1993
DOI: 10.1021/jo00078a052
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Chlorosulfonylated calix[4]arenes: precursors for neutral anion receptors with a selectivity for hydrogen sulfate

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Cited by 136 publications
(71 citation statements)
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“…So, the design of anion receptors with high selectivity is challenging [9][10][11]. Synthetic receptors for anions are usually based on urea/thiourea [12,13], amides [14,15,25], macrocyclic ammonium/guanidinium [16,17], functionalized calixarenes [18,19], phenylhydrazone [20], indole [21] and -OH [26]. Take the phenylhydrazone for example, first, this kind of the receptor is neutral and the synthetic method is simple.…”
Section: Introductionmentioning
confidence: 99%
“…So, the design of anion receptors with high selectivity is challenging [9][10][11]. Synthetic receptors for anions are usually based on urea/thiourea [12,13], amides [14,15,25], macrocyclic ammonium/guanidinium [16,17], functionalized calixarenes [18,19], phenylhydrazone [20], indole [21] and -OH [26]. Take the phenylhydrazone for example, first, this kind of the receptor is neutral and the synthetic method is simple.…”
Section: Introductionmentioning
confidence: 99%
“…Among them there are a few examples of fluoroionophores based on peptidocalixarenes developed for anion recognition. Previously, we reported two cone calix [4]arene conformers which exhibited good recognition to F 2 and AcO 2 , respectively [28,29]. In this paper, we report another anion chemosensor based on a Nlinked peptidocalix [4]arene which showed selective fluorescent behavior of F 2 over other anions examined such as Cl 2 , Br 2 , I 2 , HSO 2 4 , NO 2 3 , AcO 2 and H 2 PO 2 4 .…”
Section: Introductionmentioning
confidence: 80%
“…They must be functionalized with suitable groups in order to make them soluble and relevant for studies in drug solubilization. Shinkai et al first reported the synthesis of water-soluble calix[n]arenes bearing sulfonate functional groups on the upper rim and alkyloxy groups on the lower rim [32][33][34][35]. The interior cavity of calix[n]arenes and calix [4]resorcinarenes in the cone conformation is typically hydrophobic and this can be exploited to form reversible host-guest complexes with small organic molecules via non-covalent interactions.…”
Section: Calix[n]arene Structurementioning
confidence: 99%