On the public citation graph
Anion Recognition and Binding Constant Determination
0 signed · 68 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9783527644131.ch2openalex-snapshot
Quantitative Analysis of Binding Properties
inferredcites →https://doi.org/10.1002/adsc.201700986openalex-snapshot
A Case Study of Thiourea‐Assisted Iminium Formation by Hydroxyl Anion Binding: Kinetic, Spectroscopic and Computational Evidences
inferredcites →https://doi.org/10.1002/anie.200704717openalex-snapshot
Pure CH Hydrogen Bonding to Chloride Ions: A Preorganized and Rigid Macrocyclic Receptor
inferredcites →https://doi.org/10.1002/anie.201206881openalex-snapshot
Hydrogen‐Bond‐Mediated Supramolecular Iminium Ion Catalysis
inferredcites →https://doi.org/10.1002/anie.201305496openalex-snapshot
Chiral Silanediols in Anion‐Binding Catalysis
inferredcites →https://doi.org/10.1002/anie.201307133openalex-snapshot
Thiophosphoramide‐Based Cooperative Catalysts for Brønsted Acid Promoted Ionic Diels–Alder Reactions
inferredcites →https://doi.org/10.1002/anie.201404570openalex-snapshot
Rhodium‐Catalyzed Asymmetric Hydrogenation of Unprotected NH Imines Assisted by a Thiourea
inferredcites →https://doi.org/10.1002/anie.201406786openalex-snapshot
Rationally Designed Multifunctional Supramolecular Iminium Catalysis: Direct Vinylogous Michael Addition of Unmodified Linear Dienol Substrates
inferredcites →https://doi.org/10.1002/anie.201611019openalex-snapshot
Catalysis with Chalcogen Bonds
inferredcites →https://doi.org/10.1002/anie.201913054openalex-snapshot
Stereodivergent Anion Binding Catalysis with Molecular Motors
inferredcites →https://doi.org/10.1002/cber.18940270364openalex-snapshot
Einfluss der Configuration auf die Wirkung der Enzyme
inferredcites →https://doi.org/10.1002/chem.201002340openalex-snapshot
Aromatic and Aliphatic CH Hydrogen Bonds Fight for Chloride while Competing Alongside Ion Pairing within Triazolophanes
inferredcites →https://doi.org/10.1002/chem.201203360openalex-snapshot
“Click” Bis‐Triazoles as Neutral CH⋅⋅⋅Anion‐Acceptor Organocatalysts
inferredcites →https://doi.org/10.1002/chem.201700845openalex-snapshot
Stereoselective and Enantiospecific Mono‐ and Bis‐C−H Azidation of Tröger Bases: Insight on Bridgehead Iminium Intermediates and Application to Anion‐Binding Catalysis
inferredcites →https://doi.org/10.1002/chem.201701763openalex-snapshot
Ion Pairing and Co‐facial Stacking Drive High‐Fidelity Bisulfate Assembly with Cyanostar Macrocyclic Hosts
inferredcites →https://doi.org/10.1002/chem.201900119openalex-snapshot
Highly Enantio‐ and Diastereoselective Catalytic Asymmetric Tamura Cycloaddition Reactions
inferredcites →https://doi.org/10.1006/abio.1995.9984openalex-snapshot
Nuclear Magnetic Resonance as a Tool for Determining Protonation Constants of Natural Polyprotic Bases in Solution
inferredcites →https://doi.org/10.1007/978-3-642-15444-7openalex-snapshot
Anion Recognition in Supramolecular Chemistry
inferredcites →https://doi.org/10.1007/s00216-003-2020-0openalex-snapshot
Determination of protonation constants of some fluorinated polyamines by means of 13 C NMR data processed by the new computer program HypNMR2000. Protonation sequence in polyamines
inferredcites →https://doi.org/10.1016/j.chempr.2017.08.003openalex-snapshot
Anion Binding in Solution: Beyond the Electrostatic Regime
inferredcites →https://doi.org/10.1016/s0010-8545(98)00260-4openalex-snapshot
Hyperquad simulation and speciation (HySS): a utility program for the investigation of equilibria involving soluble and partially soluble species
inferredcites →https://doi.org/10.1021/acs.orglett.8b00855openalex-snapshot
Pyrrole-Based Anion-Responsive π-Electronic Molecules as Hydrogen-Bonding Catalysts
inferredcites →https://doi.org/10.1021/acs.orglett.8b03778openalex-snapshot
Convergent Ditopic Receptors Enhance Anion Binding upon Alkali Metal Complexation for Catalyzing the Ritter Reaction
