Scinovex
articleTop 1% cited

Cucurbituril Homologues and Derivatives:  New Opportunities in Supramolecular Chemistry

Accounts of Chemical Research · 2003 · Vol. 36(8) · pp. 621–630
Jae Wook LeeS. SamalNarayanan SelvapalamHee‐Joon KimKimoon Kim

Abstract

The supramolecular chemistry of cucurbituril, a synthetic receptor, is fascinating because of the remarkable guest binding behavior of the host. Studies in the field, however, have met with limitations, since the only species known was the hexameric macrocyclic compound, cucurbit[6]uril. Recently we synthesized its homologues, cucurbit[n]uril (n = 5, 7, 8), and derivatives. These new members of the cucurbituril family have expanded the scope further, and interest in them has grown enormously. This Account is a compilation of recent literature covering the syntheses of the homologues and derivatives, and their supramolecular chemistry.

Supramolecular Chemistry and ComplexesBoron Compounds in ChemistryCrystallography and molecular interactionsCucurbiturilSupramolecular chemistryChemistryHost–guest chemistryCombinatorial chemistryScope (computer science)NanotechnologyOrganic chemistryMoleculeMaterials science
Citations
1,795
FWCI
27.73
field-weighted impact
References
25
Percentile
100%
vs. same field & year
Citations per year
Cited by
Pillararenes: Versatile Synthetic Receptors for Supramolecular Chemistry
European Journal of Organic Chemistry · 2013 · 253 citations
Pillararenes, A New Class of Macrocycles for Supramolecular Chemistry
Accounts of Chemical Research · 2012 · 1,411 citations
The Cucurbit[<i>n</i>]uril Family
Angewandte Chemie International Edition · 2005 · 2,402 citations
References
Artificial Molecular Machines
Angewandte Chemie International Edition · 2000 · 2,469 citations
Related articles
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.