2008
DOI: 10.3390/s8095313
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Extended Calix[4]arene-Based Receptors for Molecular Recognition and Sensing

Abstract: Recent advances in the area of recognition and sensing have shown that artificial receptors derived from extended calix[4]arenes bearing multiple π-conjugated fluorophoric or chromophoric systems have found useful to enhance binding affinity, selectivity and sensitivity for recognition and sensing of a targeted ion or molecule. A comprehensive review of various π-conjugation-extended calix[4]arene-based receptors with the highlight on the design and binding characterization for recognition and sensing is prese… Show more

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Cited by 54 publications
(18 citation statements)
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“…Protocols for replacing the tbutyl group of the upper rim (R = t-Bu) in the parent calixarenes, which is a necessary blocking group during the base-catalyzed condensation of the phenol and formaldehyde, are also well developed. The variability in n, R, and the phenol substituent provides a rich class of hosts with diverse applications, including sensing [104][105][106]. Although a variety of different-sized resorcinarenes have been reported (n = 4, 5, 6, and 7), only the resorcin [4]arene 4 (n = 4) is accessible in high yield by the acid-catalyzed condensation of resorcinol and aldehydes.…”
Section: Common Classes Of Water-soluble Hostsmentioning
confidence: 99%
“…Protocols for replacing the tbutyl group of the upper rim (R = t-Bu) in the parent calixarenes, which is a necessary blocking group during the base-catalyzed condensation of the phenol and formaldehyde, are also well developed. The variability in n, R, and the phenol substituent provides a rich class of hosts with diverse applications, including sensing [104][105][106]. Although a variety of different-sized resorcinarenes have been reported (n = 4, 5, 6, and 7), only the resorcin [4]arene 4 (n = 4) is accessible in high yield by the acid-catalyzed condensation of resorcinol and aldehydes.…”
Section: Common Classes Of Water-soluble Hostsmentioning
confidence: 99%
“…Molecular recognition and inclusion complexation mechanism offer promising approaches for electrochemical sensing [27][28][29][30]45]. Calixarenes are cavity-shaped cyclic oligomers made up of phenol units linked via alkylidene groups [26,[46][47][48][49][50]. The lipophilic cavity of calixarene macromolecule provides a micro environment which an appropriately sized nonpolar drug molecule, or more often nonpolar parts, can enter to form an inclusion complex.…”
Section: Resultsmentioning
confidence: 99%
“…Conjugates of calix[n]arenes, in particular, the calix[4]arene, have been studied for their ion and molecular sensing aspects in solution owing to the ease of controlled derivatization of the platforms both at lower and upper rims . Variations in the induced supramolecular aggregation of the conjugates of calix[4]arenes by an ion or a molecule have been reported .…”
Section: Introductionmentioning
confidence: 99%