inferredcites →https://doi.org/10.1021/acscatal.6b01384openalex-snapshot
Anion-Abstraction Catalysis: The Cooperative Mechanism of α-Chloroether Activation by Dual Hydrogen-Bond Donors
inferredcites →https://doi.org/10.1021/ed079p944openalex-snapshot
Holleman-Wiberg's Inorganic Chemistry (edited by Wiberg, Nils)
inferredcites →https://doi.org/10.1021/ja01002a035openalex-snapshot
Cyclic polyethers and their complexes with metal salts
inferredcites →https://doi.org/10.1021/ja064012hopenalex-snapshot
Calix[4]pyrrole as a Chloride Anion Receptor: Solvent and Countercation Effects
inferredcites →https://doi.org/10.1021/ja1102844openalex-snapshot
Chiral 1,2,3-Triazoliums as New Cationic Organic Catalysts with Anion-Recognition Ability: Application to Asymmetric Alkylation of Oxindoles
inferredcites →https://doi.org/10.1021/ja2119207openalex-snapshot
Isothermal Calorimetric Titrations on Charge-Assisted Halogen Bonds: Role of Entropy, Counterions, Solvent, and Temperature
inferredcites →https://doi.org/10.1021/ja3028668openalex-snapshot
Catalytic Asymmetric Ring Openings of Meso and Terminal Aziridines with Halides Mediated by Chiral 1,2,3-Triazolium Silicates
inferredcites →https://doi.org/10.1021/ja4013276openalex-snapshot
Transmembrane Halogen-Bonding Cascades
inferredcites →https://doi.org/10.1021/ja500125ropenalex-snapshot
An Overlooked yet Ubiquitous Fluoride Congenitor: Binding Bifluoride in Triazolophanes Using Computer-Aided Design
inferredcites →https://doi.org/10.1021/ja803341yopenalex-snapshot
Strong, Size-Selective, and Electronically Tunable C−H···Halide Binding with Steric Control over Aggregation from Synthetically Modular, Shape-Persistent [3 4 ]Triazolophanes
inferredcites →https://doi.org/10.1021/ja9756331openalex-snapshot
An Introduction to Hydrogen Bonding By George A. Jeffrey (University of Pittsburgh). Oxford University Press: New York and Oxford. 1997. ix + 303 pp. $60.00. ISBN 0-19-509549-9.
inferredcites →https://doi.org/10.1021/jacs.5b00190openalex-snapshot
A Dual-Catalysis Anion-Binding Approach to the Kinetic Resolution of Amines: Insights into the Mechanism via a Combined Experimental and Computational Study
inferredcites →https://doi.org/10.1021/jacs.5b05839openalex-snapshot
Electrostatic and Allosteric Cooperativity in Ion-Pair Binding: A Quantitative and Coupled Experiment–Theory Study with Aryl–Triazole–Ether Macrocycles
inferredcites →https://doi.org/10.1021/jacs.5b07863openalex-snapshot
Cationic Multidentate Halogen-Bond Donors in Halide Abstraction Organocatalysis: Catalyst Optimization by Preorganization
inferredcites →https://doi.org/10.1021/jacs.6b04686openalex-snapshot
On- and Off-Cycle Catalyst Cooperativity in Anion-Binding Catalysis
inferredcites →https://doi.org/10.1021/jacs.6b07501openalex-snapshot
Hydrogen-Bonded Homoleptic Fluoride–Diarylurea Complexes: Structure, Reactivity, and Coordinating Power
inferredcites →https://doi.org/10.1021/jacs.7b02329openalex-snapshot
A Bis-calix[4]pyrrole Enzyme Mimic That Constrains Two Oxoanions in Close Proximity
inferredcites →https://doi.org/10.1021/jacs.7b04955openalex-snapshot
Switching between Anion-Binding Catalysis and Aminocatalysis with a Rotaxane Dual-Function Catalyst
inferredcites →https://doi.org/10.1021/jacs.7b05832openalex-snapshot
Reductive Etherification via Anion-Binding Catalysis
inferredcites →https://doi.org/10.1021/jacs.8b05915openalex-snapshot
Supramolecular Regulation of Anions Enhances Conductivity and Transference Number of Lithium in Liquid Electrolytes
inferredcites →https://doi.org/10.1021/jacs.8b10538openalex-snapshot
Allosteric Control of Photofoldamers for Selecting between Anion Regulation and Double-to-Single Helix Switching
inferredcites →https://doi.org/10.1021/jacs.9b01885openalex-snapshot
Discovery and Elucidation of Counteranion Dependence in Photoredox Catalysis
inferredcites →https://doi.org/10.1021/jo0016273openalex-snapshot
Conformational Features and Anion-Binding Properties of Calix[4]pyrrole: A Theoretical Study
