Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/22442
Title: Synthetic ionophores: Part 22 — Synthesis and ionophore behaviour of dioxadiamide-amine based macrocycles appended on binaphthol, biphenyl and calix[4]arene platforms†
Authors: Singh, Harjit
Sharma, Rajan
Malik, Vaishalli
Kumar, Subodh
Issue Date: Nov-2001
Publisher: NISCAIR-CSIR, India
Abstract: The diesters 3 and 4 prepared by o-alkylations of 1,1'-bi-2-naphthol and 2,2' dihydroxybiphenyl with ethyl chloroacetate and the 1,3-diester of calix[4]arene undergo aminolysis with diethylenetriamine and 3,3'-diaminodipropylamine to provide dioxadiamide-amine based macrocycles. Amongst these macrocycles calix[4]arene based macrocycle 10 shows moderate selectivity towards Pb2+ over alkali and alkaline earth metal cations.
Page(s): 1104-1107
URI: http://hdl.handle.net/123456789/22442
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.40B(11) [November 2001]

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