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New Cucurbituril Homologues: Syntheses, Isolation, Characterization, and X-ray Crystal Structures of Cucurbit[ n ]uril ( n = 5, 7, and 8)
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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/(sici)1521-3773(19980202)37:1/2<78::aid-anie78>3.0.co;2-9openalex-snapshot
A Molecular Bowl with Metal Ion as Bottom: Reversible Inclusion of Organic Molecules in Cesium Ion Complexed Cucurbituril
inferredcites →https://doi.org/10.1002/(sici)1521-401x(199901)27:1<38::aid-aheh38>3.0.co;2-uopenalex-snapshot
Effects of Alkali and Alkaline-earth Cations on the Removal of Reactive Dyes with Cucurbituril
inferredcites →https://doi.org/10.1002/jlac.19053390102openalex-snapshot
I. Ueber Condensationsproducte aus Glycoluril und Formaldehyd
inferredcites →https://doi.org/10.1016/s0032-3861(98)00354-1openalex-snapshot
Polyrotaxanes and pseudopolyrotaxanes of polyamides and cucurbituril 1Dedicated to Professor Hartwig Höcker on occasion of his 60th birthday. 1
inferredcites →https://doi.org/10.1021/ja00189a053openalex-snapshot
Dynamics of molecular recognition involving cucurbituril
inferredcites →https://doi.org/10.1021/ja00222a031openalex-snapshot
Organic ligand-receptor interactions between cucurbituril and alkylammonium ions
inferredcites →https://doi.org/10.1021/ja961551lopenalex-snapshot
Self-Assembly of a Polyrotaxane Containing a Cyclic “Bead” in Every Structural Unit in the Solid State: Cucurbituril Molecules Threaded on a One-Dimensional Coordination Polymer
inferredcites →https://doi.org/10.1021/ja962071xopenalex-snapshot
Molecular Container Assembly Capable of Controlling Binding and Release of Its Guest Molecules: Reversible Encapsulation of Organic Molecules in Sodium Ion Complexed Cucurbituril
inferredcites →https://doi.org/10.1021/ja963096zopenalex-snapshot
Polycatenated Two-Dimensional Polyrotaxane Net
inferredcites →https://doi.org/10.1021/ja980029ropenalex-snapshot
Molecular Necklace: Quantitative Self-Assembly of a Cyclic Oligorotaxane from Nine Molecules
inferredcites →https://doi.org/10.1021/jo00168a069openalex-snapshot
Host-guest binding capacity of cucurbituril
inferredcites →https://doi.org/10.1021/jo00168a070openalex-snapshot
Cycloaddition induced by cucurbituril. A case of Pauling principle catalysis
inferredcites →https://doi.org/10.1021/jo00373a018openalex-snapshot
Structure and selectivity in host-guest complexes of cucurbituril
inferredcites →https://doi.org/10.1039/a704574copenalex-snapshot
Helical polyrotaxane: cucurbituril ‘beads’ threaded onto a helical one-dimensional coordination polymer
inferredcites →https://doi.org/10.1039/a902990gopenalex-snapshot
Catalytically self-threading polyrotaxanes
inferredcites →https://doi.org/10.1246/cl.1996.503openalex-snapshot
A Simple Construction of a Rotaxane and Pseudorotaxane: Syntheses and X-Ray Crystal Structures of Cucurbituril Threaded on Substituted Spermine
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Host-Guest Complexes between Molnupiravir Drug and Cucurbit[n = 5–9]Urils: A DFT Investigation
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Cucurbiturils, Synthesis and Applications
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A Three-Dimensional Polyrotaxane Network
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A Two-Dimensional Polyrotaxane with Large Cavities and Channels: A Novel Approach to Metal-Organic Open-Frameworks by Using Supramolecular Building Blocks
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Novel Pseudorotaxane-Terminated Dendrimers: Supramolecular Modification of Dendrimer Periphery
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Selective Inclusion of a Hetero-Guest Pair in a Molecular Host: Formation of Stable Charge-Transfer Complexes in Cucurbit[8]uril
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Macrocycles within Macrocycles: Cyclen, Cyclam, and Their Transition Metal Complexes Encapsulated in Cucurbit[8]uril
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Zwei Mechanismen für die langsame Wirt-Gast-Komplexierung zwischen Cucurbit[6]uril und Cyclohexylmethylamin: pH-abhängige supramolekulare Kinetik
