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Cucurbituril chemistry: a tale of supramolecular success

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TLDR
Cucurbit[n]urils have become key units in various self-organizing and stimulus-controlled assemblies, as well as in advanced materials and drug carriers.
Abstract
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 pumpkin-shaped macrocycles have been generating some tremendous interest in the supramolecular community. They have also become key units in various self-organizing and stimulus-controlled assemblies, as well as in advanced materials and drug carriers. The scope of this review is limited to the main family of cucurbit[n]urils (n = 5, 6, 7, 8, 10). The reader will find an overview of their preparation, their physicochemical and biological properties, as well as their recognition abilities towards various organic and inorganic guests. Detailed thermodynamic and kinetic considerations, as well as multiple applications including supramolecular catalysis are also discussed.

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Citations
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Journal ArticleDOI

Selective recognition and determination of phenylalanine by a fluorescent probe based on cucurbit[8]uril and palmatine.

TL;DR: 1H NMR spectroscopy reveal that the palmatine can be encapsulated into the cucurbit (Q) in aqueous solution to form stable 1:2 host-guest inclusion complex PAL2@Q [8], which exhibits moderate intensity fluorescence property.
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Porous supramolecular assemblies and functional properties of perhydroxylated cucurbit[6]uril and polyoxometallates

TL;DR: In this paper, perhydroxylated cucurbit[6]uril {(HO)12Q[6]} and Keggin-type polyoxometallates (POMs) such as H3[PMo12O40] and H3 [PW12O 40] were used as basic building blocks, and interaction of POMs in the acidic aqueous solutions yielded two types of supramolecular assemblies.
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Hybrid Molecular Container Based on Glycoluril and Triptycene: Synthesis, Binding Properties, and Triggered Release.

TL;DR: Optical transmittance and TEM measurements provide strong evidence that receptor 1 undergoes co-assemble with amphiphilic guest C10 in water to form supramolecular bilayer vesicles that can encapsulate the hydrophilic anticancer drug doxorubicin and the Hydrophobic dye Nile red.
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New guests for the cucurbit[8]uril host. Formation of G2H ternary complexes†

TL;DR: In this article, three monocationic 4-phenylpyridinium derivatives, namely 1-(hydroxyethyl)-4phenyl-pyrinium (1+) bromide, 1-(octaethyleneglycol)-4-phenylon-polymorphic-polycyclic-cyclic (EP-cyclohexyl)-phenyl pyridine (CPP) derivatives, and 4-[4-(methoxymethoxy)phenyl]pyrithoxy)pyridonium (3+) iodide, were
References
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Journal ArticleDOI

The cucurbit[n]uril family

TL;DR: In 1981, the macrocyclic methylene-bridged glycoluril hexamer (CB[6]) was dubbed "cucurbituril" by Mock and co-workers because of its resemblance to the most prominent member of the cucurbitaceae family of plants--the pumpkin.
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Cucurbituril homologues and derivatives: new opportunities in supramolecular chemistry.

TL;DR: This Account is a compilation of recent literature covering the syntheses of the homologues and derivatives, and their supramolecular chemistry of cucurbituril, a synthetic receptor.
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Nanotechnology in Drug Delivery and Tissue Engineering: From Discovery to Applications

TL;DR: Two important aspects of nanomedicine, drug delivery and tissue engineering are discussed, highlighting the advances the authors have recently experienced, the challenges they are currently facing, and what they are likely to witness in the near future.
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