inferredcites →https://doi.org/10.1021/ol1005856openalex-snapshot
Intramolecular Hydrogen Bonds Preorganize an Aryl-triazole Receptor into a Crescent for Chloride Binding
inferredcites →https://doi.org/10.1038/nchem.1668openalex-snapshot
A pentagonal cyanostar macrocycle with cyanostilbene CH donors binds anions and forms dialkylphosphate [3]rotaxanes
inferredcites →https://doi.org/10.1039/c0cs00062kopenalex-snapshot
Determining association constants from titration experiments in supramolecular chemistry
inferredcites →https://doi.org/10.1039/c2cc17459fopenalex-snapshot
Shape persistence delivers lock-and-key chloride binding in triazolophanes
inferredcites →https://doi.org/10.1039/c3cc46858eopenalex-snapshot
Synergistic Lewis base and anion-binding catalysis for the enantioselective vinylogous addition of deconjugated butenolides to allenoates
inferredcites →https://doi.org/10.1039/c4cs00157eopenalex-snapshot
Calix[4]pyrroles: versatile molecular containers with ion transport, recognition, and molecular switching functions
inferredcites →https://doi.org/10.1039/c6cc03888copenalex-snapshot
The death of the Job plot, transparency, open science and online tools, uncertainty estimation methods and other developments in supramolecular chemistry data analysis
inferredcites →https://doi.org/10.1039/c7nj04660jopenalex-snapshot
Hydrogen-bonding cyclodiphosphazanes: superior effects of 3,5-(CF 3 ) 2 -substitution in anion-recognition and counter-ion catalysis
inferredcites →https://doi.org/10.1039/c7sc05290aopenalex-snapshot
Phosphate–phosphate oligomerization drives higher order co-assemblies with stacks of cyanostar macrocycles
inferredcites →https://doi.org/10.1080/10610270802527051openalex-snapshot
Modelling triazolophane–halide binding equilibria using Sivvu analysis of UV–vis titration data recorded under medium binding conditions
inferredcites →https://doi.org/10.1126/science.aaw5145openalex-snapshot
Chloride capture using a C–H hydrogen-bonding cage
inferredcites →https://doi.org/10.3891/acta.chem.scand.38b-0885openalex-snapshot
Solvent Properties of Dichloromethane. III. Conductivity Studies of some Tetraalkylammonium-, Tetraphenylarsonium- and Bis(triphenylphosphine)iminium Salts in Dichloromethane.
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.4799544openalex-extracted
Novel Fac-Rei(Co)3 Based Perrhenate (Reviio4-) Bridged Mixed Valence Octanuclear Rectangular Rhenacycle
inferred← citeshttps://doi.org/10.1002/ange.202409070openalex-snapshot
Cone Angles Quantify and Predict the Affinity and Reactivity of Anion Complexes between Trifluoroborates and Rigid Macrocycles
inferred← citeshttps://doi.org/10.1002/anie.202409070openalex-snapshot
Cone Angles Quantify and Predict the Affinity and Reactivity of Anion Complexes between Trifluoroborates and Rigid Macrocycles
inferred← citeshttps://doi.org/10.1002/chem.202301613openalex-snapshot
Chiroptical Recognition of Carboxylates with Charge‐Neutral Double‐Stranded Zinc(II) Helicates
inferred← citeshttps://doi.org/10.1002/chem.202302339openalex-snapshot
Solvent Acts as the Referee in a Match‐Up Between Charged and Preorganized Receptors
inferred← citeshttps://doi.org/10.1016/j.ica.2024.122250openalex-snapshot
Novel fac-ReI(CO)3 based perrhenate (ReVIIO4−) bridged mixed valence octanuclear rectangular rhenacycle
inferred← citeshttps://doi.org/10.1021/jacs.2c08579openalex-snapshot
A Charge-Neutral Self-Assembled L2Zn2 Helicate as Bench-Stable Receptor for Anion Recognition at Nanomolar Concentration
inferred← citeshttps://doi.org/10.1039/d3py01354eopenalex-snapshot
Pillar[5]arene-based dually crosslinked supramolecular gel as a sensor for the detection of adiponitrile
inferred← citeshttps://doi.org/10.1039/d5sc01329aopenalex-snapshot
Expanding the toolbox for supramolecular chemistry: probing host–guest interactions and binding with in situ FTIR spectroscopy
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.