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Cucurbit[n]uril Derivatives Soluble in Water and Organic Solvents
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Polarisierbarkeiten im Inneren von molekularen Containern
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A Cucurbituril-Based Gyroscane: A New Supramolecular Form
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Von molekularen Gyroskopen, Matroschka-Puppen und anderem „Nano-Spielzeug“
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A Two-Dimensional Polyrotaxane with Large Cavities and Channels: A Novel Approach to Metal-Organic Open-Frameworks by Using Supramolecular Building Blocks
inferred← citeshttps://doi.org/10.1002/1521-3773(20010216)40:4<746::aid-anie7460>3.0.co;2-popenalex-snapshot
Novel Pseudorotaxane-Terminated Dendrimers: Supramolecular Modification of Dendrimer Periphery
inferred← citeshttps://doi.org/10.1002/1521-3773(20010417)40:8<1526::aid-anie1526>3.0.co;2-topenalex-snapshot
Selective Inclusion of a Hetero-Guest Pair in a Molecular Host: Formation of Stable Charge-Transfer Complexes in Cucurbit
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Macrocycles within Macrocycles: Cyclen, Cyclam, and Their Transition Metal Complexes Encapsulated in Cucurbit[8]uril
inferred← citeshttps://doi.org/10.1002/1521-3773(20010903)40:17<3155::aid-anie3155>3.0.co;2-7openalex-snapshot
Two Mechanisms of Slow Host-Guest Complexation between Cucurbit[6]uril and Cyclohexylmethylamine: pH-Responsive Supramolecular Kinetics
inferred← citeshttps://doi.org/10.1002/1521-3773(20011119)40:22<4233::aid-anie4233>3.0.co;2-dopenalex-snapshot
Cucurbit[n]uril Derivatives Soluble in Water and Organic Solvents
inferred← citeshttps://doi.org/10.1002/1521-3773(20020118)41:2<275::aid-anie275>3.0.co;2-mopenalex-snapshot
A Cucurbituril-Based Gyroscane: A New Supramolecular Form This research was supported by the Australian Research Council and the University of New South Wales. G.R.L. acknowledges the award of a Royal Society Fellowship tenable in Australia.
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Of Molecular Gyroscopes, Matroshka Dolls, and Other “Nano”-Toys
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Molecular Encapsulation of Redox‐Active Guests
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Templating Photoreactions in Solution
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Complexation of Fluorescent Dyes by Macrocyclic Hosts
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Supramolecular Redox Transduction: Macrocyclic Receptors for Organic Guests
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Appendix A: Glossary of Terminology
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The Fundamentals of Making Mechanical Bonds
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A Short History of the Mechanical Bond
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Cyclic Host Liquids for the Formation of Rotaxanes and Their Applications
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inferred← citeshttps://doi.org/10.1002/anie.200250214openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200250692openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200351925openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200461806openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200463071openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200500502openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200603149openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200702189openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200705346openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200705591openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200800581openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200802805openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201005317openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201300404openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201305061openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201309635openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201400718openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201600911openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201602116openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201708971openalex-snapshot
