Cucurbituril-based molecular recognition
The product of the condensation reaction between glycoluril and formaldehyde was first
reported in a thesis by Eberhard Meyer in 1904 (1) and then published by Behrend and co …
reported in a thesis by Eberhard Meyer in 1904 (1) and then published by Behrend and co …
Fluorescent dyes and their supramolecular host/guest complexes with macrocycles in aqueous solution
The fluorescence of organic molecules depends sensitively on their environment.
Fluorescent dyes have accordingly become popular molecular probes not only to determine …
Fluorescent dyes have accordingly become popular molecular probes not only to determine …
Cucurbituril chemistry: a tale of supramolecular success
This review highlights the past six year advances in the blossoming field of cucurbit [n] uril
chemistry. Because of their exceptional recognition properties in aqueous medium, these …
chemistry. Because of their exceptional recognition properties in aqueous medium, these …
Deep inside cucurbiturils: physical properties and volumes of their inner cavity determine the hydrophobic driving force for host–guest complexation
WM Nau, M Florea, KI Assaf - Israel Journal of Chemistry, 2011 - Wiley Online Library
Abstract Cucurbit [n] urils (CBn) bind guest molecules through a combination of electrostatic
interactions with the carbonyl rims and hydrophobic interactions with the inner cavity …
interactions with the carbonyl rims and hydrophobic interactions with the inner cavity …
[PDF][PDF] Supramolecular peptide amphiphile vesicles through host–guest complexation
Single-tail peptide amphiphiles, have been explored as a new class of biomaterials in many
fields including nanotechnology and tissue engineering.[1–3] A typical peptide amphiphile …
fields including nanotechnology and tissue engineering.[1–3] A typical peptide amphiphile …
Substrate-selective supramolecular tandem assays: monitoring enzyme inhibition of arginase and diamine oxidase by fluorescent dye displacement from calixarene …
A combination of moderately selective host− guest binding with the impressive specificity of
enzymatic transformations allows the real-time monitoring of enzymatic reactions in a …
enzymatic transformations allows the real-time monitoring of enzymatic reactions in a …
Role of intramolecular and intermolecular hydrogen bonding in both singlet and triplet excited states of aminofluorenones on internal conversion, intersystem crossing …
GJ Zhao, KL Han - The Journal of Physical Chemistry A, 2009 - ACS Publications
Time-dependent density functional theory method was performed to investigate the
intramolecular and intermolecular hydrogen bonding in both the singlet and triplet electronic …
intramolecular and intermolecular hydrogen bonding in both the singlet and triplet electronic …
Chemical Sensors Based on Cucurbit[n]uril Macrocycles
S Sinn, F Biedermann - Israel Journal of Chemistry, 2018 - Wiley Online Library
Abstract Cucurbit [n] urils (CBn) are glycoluril‐based macrocyclic hosts that bind many
biologically, medicinally and environmentally relevant analytes with record high affinities in …
biologically, medicinally and environmentally relevant analytes with record high affinities in …
Supramolecular encapsulation of benzimidazole-derived drugs by cucurbit [7] uril
UV–vis and NMR spectroscopic techniques were employed to demonstrate the ability of the
synthetic macrocyclic host cucurbit [7] uril (CB7) to solubilize and stabilize widely used …
synthetic macrocyclic host cucurbit [7] uril (CB7) to solubilize and stabilize widely used …
Hydrophobe challenge: A joint experimental and computational study on the host–guest binding of hydrocarbons to cucurbiturils, allowing explicit evaluation of guest …
KI Assaf, M Florea, J Antony… - The Journal of …, 2017 - ACS Publications
The host–guest complexation of hydrocarbons (22 guest molecules) with cucurbit [7] uril was
investigated in aqueous solution using the indicator displacement strategy. The binding …
investigated in aqueous solution using the indicator displacement strategy. The binding …