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Journal ArticleDOI

Modes of binding interaction between viologen guests and the cucurbit[7]uril host.

Kwangyul Moon, +1 more
- 22 Jan 2004 - 
- Vol. 6, Iss: 2, pp 185-188
TLDR
A new pseudorotaxane was designed and synthesized on the basis of viologen-CB7 binding interactions and its mode of interaction is different with longer chain viologens due to the favorable hydrophobic interactions between the terminal alkyl substituents and the inner cavity of the host.
About
This article is published in Organic Letters.The article was published on 2004-01-22. It has received 210 citations till now. The article focuses on the topics: Viologen.

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Citations
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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.
Journal ArticleDOI

Cucurbituril chemistry: a tale of supramolecular success

TL;DR: Cucurbit[n]urils have become key units in various self-organizing and stimulus-controlled assemblies, as well as in advanced materials and drug carriers.
Journal ArticleDOI

Supramolecular Chemistry in Water

TL;DR: An overview of recent advances in the area of water-soluble synthetic receptors as well as self-assembly and molecular recognition in water is offered, through consideration of the functionalities that are used to increase the water solubility.
Journal ArticleDOI

Mechanised nanoparticles for drug delivery

TL;DR: This review serves to highlight the evolution of surface-functionalisation of SNPs with supermolecules and also with MIMs, the mechanisms through which controlled-release of cargo from mechanised SNPs occurs, and the results from the in vitro application of these mechanisation SNPs.
Journal ArticleDOI

Mechanism of host-guest complexation by cucurbituril.

TL;DR: The factors affecting host-guest complexation between the molecular container compound cucurbit[6]uril (CB6) and various guests in aqueous solution are studied, and a detailed complexation mechanism in the presence of cations is derived.
References
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Journal ArticleDOI

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.
Journal ArticleDOI

Inclusion of methylviologen in cucurbit[7]uril

TL;DR: The electrochemical study reveals that unlike β-cyclodextrin, CB[7] prefers the charged species, MV dication, and cation radical (MV+⋅) to the fully reduced neutral species as guests.
Journal ArticleDOI

Cucurbit[7]uril: A Very Effective Host for Viologens and Their Cation Radicals

TL;DR: The rate of the heterogeneous electron-transfer reaction between the complexed viologen dication and cation radical remained fast in the voltammetric time scale and the binding constants were measured.
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