Supramolecular Radical Anions Triggered by Bacteria In Situ for Selective Photothermal Therapy
inferred← citeshttps://doi.org/10.1002/anie.201805884openalex-snapshot
Applications of Pillar[n]arene‐Based Supramolecular Assemblies
inferred← citeshttps://doi.org/10.1002/anie.201806575openalex-snapshot
Cucurbit[8]uril (CB[8])‐Based Supramolecular Switches
inferred← citeshttps://doi.org/10.1002/anie.201901882openalex-snapshot
Efficient Room‐Temperature Phosphorescence of a Solid‐State Supramolecule Enhanced by Cucurbit[6]uril
inferred← citeshttps://doi.org/10.1002/anie.201913055openalex-snapshot
Tiara[5]arenes: Synthesis, Solid‐State Conformational Studies, Host–Guest Properties, and Application as Nonporous Adaptive Crystals
inferred← citeshttps://doi.org/10.1002/anie.202002666openalex-snapshot
Cucurbit[ n ]uril‐Based Supramolecular Frameworks Assembled through Outer‐Surface Interactions
inferred← citeshttps://doi.org/10.1002/anie.202014399openalex-snapshot
Guest Exchange by a Partial Energy Ratchet in Water
inferred← citeshttps://doi.org/10.1002/anie.202206763openalex-snapshot
Cucurbituril‐Based Supramolecular Polymers for Biomedical Applications
inferred← citeshttps://doi.org/10.1002/anie.202218706openalex-snapshot
Smart Materials Based on Synthetic Host Molecules: The Role of Host–Guest Chemistry in the Fabrication and Application
inferred← citeshttps://doi.org/10.1002/anie.202313864openalex-snapshot
Stabilization of Guest Molecules inside Cation‐Lidded Cucurbiturils Reveals that Hydration of Receptor Sites Can Impede Binding
inferred← citeshttps://doi.org/10.1002/anie.202417384openalex-snapshot
Engineering Single Ni Sites on 3D Cage‐like Cucurbit[n]uril Ligands for Efficient and Selective CO 2 Photocatalytic Reduction
inferred← citeshttps://doi.org/10.1002/anie.202421108openalex-snapshot
2,3 : 6,7‐Naphthalenediimide‐Based Chiral Triangular Macrocycle: Self‐Assembled Helix, Outer π‐Surface Directed Co‐Assembly and Circularly Polarized Luminescence
inferred← citeshttps://doi.org/10.1002/anie.202505713openalex-snapshot
Thermodynamics of Water Displacement from Binding Sites and its Contributions to Supramolecular and Biomolecular Affinity
inferred← citeshttps://doi.org/10.1002/anie.4944487openalex-snapshot
Spiro[16]arene: A Spirocycle‐Bridged Macrocycle With Nanocarbon Recognition
inferred← citeshttps://doi.org/10.1002/anie.7480690openalex-snapshot
Stiffness Reinforcement in Polymer Networks Through Supramolecular Topological Linking
inferred← citeshttps://doi.org/10.1002/anse.202400025openalex-snapshot
Unimolecular Cucurbit[7]uril‐Based Indicator Displacement Assay with Dual Signal‐Readout for the Detection of Drugs
inferred← citeshttps://doi.org/10.1002/app.57797openalex-snapshot
Direct Cross‐Linking of Cucurbit[7]uril Pseudopolyrotaxanes to Prepare Slide‐Ring Hydrogels
inferred← citeshttps://doi.org/10.1002/asia.200700043openalex-snapshot
Toward High‐Generation Rotaxane Dendrimers That Incorporate a Ring Component on Every Branch: Noncovalent Synthesis of a Dendritic [10]Pseudorotaxane with 13 Molecular Components
inferred← citeshttps://doi.org/10.1002/asia.200800054openalex-snapshot
Synthetic Molecular Machine Based on Reversible End‐to‐Interior and End‐to‐End Loop Formation Triggered by Electrochemical Stimuli
inferred← citeshttps://doi.org/10.1002/asia.200900510openalex-snapshot
Binding Studies on CB[6] with a Series of 1‐Alkyl‐3‐methylimidazolium Ionic Liquids in an Aqueous System
inferred← citeshttps://doi.org/10.1002/asia.201000388openalex-snapshot
Inclusion of Carboxyl Function Inside of Cucurbiturils and its Use in Molecular Switches
inferred← citeshttps://doi.org/10.1002/asia.201000665openalex-snapshot
U‐Shaped Conformation of Alkyl Chains Bound to a Synthetic Receptor Cucurbit[8]uril
inferred← citeshttps://doi.org/10.1002/asia.201500003openalex-snapshot
Coordination of Alkaline Earth Metal Ions in the Inverted Cucurbit[7]uril Supramolecular Assemblies Formed in the Presence of [ZnCl4]2− and [CdCl4]2−
