2007
DOI: 10.1016/j.tet.2007.03.138
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Synthesis and dichromate anion extraction ability of p-tert-butylcalix[4]arene diamide derivatives with different binding sites

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Cited by 42 publications
(14 citation statements)
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“…In our previous study [27,40,41], we report the synthesis and extraction studies of polymers based on a calix [4]arene platform with cyclic amino groups on their upper rim. It was observed that the ionophores were very good adsorbents for dichromate from aqueous solution.…”
Section: Dichromate Anion Sorption Studiesmentioning
confidence: 99%
“…In our previous study [27,40,41], we report the synthesis and extraction studies of polymers based on a calix [4]arene platform with cyclic amino groups on their upper rim. It was observed that the ionophores were very good adsorbents for dichromate from aqueous solution.…”
Section: Dichromate Anion Sorption Studiesmentioning
confidence: 99%
“…Nevertheless, since the periphery of the anions has oxide moieties, these are potential sites for hydrogen. The maximum permissible levels of Cr(VI) in potable and industrial wastewaters are 0.05 and 0.25 mg/L, respectively [12]. Due to its high solubility, Cr(VI) is very toxic to living organisms compared to Cr(III) [13].…”
Section: Introductionmentioning
confidence: 99%
“…Compounds 1-4 were synthesized according to previously published procedures [17], whereas compounds 5 and 6 were synthesized according to the route shown in Scheme 1. Briefly, a solution of 1-(2-furoyl)piperazine or 1-(2-pyrimidyl)piperazine (21.76 mmol) in tetrahydrofuran (THF, 25 mL) was added to a solution of 25,27-bis(chlorocarbonylmethoxy)-26,28-hydroxycalix [4]arene (4) (6.2 g, 5.44 mmol) in THF (100 mL) in a drop-wise manner over 1 h with continuous stirring at room temperature, and the resulting mixture was stirred at the same temperature for 5 h. The solvent was then removed in vacuo to give a residue, which was dissolved in water (200 mL) and neutralized (pH 7) by the addition of 0.1 M HCl.…”
Section: Synthesismentioning
confidence: 99%
“…All of the newly synthesized compounds were characterized by 1 H and 13 C NMR, FT-IR and elemental analyses. Compounds 1-4 were synthesized according to previously published procedures [17]. Compounds 5 and 6 were synthesized from the corresponding acid chlorides.…”
Section: Synthetic Routesmentioning
confidence: 99%