chloroquinuclidinium with chloride: strong halogen bonding via chlorine atoms
inferred← citeshttps://doi.org/10.1055/s-0039-1691743openalex-snapshot
Convenient Synthesis of Furo[3,2-b]quinolin-4(1H)-ones
inferred← citeshttps://doi.org/10.1093/bib/bbaf347openalex-snapshot
Impact of halogenation on scaffold toxicity assessed using HD-GEM machine learning model
inferred← citeshttps://doi.org/10.1107/s2052252525001447openalex-snapshot
The origin of synthons and supramolecular motifs: beyond atoms and functional groups
inferred← citeshttps://doi.org/10.1107/s2056989024010995openalex-snapshot
Intra- and intermolecular C—H...F hydrogen bonds in the crystal structure of 1,2-bis[2-(2,3,4,5-tetrafluorophenyl)ethynyl]benzene
inferred← citeshttps://doi.org/10.3390/molecules30030639openalex-snapshot
Halogen Bonding and Rearrangements in Complexes of N-Chlorosuccinimide with Halides
inferred← citeshttps://doi.org/10.70675/6db9605dz94faz4a13zaeadz746ed472e7fdopenalex-snapshot
Nouveaux outils pour l'analyse de liaisons chimiques remarquables : caractérisation théorique de la nature des liens avec le béryllium
inferred← citeshttps://doi.org/10.70675/f3cfb875z65ccz42bfz9c1az39371ac550b1openalex-snapshot
Molecular organization in solid-state using sigma-hole interactions : Exploring the effect of crystalline environment
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