inferred← citeshttps://doi.org/10.1002/asia.201600875openalex-snapshot
Surface‐Bound Cucurbit[8]uril Catenanes on Magnetic Nanoparticles Exhibiting Molecular Recognition
inferred← citeshttps://doi.org/10.1002/asia.201601411openalex-snapshot
Stimuli‐Responsive Cucurbit[7]uril‐Mediated BSA Nanoassembly for Uptake and Release of Doxorubicin
inferred← citeshttps://doi.org/10.1002/asia.201601670openalex-snapshot
Differences between the Interactions of Linear and Tetrahedron‐like Ditopic Guests with Cucurbit[8]uril: Steric Hindrance and Molecular Structure Play Dominant Roles
inferred← citeshttps://doi.org/10.1002/asia.201700386openalex-snapshot
Self‐Healable Supramolecular Hydrogel Formed by Nor‐Seco‐Cucurbit[10]uril as a Supramolecular Crosslinker
inferred← citeshttps://doi.org/10.1002/asia.201801498openalex-snapshot
A Study of the Interaction Between Cucurbit[8]uril and Alkyl‐Substituted 4‐Pyrrolidinopyridinium Salts
inferred← citeshttps://doi.org/10.1002/asia.202001224openalex-snapshot
Adaptive Se‐Te Metathesis Controlled by Cucurbituril‐Based Host‐Guest Interaction
inferred← citeshttps://doi.org/10.1002/cctc.202402125openalex-snapshot
Catalysis in Chemical Modification of Proteins
inferred← citeshttps://doi.org/10.1002/chem.200390008openalex-snapshot
Guest Binding and Orientation within Open Nanoscale Hosts
inferred← citeshttps://doi.org/10.1002/chem.200500917openalex-snapshot
Supramolecular Assembly of 2,7‐Dimethyldiazapyrenium and Cucurbit[8]uril: A New Fluorescent Host for Detection of Catechol and Dopamine
inferred← citeshttps://doi.org/10.1002/chem.200601830openalex-snapshot
Nitroxide Radicals as Probes for Exploring the Binding Properties of the Cucurbit[7]uril Host
inferred← citeshttps://doi.org/10.1002/chem.200700199openalex-snapshot
Cucurbit[8]uril/Cucurbit[7]uril Controlled Off/On Fluorescence of the Acridizinium and 9‐Aminoacridizinium Cations in Aqueous Solution
inferred← citeshttps://doi.org/10.1002/chem.200700402openalex-snapshot
Inclusion Complexation of Diquat and Paraquat by the Hosts Cucurbit[7]uril and Cucurbit[8]uril
inferred← citeshttps://doi.org/10.1002/chem.200702003openalex-snapshot
pH‐Triggered Dethreading–Rethreading and Switching of Cucurbit[6]uril on Bistable [3]Pseudorotaxanes and [3]Rotaxanes
inferred← citeshttps://doi.org/10.1002/chem.200800398openalex-snapshot
Supramolecular Complexation of N‐Alkyl‐ and N,N′‐Dialkylpiperazines with Cucurbit[6]uril in Aqueous Solution and in the Solid State
inferred← citeshttps://doi.org/10.1002/chem.200800463openalex-snapshot
Supramolecular Tandem Enzyme Assays for Multiparameter Sensor Arrays and Enantiomeric Excess Determination of Amino Acids
inferred← citeshttps://doi.org/10.1002/chem.200900305openalex-snapshot
Complexation of Aliphatic Ammonium Ions with a Water‐Soluble Cucurbit[6]uril Derivative in Pure Water: Isothermal Calorimetric, NMR, and X‐ray Crystallographic Study
inferred← citeshttps://doi.org/10.1002/chem.200901504openalex-snapshot
Sequence‐Specific Self‐Sorting of the Binding Sites of a Ditopic Guest by Cucurbituril Homologues and Subsequent Formation of a Hetero[4]pseudorotaxane
inferred← citeshttps://doi.org/10.1002/chem.200901522openalex-snapshot
Cucurbit[7]uril Complexation Drives Thermal trans – cis ‐Azobenzene Isomerization and Enables Colorimetric Amine Detection
inferred← citeshttps://doi.org/10.1002/chem.201001194openalex-snapshot
Inclusion of a Nitronyl Nitroxyl Radical and Its Hydrochloride in Cucurbit[8]uril
inferred← citeshttps://doi.org/10.1002/chem.201002274openalex-snapshot
Benzobis(imidazolium)–Cucurbit[8]uril Complexes for Binding and Sensing Aromatic Compounds in Aqueous Solution
inferred← citeshttps://doi.org/10.1002/chem.201002618openalex-snapshot
Isolated Supramolecular [Ru(bpy)3]–Viologen–[Ru(bpy)3] Complexes with Trapped CB[7,8] and Photoinduced Electron‐Transfer Study in Nonaqueous Solution
inferred← citeshttps://doi.org/10.1002/chem.201101611openalex-snapshot
Host‐Enhanced π–π Interaction for Water‐Soluble Supramolecular Polymerization
inferred← citeshttps://doi.org/10.1002/chem.201102675openalex-snapshot
