1999
DOI: 10.1002/(sici)1099-0518(19991201)37:23<4351::aid-pola11>3.0.co;2-l
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Synthesis and binding properties of calix[4]arene telomers

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Cited by 39 publications
(10 citation statements)
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“…From the results given in Table 1, it has been observed that oligomer 4a shows significant extraction ability toward alkali metal cations, whereas the other compounds (1-3) are ineffective for alkali metal cations in the liquid-liquid extraction systems (Fig. 1), and 4b can be a good adsorbent for alkali metal cations in the solid-liquid batchwise adsorption systems, very likely because of the structural and collective/cooperative behavior of thiacalix [4]arene moieties where the amide bridges and polymeric groups may also play an important role in this situation, which agreed with our previous results [33][34][35][36][37][38][39][40][41][42][43][44][45][46][47][48]. Table 2 shows that MerrifieldÕs polymer 5 is ineffective for alkali metal cations in the solid-liquid systems.…”
Section: Extraction Studiessupporting
confidence: 91%
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“…From the results given in Table 1, it has been observed that oligomer 4a shows significant extraction ability toward alkali metal cations, whereas the other compounds (1-3) are ineffective for alkali metal cations in the liquid-liquid extraction systems (Fig. 1), and 4b can be a good adsorbent for alkali metal cations in the solid-liquid batchwise adsorption systems, very likely because of the structural and collective/cooperative behavior of thiacalix [4]arene moieties where the amide bridges and polymeric groups may also play an important role in this situation, which agreed with our previous results [33][34][35][36][37][38][39][40][41][42][43][44][45][46][47][48]. Table 2 shows that MerrifieldÕs polymer 5 is ineffective for alkali metal cations in the solid-liquid systems.…”
Section: Extraction Studiessupporting
confidence: 91%
“…The solutions were then magnetically stirred in a thermostated water-bath at 25°C for 1 h, and finally left standing for an additional 30 min. The concentration of picrate ion remaining in the aqueous phase was then determined spectrophotometrically as previously described [39][40][41][42]. Blank experiments showed that no picrate extraction occurred in the absence of calixarene.…”
Section: Liquid-liquid Extraction Studiesmentioning
confidence: 99%
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“…These mechanisms are, in general, complicated because they may involve several different interactions [45,48,49]. Some of the reported interactions include: ion-exchange, complexation, coordination/chelation, electrostatic interactions, acidebase interactions, hydrogen bonding, hydrophobic interactions, and physical adsorption.…”
Section: Liquideliquid Extraction Studiesmentioning
confidence: 99%
“…The interesting properties shown by these cyclic oligomeric molecules stimulated the exploitation of useful methods towards their incorporation into polymeric matrices, which are interesting for the development of ion selective electrodes and membranes, chemical and biochemical sensors and selective extraction of ions and neutral molecules [15][16][17][18][19]. Previously, to increase the affinity of calixarenes toward metal ions and anions, two main strategies have been followed: first, different ionophoric groups including carbonyl, amide, and nitrile have been incorporated onto the calixplatform; second, the calixarene units have been fixed in a polymeric matrix [20][21][22][23][24][25][26][27][28][29]. We have also reported the synthesis of calix(aza)crowns and their corresponding oligomers along with their extraction behavior towards toxic metal cations [30].…”
Section: Introductionmentioning
confidence: 99%