A Facile Synthesis of Dynamic Supramolecular Aggregates of Cucurbit[n]uril (n=5–8) Capped with Gold Nanoparticles in Aqueous Media
inferred← citeshttps://doi.org/10.1002/chem.201103049openalex-snapshot
Evidence of Higher Complexes Between Cucurbit[7]uril and Cationic Surfactants
inferred← citeshttps://doi.org/10.1002/chem.201103434openalex-snapshot
Bistable Cucurbituril Rotaxanes Without Stoppers
inferred← citeshttps://doi.org/10.1002/chem.201202083openalex-snapshot
From Containers to Catalysts: Supramolecular Catalysis within Cucurbiturils
inferred← citeshttps://doi.org/10.1002/chem.201202378openalex-snapshot
Chiral Supramolecular Switches Based on (R)‐Binaphthalene–Bipyridinium Guests and Cucurbituril Hosts
inferred← citeshttps://doi.org/10.1002/chem.201204097openalex-snapshot
Asararenes—A Family of Large Aromatic Macrocycles
inferred← citeshttps://doi.org/10.1002/chem.201301703openalex-snapshot
Crystalline Hybrid Solid Materials of Palladium and Decamethylcucurbit[5]uril as Recoverable Precatalysts for Heck Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/chem.201400039openalex-snapshot
Synthesis and Electronic Properties of 1,2‐Hemisquarimines and Their Encapsulation in a Cucurbit[7]uril Host
inferred← citeshttps://doi.org/10.1002/chem.201402821openalex-snapshot
Light Control of Stoichiometry and Motion in Pseudorotaxanes Comprising a Cucurbit[7]uril Wheel and an Azobenzene‐Bipyridinium Axle
inferred← citeshttps://doi.org/10.1002/chem.201501353openalex-snapshot
Rotaxanes Capped with Host Molecules: Supramolecular Behavior of Adamantylated Bisimidazolium Salts Containing a Biphenyl Centerpiece
inferred← citeshttps://doi.org/10.1002/chem.201502461openalex-snapshot
Supramolecular Protein Immobilization on Lipid Bilayers
inferred← citeshttps://doi.org/10.1002/chem.201503194openalex-snapshot
Supracolloidal Architectures Self‐Assembled in Microdroplets
inferred← citeshttps://doi.org/10.1002/chem.201600877openalex-snapshot
Supramolecular Antibiotic Switches: A Potential Strategy for Combating Drug Resistance
inferred← citeshttps://doi.org/10.1002/chem.201601796openalex-snapshot
Glycoluril‐Derived Molecular Clips are Potent and Selective Receptors for Cationic Dyes in Water
inferred← citeshttps://doi.org/10.1002/chem.201602810openalex-snapshot
How Does Solvation Affect the Binding of Hydrophilic Amino Saccharides to Cucurbit[7]uril with Exceptional Anomeric Selectivity?
inferred← citeshttps://doi.org/10.1002/chem.201604149openalex-snapshot
From Packed “Sandwich” to “Russian Doll”: Assembly by Charge‐Transfer Interactions in Cucurbit[10]uril
inferred← citeshttps://doi.org/10.1002/chem.201605045openalex-snapshot
Outer Surface Interactions of Cucurbit[6]uril That Trigger the Assembly of Supramolecular Three‐Dimensional Polycatenanes
inferred← citeshttps://doi.org/10.1002/chem.201605284openalex-snapshot
Assessment of Cooperativity in Ternary Peptide‐Cucurbit[8]uril Complexes
inferred← citeshttps://doi.org/10.1002/chem.201605394openalex-snapshot
Complexation of Racemic 2,6‐Helic[6]arene and Its Hexamethyl‐Substituted Derivative with Quaternary Ammonium Salts, N‐Heterocyclic Salts, and Tetracyanoquinodimethane
inferred← citeshttps://doi.org/10.1002/chem.201701275openalex-snapshot
DESolution of CD and CB Macrocycles
inferred← citeshttps://doi.org/10.1002/chem.201800856openalex-snapshot
Directional Self‐Sorting with Cucurbit[8]uril Controlled by Allosteric π–π and Metal–Metal Interactions
inferred← citeshttps://doi.org/10.1002/chem.201802981openalex-snapshot
Hybrid Molecular Container Based on Glycoluril and Triptycene: Synthesis, Binding Properties, and Triggered Release
inferred← citeshttps://doi.org/10.1002/chem.201901037openalex-snapshot
A Selective Cucurbit[8]uril‐Peptide Beacon Ensemble for the Ratiometric Fluorescence Detection of Peptides
inferred← citeshttps://doi.org/10.1002/chem.201902057openalex-snapshot
A Cucurbit[8]uril 2:2 Complex with a Negative pKa Shift
inferred← citeshttps://doi.org/10.1002/chem.201904443openalex-snapshot
Dual‐Stimuli Responsive 2D Supramolecular Organic Framework for the Detection of Azoreductase Activity
inferred← citeshttps://doi.org/10.1002/chem.202003897openalex-snapshot
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